Wisp1 is a circulating factor that stimulates proliferation of adult mouse and human beta cells

Fernandez-Ruiz, Rebeca; García-Alamán, Ainhoa; Esteban, Yaiza; Mir-Coll, Joan; Serra-Navarro, Berta; Fontcuberta-PiSunyer, Marta; Broca, Christophe; Armanet, Mathieu; Wojtusciszyn, Anne; Kram, Vardit; Young, Marian F.; Vidal, Josep; Gomis, Ramon; Gasa, Rosa

doi:10.1038/s41467-020-19657-1

Download PDF

Article
Open access
Published: 25 November 2020

Wisp1 is a circulating factor that stimulates proliferation of adult mouse and human beta cells

Rebeca Fernandez-Ruiz^1,2,3,
Ainhoa García-Alamán^1,2,
Yaiza Esteban^1,2,
Joan Mir-Coll^1,3,
Berta Serra-Navarro^1,3,
Marta Fontcuberta-PiSunyer¹,
Christophe Broca⁴,
Mathieu Armanet⁴,
Anne Wojtusciszyn^4,5,
Vardit Kram⁶,
Marian F. Young⁶,
Josep Vidal^1,2,7,
Ramon Gomis^1,2,3,8 &
…
Rosa Gasa ORCID: orcid.org/0000-0001-5639-5441^1,2

Nature Communications volume 11, Article number: 5982 (2020) Cite this article

4375 Accesses
22 Citations
17 Altmetric
Metrics details

Subjects

Diabetes

Abstract

Expanding the mass of pancreatic insulin-producing beta cells through re-activation of beta cell replication has been proposed as a therapy to prevent or delay the appearance of diabetes. Pancreatic beta cells exhibit an age-dependent decrease in their proliferative activity, partly related to changes in the systemic environment. Here we report the identification of CCN4/Wisp1 as a circulating factor more abundant in pre-weaning than in adult mice. We show that Wisp1 promotes endogenous and transplanted adult beta cell proliferation in vivo. We validate these findings using isolated mouse and human islets and find that the beta cell trophic effect of Wisp1 is dependent on Akt signaling. In summary, our study reveals the role of Wisp1 as an inducer of beta cell replication, supporting the idea that the use of young blood factors may be a useful strategy to expand adult beta cell mass.

The type 1 diabetes gene TYK2 regulates β-cell development and its responses to interferon-α

Article Open access 26 October 2022

Vikash Chandra, Hazem Ibrahim, … Timo Otonkoski

Pronounced proliferation of non-beta cells in response to beta-cell mitogens in isolated human islets of Langerhans

Article Open access 28 May 2021

Hasna Maachi, Julien Ghislain, … Vincent Poitout

Targeted pharmacological therapy restores β-cell function for diabetes remission

Article 20 February 2020

Stephan Sachs, Aimée Bastidas-Ponce, … Heiko Lickert

Introduction

Loss of functional beta cell mass is a central feature in the pathogenesis of diabetes, and restoration of the beta cell mass reservoir through replication of remaining beta cells has been envisioned as a potential therapeutic strategy to treat this disease. This has fueled a growing interest in deciphering the molecular pathways that direct beta cell proliferation and increasing efforts to identify exogenous factors that can be used to promote beta cell replication in situ and in vitro.

The main mechanism by which beta cells expand themselves is through replication, but their ability to proliferate declines with age, and, therefore, adult beta cells are considered resistant to different proliferative stimuli¹. In the mouse, beta cell replication is high in the late embryonic and perinatal periods and progressively diminishes until reaching low levels after weaning. Several studies indicate that intrinsic changes in beta cells, such as an age-dependent increase in p16^INK4A, a cyclin-dependent kinase inhibitor, restrict the proliferation of both old mouse and human beta cells². Likewise, loss of islet responsiveness to platelet-derived growth factor (PDGF) signaling due to down-regulation of the expression of PDGF receptors has been associated to the decline in beta cell proliferation after birth³.

As it has been shown for other cell types, the age-dependent decrease in beta cell proliferation not only depends on intrinsic molecular changes, but it is also the consequence of modifications of the systemic environment that cells are exposed to^4,5,6. In this regard, parabiosis experiments in mice demonstrated that old beta cells regain the ability to proliferate when they are exposed systemically to blood from young mice⁷. Despite the growing body of research on molecules that can act as beta cell trophic factors in vitro and/or in vivo^8,9,10,11, the nature of the factor/s present in young blood that function as stimulators of beta cell growth remains elusive.

Matricellular proteins are nonstructural proteins present in the extracellular cellular matrix that, rather than having stable structural roles, tend to exhibit rapid turnover and play dynamic roles in multiple cellular processes, including cell proliferation, programmed cell death, extracellular matrix production or cellular migration¹². These proteins exhibit a largely context-specific mode of action based on their ability to interact with multiple partners, including major structural elements in the matrix, specific cell surface receptors and growth factors. Among these matricellular proteins, there is the CCN protein family¹³. There are six CCN proteins, designated CCN1 to CCN6, which share a modular structure comprised of a signal peptide followed by three domains with homology to insulin-like growth factor binding protein, von Willebrand type C and thrombospondin type 1 repeat, plus a fourth domain which contains a cysteine-knot motif¹⁴. This modular structure underlies the pleiotropic functions and cell-specific behavior of this family of proteins, as CCN proteins can use different cell-surface receptors in different cell types to interact with multiple partners present in the surrounding extracellular matrix¹⁵. Two members of the CCN family, CCN1/Cyr61 and CCN2/CTGF, are expressed in the pancreas where they have been associated with proliferative processes. On one hand, upregulation of CCN1/Cyr61 in pancreatic carcinoma cells alters expression of genes encoding MAPK/ERK and PI3K and stimulates cell division in response to growth factors¹⁶. On the other hand, CCN2/CTGF is expressed in mouse embryonic beta cells and re-expressed in adult beta cells during periods of expansion such as pregnancy or after high fat feeding¹⁷.

CCN4/Wisp1 (Wnt-1 inducible signaling protein 1) was first identified as a target of the Wnt pathway in mammary epithelial cells¹⁸. Wisp1 was subsequently found to be expressed in multiple sites within the body and to be involved in a broad spectrum of biological functions and pathological processes. Thus, Wisp1 participates in development, tumorigenesis and tissue repair through regulation of apoptosis, adhesion, migration, differentiation, and proliferation processes^19,20,21. In the musculoskeletal system, Wisp1 is produced by osteoblasts and their precursors and has been shown to be pivotal for osteoblastic differentiation during bone development²², and to assist with fracture repair²³ and growth plate cartilage injury²⁴. Wisp1 has also been described as a pro-inflammatory adipokine²⁵. Its expression in adipose tissue is lowered by diet-induced weight loss in human subjects, whilst it augments in response to high fat diet feeding in mice^25,26. Furthermore, circulating levels of WISP1 and WISP1 expression in visceral adipose tissue were found increased in obesity, irrespective of type 2 diabetes status, and associated with insulin resistance and adipose tissue inflammation^27,28.

In the present study, we aimed at identifying blood factors present in pre-weaning stages that may contribute to high rates of beta cell proliferation during this period. Using antibody arrays, we identified Wisp1 as a protein enriched in serum from lactating as compared to adult mice. Because the role of Wisp1 in beta cell physiology has not been previously addressed, here we sought to investigate the potential of Wisp1 as a beta cell trophic factor.

Results

Adult beta cells exhibit enhanced proliferation when transplanted into pre-weaning mice

We first examined whether a young environment could increase the proliferation of adult beta cells. To this aim, we performed syngeneic transplants of islets isolated from 20-week-old (20wo) C57BL6/J mice into the anterior chamber of the eye (ACE) of adult or postnatal day 16 (p16) C57BL6/J recipients. We found that, 12-days post-transplantation, the proportion of proliferating beta cells, both counting cells positive for the proliferation marker ki67 (marks cells engaged in the cell cycle) or for the marker of cellular mitosis pHH3 (phosphorylated histone H3), were higher in the grafts implanted in p16 relative to 20wo recipients (Fig. 1a–c). To overrule age-associated changes in graft vascularization that could have influenced this result, we performed immunostaining against CD31/PECAM-1, a vascular marker, and in vivo confocal imaging of blood vessels using rhodamine dextran. As illustrated in Supplementary Fig. 1 and Supplementary Movies 1–6, there were no obvious differences in vascularization between p16 and adult eye grafts. Next, we transplanted human islets isolated from adult individuals (55 and 56 years of age) into the ACE of immunocompromised p16 or 20wo NSG-SCID mice. Similar to their mouse counterparts, human beta cells proliferated more (as indicated by ki67 and pHH3 staining) when transplanted into young relative to adult mouse recipients (Fig. 1d–f). Together, these experiments support the notion that the young circulatory systemic environment stimulates the proliferation of adult mouse and human beta cells.

**Fig. 1: Adult beta cells exhibit enhanced replication when transplanted into pre-weaning mice.**

Identification of Wisp1 as a factor enriched in pre-weaning mouse serum

The above results prompted us to search for beta cell trophic factors present in young blood that could stimulate adult beta cell proliferation. Using commercial antibody arrays that covered a total of 365 different proteins, we compared serum from p14 and 20wo mice. Applying a 2-fold cut-off, 17 proteins appeared to be more abundant in young than in adult serum (Supplementary Fig. 2). Some of the identified factors had been previously associated with beta cell growth, survival or function, including MCP-1²⁹, Igf-1^30,31, osteopontin^32,33, and osteoprogeterin³⁴. However, because all these proteins can be produced by islets^29,32,34,35, they could not be genuinely regarded as extrinsic factors.

The CCN family protein CCN4/Wisp1 was also found enriched in p16 relative to 20wo serum (Fig. 2a). No information on the role of Wisp1 in pancreatic beta cells was available and hence we sought to interrogate the potential function of Wisp1 as a beta cell trophic factor. As an initial experiment we validated the array results with an ELISA specific for mouse Wisp1. We measured serum Wisp1 concentrations in mice of different ages (from p14 to 20wo) and confirmed an age-dependent decrease in circulating Wisp1 levels, which dropped nearly 6-fold between pre-weaning and adult stages (Fig. 2b). To corroborate these findings in humans, we measured circulating WISP1 with an ELISA specific for human WISP1 in blood from children aged 2–5 years and adults aged 28–45 years. Remarkably, in concordance with our results in mice, WISP1 levels dropped 3-fold between child and adult stages (Fig. 2c).

**Fig. 2: Identification of Wisp1 as a factor enriched in blood of pre-weaning mice.**

Prior to investigating the role of Wisp1 in beta cells, we sought to ascertain the extrinsic nature of any potential effect of Wisp1 in islets. With this aim, we examined Wisp1 gene expression in islets isolated from pre-weaning and adult mice. Wisp1 transcript levels were negligible at either age thus discarding any potential role of Wisp1 as an intrinsic regulator (Fig. 2d). On the contrary, transcripts for the CCN genes Cyr61 and Ctgf were readily detectable in mouse islets at both ages (Fig. 2d). Importantly, a similar expression pattern was observed in adult human islets (Fig. 2e).

To identify the tissue source of Wisp1 in suckling mice, we determined Wisp1 mRNA levels in several p14 mouse tissues. Among them, bone displayed the highest Wisp1 gene expression levels followed by lung and skeletal muscle. Wisp1 mRNA levels decayed in adult bone reaching values closer to the other surveyed tissues (Fig. 2f). Using immunohistochemistry, we found increased Wisp1 staining in young versus adult bone tissue (Supplementary Fig. 3). Corroborating this finding, calvaria bone cells isolated from young mice secreted more Wisp1 than those isolated from adult mice (Supplementary Fig. 3). Thus, these evidence indicate that the bone is the likely source of circulating Wisp1 in pre-weaning mice.

Wisp1 contributes to proliferation of endogenous and transplanted beta cells in young mice

To study the involvement of Wisp1 in beta cell proliferation during early postnatal life, we performed three experiments using mice with constitutive deletion of the Wisp1 gene (Wisp1⁻/⁻). First, we studied endogenous beta cell proliferation in fixed pancreatic tissue and found that beta cell staining of ki67 and pHH3 were both reduced in p14 Wisp1⁻/⁻ mice as compared to their wild-type (Wisp1⁺/⁺) littermates (Fig. 3a–c). Circulating levels of Igf-1 and osteopontin were comparable whilst osteoprogeterin levels were modestly reduced (17%) in p14 Wisp1⁻/⁻ as compared to their Wisp1⁺/⁺ littermates (Supplementary Fig. 4a–c), indicating that the effects of Wisp1 ablation on beta cell proliferation are unlikely secondary to alterations in these factors.

**Fig. 3: Wisp1 contributes to beta cell replication in young mice.**

Second, we determined if administration of recombinant mouse Wisp1 (rmWisp1) to Wisp1⁻/⁻ animals could enhance postnatal beta cell proliferation in vivo. To this aim, three intraperitoneal injections of rmWisp1 or saline were dispensed to Wisp1⁻/⁻ pups for three consecutive days, from p9 to p11. At p12, Wisp1⁻/⁻ pups that had received rmWisp1 presented proliferation rates that were 1.7–2 fold higher than those of littermate Wisp1⁻/⁻ that had received saline (Fig. 3d–f). Note that proliferation rates in these latter group were higher than those reported for p14 Wisp1⁻/⁻ pups (Fig. 3a, b), consistent with the rapid drop in beta cell proliferation that occurs during the first postnatal weeks^36,37. No changes in Igf-1, osteoprogeterin or osteopontin were observed in mice treated with rmWisp1 as compared to saline controls (Supplementary Fig. 4d–f).

Third, to evaluate the contribution of Wisp1 to the replication of adult beta cells transplanted into young mice (Fig. 1), we performed new transplants using p16 Wisp1⁻/⁻ mice as recipients. We observed that beta cells of transplanted adult mouse islets proliferated less (50%) when implanted in Wisp1⁻/⁻ relative to islets implanted in p16 Wisp1⁺/⁺ littermates (Fig. 3g–i); and this was not due to differences in functional vascularization of the islet grafts between genotypes (Supplementary Movies 7–10).

Altogether, these results support the pro-proliferative role of Wisp1 in beta cells of pre-weaning mice.

Wisp1 enhances beta cell proliferation and beta cell mass expansion in adult mice

We next queried whether Wisp1 could promote proliferation of beta cells in adult mice. To overexpress this protein systemically, we administered adenoviral particles encoding the human isoform of WISP1 (Ad-WISP1) via tail vein injection to adult mice. As control, we injected a recombinant adenovirus encoding beta-galactosidase (Ad-betaGal). Human WISP1 transcripts were readily detected by qPCR in the liver at days 7 and 14 post-administration of Ad-WISP1 (Fig. 4a). Hepatic mRNA levels of the mouse Wisp1 gene were not changed by transgenic expression of WISP1 (Fig. 4b). Using an ELISA specific for human WISP1, we confirmed the presence of the human protein in serum from mice injected with Ad-WISP1 but not in mice injected with Ad-betaGal (Fig. 4c). We then monitored the number of ki67-positive beta cells and observed that, 7 days after the adenoviral injection, mice receiving Ad-WISP1 presented higher beta cell proliferation as compared to mice receiving Ad-betaGal (Fig. 4d, e). This rise in beta cell replication resulted in a modest increase in beta cell mass 14 days post-injection of Ad-WISP1 (Fig. 4f), which did not have effects in either body weight or whole-body glucose tolerance (Supplementary Fig. 5).

**Fig. 4: Adenovirus-mediated expression of Wisp1 enhances endogenous beta cell proliferation in adult mice.**

We then investigated the potential of Wisp1 to promote beta cell proliferation in a pathological setting. To this aim, we administered Ad-WISP1 or Ad-betaGal to Stz-induced diabetic adult mice (Fig. 5a). Human WISP1 transcripts were detected in the liver 14 days post-injection with Ad-WISP1 without accompanying changes in endogenous Wisp1 transcripts (Fig. 5b). The presence of human WISP1 in serum of Ad-WISP1 injected mice was confirmed at days 9 and 14 post-viral injection (Fig. 5c). Systemic overexpression of WISP1 did not normalize Stz-induced hyperglycemia during the follow-up period, even though there was a trend to lower glucose levels (Fig. 5d). However, at day 14 after injection with Ad-WISP1, mice exhibited a significant increase in ad lib fed plasma insulin levels as compared to animals injected with Ad-betaGal (Fig. 5e). This change was not associated with amelioration of whole-body glucose tolerance or glucose-induced insulin secretion in Ad-WISP1-injected mice (Supplementary Fig. 6). Yet, detailed morphometric assessment of the pancreatic beta cell compartment revealed a nearly two-fold increase in proliferating beta cells in animals treated with Ad-WISP1 relative to controls (Fig. 5f, g). In line with enhanced proliferation, we found increased insulin-positive area and total beta cell mass (Fig. 5h, i).

**Fig. 5: Adenovirus-mediated expression of Wisp1 promotes endogenous beta cell proliferation in adult diabetic mice.**

Collectively, these experiments confirm that circulating WISP1 can increase the proliferation of pancreatic beta cells in situ in adult animals, further supporting the potential of this protein as a beta cell trophic factor.

Wisp1 stimulates mouse and human beta cell proliferation in vitro

All of the preceding experiments were performed using in vivo models. Here, we sought to investigate if Wisp1 could induce adult beta cell proliferation directly, in the absence of other systemic factors. First, we treated adult mouse islets ex vivo for 2 days with different concentrations of recombinant mouse Wisp1 (rmWisp1) protein and determined the percentage of ki67-positive beta cells. As shown in Fig. 6a, rmWisp1 induced a a dose-dependent rise in beta cell proliferation, with a maximum 2.4-fold increase observed at 500 ng/ml rmWisp1 relative to control values. The effect of rmWisp1 was compared to that of the small molecule harmine, a DYRK1A inhibitor and c-myc activator³⁸. Correlating with previous studies^38,39, harmine promoted a dramatic increase in mouse beta cell proliferation, reaching values 4-fold higher than with rmWisp1 (Fig. 6a, b).

**Fig. 6: Wisp1 promotes mouse beta cell replication in vitro.**

Recombinant factor-based assays typically require supra-physiological amounts of protein to maintain effective concentrations; hence we performed a second experiment to validate the mitogenic effect of physiological quantities of Wisp1. To this aim, we treated NIH3T3 cells with Ad-WISP1 or Ad-betaGal and then co-cultured them with adult mouse islets for 24 h or 48 h. In this experiment the achieved concentration of human WISP1 in the culture media (3–6 ng/ml) was in the same order of magnitude than endogenous Wisp1 in mouse serum (Supplementary Fig. 7). Consistent with experiments with rmWisp1, beta cells in mouse islets exposed to NIH3T3/Ad-WISP1 presented enhanced ki67 labeling as compared to beta cells in islets co-cultured with NIH3T3/Ad-betaGal (Fig. 6c, d). In agreement with this observation, islets exposed to NIH3T3/Ad-WISP1 had increased expression of known Wisp1 gene targets such as Axin2 or Ndrg1/3 and of the cell cycle genes Foxm1 and Plk1 (Supplementary Fig. 7).

Human beta cells have an apparent lower replicative potential than mouse beta cells, and different factors described in the literature as inducers of beta cell replication in rodents have been reported to exert modest or no effect in human beta cells. Thus, we interrogated the proliferative effects of recombinant human WISP1 (rhWISP1) in human islets. A two-day treatment with rhWISP1 increased dose-dependently the percentage of doubly positive ki67/insulin cells (Fig. 6e, f). Remarkably, the effectiveness of rhWISP1 was comparable to that of harmine in human islets (Fig. 6f), reaching proliferation values of ∼2% similar to those described for human beta cells during the first year of life⁴⁰. The reduced effectiveness of harmine in human as compared to mouse islets has been previously reported^38,39.

Wisp1 acts via AKT to stimulate mouse and human beta cell proliferation in vitro

Akt/PKB has been postulated as the intracellular mediator of Wisp1 actions in several cellular contexts^41,42. To address the involvement of Akt in Wisp1-induced beta cell proliferation, we first determined levels of Ser473 phosphorylation of this kinase (active form) in mouse islets using immunoblot analysis. Incubation with rmWisp1 significantly increased phospho-Akt levels (Fig. 7a), thus corroborating that this kinase is a downstream target of Wisp1 in islets. Furthermore, chemical inhibition of Akt impaired Wisp1-induced beta cell proliferation (Fig. 7b, c), proving the involvement of Akt in the pro-proliferative actions of Wisp1.

**Fig. 7: Wisp1 activates Akt in mouse and human pancreatic islets.**

Finally, we queried whether Akt was also required for the mitogenic effect of Wisp1 in human islets. Like their mouse counterparts, incubation with rhWISP1 augmented AKT phosphorylation in human islets and chemical inhibition of this kinase blocked WISP1-triggered increase in the number of ki67+ human beta cells (Fig. 7d, e).

Together, these results support that Akt mediates the pro-proliferative effects of Wisp1 in mouse and human beta cells.

Discussion

This study supports the involvement of systemic factors in the decline of beta cell proliferation during normal organism growth. Our present results parallel prior parabiosis experiments showing that circulating factors in young adult mice (1-month old) increased beta cell proliferation rates in older mice (8 months old)⁷. Here, by grafting mouse and human islets in the eye, we demonstrate the existence of systemic factors in pre-weaning mice, a time when beta cell replication is highly active, that can stimulate adult beta cell proliferation. These observations add to an emerging body of evidence showing the regenerative capacity of young blood in other organs such as skeletal muscle⁴³, heart⁴⁴ and brain⁴⁵. In our search of serum proteins contributing to high beta cell proliferation rates in suckling pups, we identified Wisp1 as a factor whose abundance in circulation drops after weaning in mice. Notably, we found that circulating WISP1 levels were also higher in children than in adults, revealing an analogous age-dependent decline of this factor in both species.

We found the bone as the tissue exhibiting highest Wisp1 gene expression levels in suckling mice and confirmed higher production of Wisp1 by young than adult bone. These observations are in agreement with the reported involvement of Wisp1 in the regulation of skeletal remodeling and bone structure²² and the profound changes in skeletal metabolism that occurs in suckling pups, as bone formation takes place mostly during embryonic development and postnatal growth⁴⁶. In fact, the skeleton is no longer recognized only as a mechanical scaffold, but also as an endocrine organ which regulates glucose metabolism and energy expenditure^47,48. It is also known to secrete humoral factors that affect beta cell mass, such as osteopontin³², osteoprotegerin³⁴, and osteocalcin⁴⁹. Remarkably, we found that both osteopontin and osteoprotegerin were increased in serum of pre-weaning mice, reinforcing the notion that bone produces blood-borne factors that participate in early postnatal beta cell mass expansion.

It will be interesting to determine whether Wisp1 is involved in known conditions of enhanced adult beta cell proliferation, such as insulin resistance and obesity. Intriguingly, Wisp1 has been recently described as an adipokine whose levels negatively correlate with insulin sensitivity²⁵, although no differences in circulating Wisp1 levels have been reported between normal, impaired glucose tolerant and diabetic human subjects⁵⁰. We have examined serum Wisp1 levels in mice fed a high fat diet (HFD) and found a rather modest increase (~2-fold) after 10 day HFD feeding, but no differences after 60 or 120 day HFD feeding (Supplementary Fig. 8), indicating that, if any, the role of Wisp1 might be limited to the reported initial activation of beta cell proliferation in response to HFD⁵¹.

One central result of this study is that Wisp1 promotes proliferation of human beta cells, which are considered refractory to the mitogenic actions of many factors that exert robust pro-proliferative effects in mouse beta cells. Nonetheless, from a therapeutic standpoint, the existing studies that report mitogenic effects of Wisp1 in various cell types^{20,41,52,53,54}, raise concerns about its specificity and the risk that systemic administration of this factor might have undesirable effects in extra-pancreatic tissues. Yet, it has been described that Wisp1 does not signal through a unique specific receptor but it rather acts by modulating other growth factor signaling pathways⁵⁵, making Wisp1 actions dependent not only on intrinsic cues of its target cell but also on the specific extracellular context where it acts. Thus, combination of Wisp1 with other factors might be the key to provide enhanced specificity towards beta cells. For instance, in agreement with reports in other cellular contexts^41,56, here we show that Wisp1 activates Akt in mouse and human islets. That Akt activation induces beta cell proliferation has been previously established^57,58. Yet, this effect is often connected with its function as a central mediator of the Insulin/IGF signaling pathway, which is an important regulator of beta cell growth^59,60,61. Therefore, it is tempting to speculate that Wisp1 might act synergistically with ligands of the Insulin/IGF pathway to activate beta cell proliferation via modulation of Akt activity. Future studies should be aimed at addressing the beta cell trophic effects of this and other possible factor combinations.

In conclusion, our study identifies Wisp1 as a circulating protein that is abundant in young blood and induces proliferation of adult beta cells, thus revealing Wisp1 as an agent with potential therapeutic use to expand beta cell mass in diabetes. This work lays the background for further studies aimed at identifying circulating factors present in early postnatal life that can be used as therapeutic agents to expand beta cell mass in adulthood.

Methods

Animals

C57BL6/J, immunocompromised NSG-SCID (Jackson Laboratories) and Wisp1 knockout mice (Wisp1^−/−)²² were bred at the barrier animal facility of the University of Barcelona. Wisp1⁻/⁻ mice were genotyped with primers provided in Supplementary Table 1. Animals were maintained in a 12-h light/12-h dark cycle in temperature and humidity-controlled environment with free access to water and standard laboratory chow. All adult mice used in the experiments were male. Pre-weaning mice were both male and female.

Diabetes was induced in 4–6 h fasted 12–16 week-old C57BL6/J male mice by a single intraperitoneal injection of 125 mg/Kg streptozotocin (Stz, Sigma-Aldrich, St Louis, MO, USA) diluted in 0.9% NaCl with 100 mmol/l sodium citrate (pH 4.5). Mice that had plasma blood glucose concentrations above 300 mg/dl for three consecutive days were considered for the experiment.

Antibody arrays

Serum samples were individually obtained by centrifugation of the whole blood at 8000 × g for 15 min twice. Three different p14 and 20wo serum batches (each a pool from 6 animals) were analyzed using the RayBio Mouse Cytokine Antibody Array Kit (Raybiotech, Inc. Georgia, USA) and Proteome Profiler^TM Array/Mouse XL Cytokine Array Kit (R&D Systems, Minneapolis, USA) following manufacturer’s instructions. Membranes were scanned using a LAS4000 Lumi-Imager (Fuji Photo Film, Valhalla, NY) and analyzed using ImageJ/Fiji software. The results were then normalized using internal controls, and the relative protein abundance in p14 compared to adult mouse serum was represented.

Islet isolation and culture

Donor mouse islets were obtained from C57BL6/J male mice with ages ranging from 12 to 20 weeks by collagenase digestion and Histopaque gradient purification as previously described⁶². Isolated islets were allowed an overnight recovery in RPMI-1640 media with 11 mM glucose, 10% FBS and antibiotics before performing experiments.

Human islets were obtained from 8 cadaveric donors (males and females) with an average age of 54.1 ± 3.7 years and BMI of 24.7 ± 1.4 kg/m². Isolated islets were prepared by collagenase digestion followed by density gradient purification at the Laboratory of Cell Therapy for Diabetes (Hospital Saint-Eloi, Montpellier, France), as previously described⁶³. After reception, human islets were maintained in culture for 1–3 days in RPMI-1640 with 5.5 mM glucose, 10% fetal bovine serum (FBS) and antibiotics, before performing the experiments.

Transplant into the anterior chamber of the eye

Groups of 100-150 mouse or human islets were introduced and allowed to deposit at the bottom of a polythene cannula (Fine Bore Polythene Tubing, Smiths Medical International). Recipient mice (C57BL6/J, Wisp1^+/+, Wisp1^−/− or NSG-SCID) were anesthetized with ketamine-xylacine (100 mg/Kg body weight Ketamine+10 mg/ Kg body weight Xylacine), and islets were introduced in the anterior chamber of the eye under a stereomicroscope, using a Hamilton syringe. Viscofresh (10 mg/ml sodium carmellose) was used to relieve eye discomfort when the mice recovered from the anesthetics. Twelve days after implantation, mice were euthanized and eyes were removed and processed for subsequent immunofluorescence analysis.

Functional graft vascularization was assessed as described⁶⁴. In brief, mouse islets were labeled with 10 μM CFDA SE (Vybrant® CFDA SE Cell Tracer Kit, Invitrogen^TM, Molecular Probes®) for 15 min at 37 °C. Mice were anesthetized with Ketamine (100 mg/kg)-Xylazine (10 mg/kg), and 80 mg/Kg body weight of rodamine dextrane (Rhodamine B Isothiocyanate-Dextran, Sigma) was administered intraocularly. Live observation of blood vessels in the anterior chamber of the eye was carried out under a Leica TCS SP5 resonant scan spectral confocal microscope (Leica Microsystems Heidelberg GmbH) equipped with an incubation system with temperature control, a HCX IR APO L 25× water immersion objective (Numerical Aperture 0.95), resonant scanner at 8000 lines/s and blue diode (405 nm), Argon (488 nm) and diode pumped solid state (561 nm). Fluorescent dyes CFDA SE and Dextran-Rhodamine were acquired simultaneously using 488 and laser lines, AOBS (Acoustic Optical Beam Splitter) as beam splitter and emission detection ranges 500–550 nm and 571–625 nm, respectively and the confocal pinhole set at 4 Airy units. Z sectioning was performed every 300 nm to reconstruct whole islet.

In vivo adenoviral treatment

The recombinant adenovirus encoding full-length human WISP1 (Ad-WISP1) and the control adenovirus encoding beta galactosidase (Ad-betaGAL) were described elsewhere^65,66. Adenoviruses were purified and titrated by the Viral Vector Production Unit of the University Autonomous of Barcelona. Recombinant adenoviruses (2.45xE9 pfu) were injected into the tail vein of both control and diabetic C57BL6/J mice. Blood glucose was regularly monitored in diabetic mice after viral injection. At the time of sacrifice, pancreases were harvested and processed for immunofluorescence staining.

In vivo assessment of glucose homeostasis

The Intraperitoneal Glucose Intolerance Test (ipGTT) was performed after 5–6 h of food deprivation by administration of an intraperitoneal injection of D-glucose (2 g/Kg body weight). Glucose in tail vein blood was measured at the indicated time points after injection using a clinical glucometer and Accu-Check test strips (Roche Diagnostics, Switzerland). Plasma samples were obtained by blood centrifugation and kept at −80 °C for subsequent insulin determination by ELISA.

Gene expression analysis

Total RNA was isolated from mouse tissues using TRI Reagent® (Sigma-Aldrich, Missouri, USA) and from isolated islets using the NucleoSpin XS RNA kit (Mackerey-Nagel, Düren, Germany). First-strand cDNA was prepared using the Superscript III RT kit and random hexamer primers (Invitrogen, Carlsbad, CA, USA). Reverse transcription reaction was carried for 90 min at 50 °C and an additional 10 min at 55 °C. Real time quantitative PCR (qPCR) was performed on an ABI Prism 7900 sequence detection system using GoTaq® qPCR Master Mix (Promega Biotech Ibérica, Alcobendas, Madrid, Spain). Expression relative to the housekeeping gene Tbp was calculated using the deltaCt method. Primer sequences are provided in Supplementary Table 1.

Immunofluorescence staining and morphometric analysis

Pancreases and eyes were harvested, fixed overnight in 10% formalin and 2% paraformaldehyde, respectively, and subsequently washed, dehydrated and embedded in paraffin wax. For immunofluorescence in paraffin sections, a standard immunodetection protocol was followed as described elsewhere⁶⁷. Briefly, tissues were rehydrated and, when required, subject to heat-mediated antigen retrieval in citrate buffer. After a blocking step in 5% donkey or goat serum, and permeabilization using 1% (v/v) Triton X-100, tissue sections were incubated overnight with primary antibodies and then for 1 h with fluorescent-labeled secondary antibodies (Supplementary Table 2). For beta cell morphometric analysis, at least six non-consecutive (<150 µm apart) 4 µm thick sections were analyzed per pancreas. Beta cell fractional area was quantified as insulin-positive area relative to total pancreatic area. Beta cell mass was calculated as beta cell fractional area multiplied by pancreas weight. Beta cell proliferation was expressed as the percentage of cells doubly stained for insulin/ki67 or insulin/phosho-histone H3 (pHH3) relative to total number of insulin-positive cells, and at least 1500–3000 beta cells per animal were counted. Vascularization in transplanted islet grafts was calculated as the percentage of CD31+ area relative to insulin+ area.

For in toto immunofluorescence, whole islets were fixed in 4% paraformaldehyde for 30 min, washed with PBS, permeabilized in PBS-0.5% Triton X-100 and blocked in PBS-10% FBS-0.5% Triton X-100. Subsequently, islets were incubated overnight with primary antibodies and then for 2 h with fluorescent-labeled secondary antibodies (Supplementary Table 2). Nuclei were stained with Hoechst 33258 (Sigma). Fluorescent images were captured using a Leica TCS SPE confocal microscope, collected with Leica LAS AF v2.7.3.9723 and subsequently analyzed using Image J v1.50d software (Wayne Rayband, National Institutes of Health, http://rsb.info.nih.gov/ij/). For quantification of beta cell proliferation, the number of cells doubly positive for insulin and ki67 or pHH3 was analyzed in Z stacks 10 μm apart in order to avoid counting the same cell twice.

NIH3T3 and mouse islet co-culture

NIH-3T3 cells were grown in DMEM-4.5 g/L glucose (Sigma-Aldrich, St Louis, MO, USA) plus 10% Calf Serum and antibiotics. For adenoviral infection, NIH-3T3 cells were seeded onto 12-well plates (2.5xE4 cells/well) and incubated one day later with Ad-WISP1 or Ad-betaGal at a multiplicity of infection (moi) of 25 for 6 h. 12–16 h after virus removal, cells were co-cultured with mouse islets isolated the previous day. Co-cultures were performed in transwell culture inserts consisting of 0.4 µm translucent pet membrane (BDFalcon) using RPMI-1640 plus 8 mM glucose and 5% FBS. Following 24 and 48 h of co-culture, medium was collected for ELISA and islets were recovered for total RNA extraction and for in toto immunofluorescence staining to quantify proliferation.

Recombinant Wisp1 protein

Recombinant mouse Wisp1 and human WISP1 proteins were purchased from R&D Systems. Isolated mouse or human islets were cultured in RPMI-1640 plus 8 mM glucose and 5% FBS with or without the indicated recombinant proteins alone or with the Akt inhibitors AZD5363 (5 μM, Selleckchem) and Akti-1/2 (10 μM, Abcam) during the times indicated. Islets were then recovered for subsequent in toto immunofluorescence staining and immunoblot analysis.

For in vivo Wisp1 treatment, mouse recombinant mouse Wisp1 protein was administered daily by intraperitoneal injection at 1 mg/Kg body weight per day to Wisp1^−/− pups from p9 to p11. At p12, one day after last injection, animals were anesthetized and blood samples and pancreases were stored for subsequent analysis of circulating recombinant Wisp1 protein, and immunohistological analysis of the pancreas of control and treated mice, respectively.

Immunoblot analysis

Islets were lysed in triple detergent lysis buffer (Tris-HCl 50 mM, NaCl 150 mM, 0.1% (w/v) SDS, 1% (v/v) NP40 and 0.5% (w/v) sodium deoxycholate). After 3 consecutive cycles of dry ice and 37 °C, cell debris was pelleted and supernatants were prepared for SDS-PAGE electrophoresis on 8% Tris-tricine homemade gels. Proteins were then transferred to a Polyscreen PVDF membrane (Perkin Elmer, Waltham, MA, USA) and incubated overnight at 4 °C with the antibodies indicated in Supplementary Table 2. Immunoblots were developed with horseradish peroxidase-conjugated secondary antibodies (1:5000, GE Healthcare Bio-Sciences Corp. Piscataway, NJ, USA) and visualized with ECL Reagent (Pierce Biotechnology, Rockford, IL, USA) using a LAS4000 Lumi-Imager (Fuji Photo Film, Valhalla, NY). Protein spots were quantitated with Image J software. Due to the little amount of protein obtained from islets, protein extracts were not quantified but instead, the same number of islets was loaded in each lane. Representative images of the quantification results were selected. Uncropped blots are supplied in the Source Data file.

ELISAS

Mouse Wisp1 levels were determined using a Mouse/Rat Wisp-1/CCN4 Immunoassay (R&D Systems) that detects both natural and full-length recombinant Wisp1 protein. ELISAS to determine serum levels of mouse osteopontin, mouse osteoprogeterin and mouse Igf-1 were purchased from R&D Systems (Abingdon, UK). Mouse insulin was analyzed using an Ultra Sensitive Mouse Insulin ELISA Kit (Crystal Chem, IL, USA). Human WISP1 levels in sera from mice injected with Ad-WISP1 and in archived human plasma samples were determined using a Human WISP1/CCN4 PicoKine^TM ELISA Kit (Boster Biological Technology, California, USA). Specific antibodies for this ELISA were produced using T23-N367 of human WISP1 as immunogen (full-length WISP1 is 367 aminoacids). A total of 11 samples originated from clinically healthy children, aged 2–5 years, and were obtained from the Biobank of the Hospital Infantil Sant Joan de Deu. A total of 14 samples originated from clinically healthy adult men, aged 28–45 years, and were obtained from the Hospital Clinic-IDIBAPS Biobank. Informed consent was obtained for all donors. All assays were performed following the manufacturer´s instructions.

Statistical information

Data were analyzed using GraphPad Prism version 6.00 for Windows (www.graphpad.com) and Microsoft Office Excel 2007, and expressed as the mean ± standard error of the mean (SEM). The appropriate statistical test was determined based on the number of comparisons being done. Student’s t-tests (two-tailed unless otherwise stated) were used for comparison of two groups. One-way ANOVA was used for analysis of three or more experimental groups. Two-way ANOVA was used for analysis of adenoviral WISP1 gene overexpression, mouse serum Wisp1 concentrations and ipGTT tests in in vivo overexpression experiments. When finding significant results in ANOVA, recommended post-hoc tests (Tukey or Sidak) were applied to determine significant differences among multiple comparisons. P < 0.05 was deemed significant. P values greater than 0.05 and lower than 0.1 were considered trends and exact values are shown in the figures.

Ethics statement/study approval

All animal procedures were approved by the Animal Ethics/Research Committee of the University of Barcelona. Principles of laboratory animal care were followed (European and local government guidelines). Experiments involving human islets were performed in agreement with the local ethic committee (CHU, Montpellier) and the institutional ethical committee of the French Agence de la Biomédecine (DC Nos. 2014-2473 and 2016-2716). Informed consent was obtained for all human islet donors. Human blood samples were obtained from the biobanks of the Hospital Infantil Sant Joan de Deu and Hospital Clinic-IDIBAPS. The ethical committees from both hospitals approved the study protocol and sample cession. Informed consent was obtained from all blood donors or from their legal representative.

Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.

Data availability

All data generated or analyzed during this study are included in this published article (and its Supplementary Information files). Source data are provided with this paper.

References

Stewart, A. F. et al. Human beta-cell proliferation and intracellular signaling: part 3. Diabetes 64, 1872–1885 (2015).
Article CAS PubMed PubMed Central Google Scholar
Krishnamurthy, J. et al. p16INK4a induces an age-dependent decline in islet regenerative potential. Nature 443, 453–457 (2006).
Article ADS CAS PubMed Google Scholar
Chen, H. et al. PDGF signalling controls age-dependent proliferation in pancreatic beta-cells. Nature 478, 349–355 (2011).
Article ADS CAS PubMed PubMed Central Google Scholar
Conboy, I. M. et al. Rejuvenation of aged progenitor cells by exposure to a young systemic environment. Nature 433, 760–764 (2005).
Article ADS CAS Google Scholar
Song, G. et al. Use of the parabiotic model in studies of cutaneous wound healing to define the participation of circulating cells. Wound Repair Regen. 18, 426–432 (2010).
Article PubMed PubMed Central Google Scholar
Villeda, S. A. et al. The ageing systemic milieu negatively regulates neurogenesis and cognitive function. Nature 477, 90–94 (2011).
Article ADS CAS PubMed PubMed Central Google Scholar
Salpeter, S. J. et al. Systemic regulation of the age-related decline of pancreatic beta-cell replication. Diabetes 62, 2843–2848 (2013).
Article CAS PubMed PubMed Central Google Scholar
El Ouaamari, A. et al. Liver-derived systemic factors drive beta cell hyperplasia in insulin-resistant states. Cell Rep. 3, 401–410 (2013).
Article PubMed PubMed Central CAS Google Scholar
Stolovich-Rain, M. et al. Weaning triggers a maturation step of pancreatic beta cells. Dev. Cell 32, 535–545 (2015).
Article CAS PubMed Google Scholar
Tsuji, N. et al. Whole organism high content screening identifies stimulators of pancreatic beta-cell proliferation. PLoS ONE 9, e104112 (2014).
Article ADS PubMed PubMed Central CAS Google Scholar
Yi, P., Park, J. S. & Melton, D. A. Betatrophin: a hormone that controls pancreatic beta cell proliferation. Cell 153, 747–758 (2013).
Article CAS PubMed PubMed Central Google Scholar
Bornstein, P. Matricellular proteins: an overview. J. Cell Commun. Signal. 3, 163–165 (2009).
Article PubMed PubMed Central Google Scholar
Yeger, H. & Perbal, B. The CCN family of genes: a perspective on CCN biology and therapeutic potential. J. Cell Commun. Signal. 1, 159–164 (2007).
Article PubMed Google Scholar
Stephens, S. et al. A functional analysis of Wnt inducible signalling pathway protein-1 (WISP-1/CCN4). J. Cell Commun. Signal. 9, 63–72 (2015).
Article MathSciNet PubMed PubMed Central Google Scholar
Holbourn, K. P., Acharya, K. R. & Perbal, B. The CCN family of proteins: structure-function relationships. Trends Biochem. Sci. 33, 461–473 (2008).
Article CAS PubMed PubMed Central Google Scholar
Shi, W. et al. Cyr61 promotes growth of pancreatic carcinoma via nuclear exclusion of p27. Tumour Biol. 35, 11147–11151 (2014).
Article CAS PubMed Google Scholar
Riley, K. G. et al. Connective tissue growth factor modulates adult beta-cell maturity and proliferation to promote beta-cell regeneration in mice. Diabetes 64, 1284–1298 (2015).
Article CAS PubMed Google Scholar
Pennica, D. et al. WISP genes are members of the connective tissue growth factor family that are up-regulated in wnt-1-transformed cells and aberrantly expressed in human colon tumors. Proc. Natl Acad. Sci. USA 95, 14717–14722 (1998).
Article ADS CAS PubMed Google Scholar
Jun, J. I. & Lau, L. F. Taking aim at the extracellular matrix: CCN proteins as emerging therapeutic targets. Nat. Rev. Drug Discov. 10, 945–963 (2011).
Article CAS PubMed PubMed Central Google Scholar
Maiese, K. WISP1: Clinical insights for a proliferative and restorative member of the CCN family. Curr. neurovascular Res. 11, 378–389 (2014).
Article CAS Google Scholar
Maiese, K. Picking a bone with WISP1 (CCN4): new strategies against degenerative joint disease. J. Transl. Sci. 1, 83–85 (2016).
Article PubMed PubMed Central Google Scholar
Maeda, A. et al. WNT1-induced secreted protein-1 (WISP1), a novel regulator of bone turnover and Wnt signaling. J. Biol. Chem. 290, 14004–14018 (2015).
Article CAS PubMed PubMed Central Google Scholar
French, D. M. et al. WISP-1 is an osteoblastic regulator expressed during skeletal development and fracture repair. Am. J. Pathol. 165, 855–867 (2004).
Article CAS PubMed PubMed Central Google Scholar
Macsai, C. E., Georgiou, K. R., Foster, B. K., Zannettino, A. C. & Xian, C. J. Microarray expression analysis of genes and pathways involved in growth plate cartilage injury responses and bony repair. Bone 50, 1081–1091 (2012).
Article CAS PubMed Google Scholar
Murahovschi, V. et al. WISP1 is a novel adipokine linked to inflammation in obesity. Diabetes 64, 856–866 (2015).
Article CAS PubMed Google Scholar
Ferrand, N. et al. WISP1/CCN4 inhibits adipocyte differentiation through repression of PPARgamma activity. Sci. Rep. 7, 1749 (2017).
Article ADS PubMed PubMed Central CAS Google Scholar
Horbelt, T. et al. The novel adipokine WISP1 associates with insulin resistance and impairs insulin action in human myotubes and mouse hepatocytes. Diabetologia 61, 2054–2065 (2018).
Article PubMed CAS Google Scholar
Barchetta, I. et al. WISP1 is a marker of systemic and adipose tissue inflammation in dysmetabolic subjects with or without type 2 diabetes. J. Endocr. Soc. 1, 660–670 (2017).
Burke, S. J. et al. Regulation of the CCL2 gene in pancreatic beta-cells by IL-1beta and glucocorticoids: role of MKP-1. PLoS ONE 7, e46986 (2012).
Article ADS CAS PubMed PubMed Central Google Scholar
Otonkoski, T., Knip, M., Wong, I. & Simell, O. Effects of growth hormone and insulin-like growth factor I on endocrine function of human fetal islet-like cell clusters during long-term tissue culture. Diabetes 37, 1678–1683 (1988).
Article CAS PubMed Google Scholar
Kulkarni, R. N. et al. beta-cell-specific deletion of the Igf1 receptor leads to hyperinsulinemia and glucose intolerance but does not alter beta-cell mass. Nat. Genet. 31, 111–115 (2002).
Article CAS PubMed Google Scholar
Lyssenko, V. et al. Pleiotropic effects of GIP on islet function involve osteopontin. Diabetes 60, 2424–2433 (2011).
Article CAS PubMed PubMed Central Google Scholar
Arafat, H. A. et al. Osteopontin protects the islets and beta-cells from interleukin-1 beta-mediated cytotoxicity through negative feedback regulation of nitric oxide. Endocrinology 148, 575–584 (2007).
Article CAS PubMed Google Scholar
Kondegowda, N. G. et al. Osteoprotegerin and denosumab stimulate human beta cell proliferation through inhibition of the receptor activator of NF-kappaB ligand pathway. Cell Metab. 22, 77–85 (2015).
Article CAS PubMed PubMed Central Google Scholar
Piemonti, L. et al. Human pancreatic islets produce and secrete MCP-1/CCL2: relevance in human islet transplantation. Diabetes 51, 55–65 (2002).
Article CAS PubMed Google Scholar
Bonner-Weir, S., Aguayo-Mazzucato, C. & Weir, G. C. Dynamic development of the pancreas from birth to adulthood. Upsala J. Med. Sci. 121, 155–158 (2016).
Article PubMed Google Scholar
Wang, Y. et al. Dual effect of raptor on neonatal beta-cell proliferation and identity maintenance. Diabetes 68, 1950–1964 (2019).
Article CAS PubMed Google Scholar
Wang, P. et al. A high-throughput chemical screen reveals that harmine-mediated inhibition of DYRK1A increases human pancreatic beta cell replication. Nat. Med. 21, 383–388 (2015).
Article CAS PubMed PubMed Central Google Scholar
Levasseur, E. M. et al. Hypusine biosynthesis in beta cells links polyamine metabolism to facultative cellular proliferation to maintain glucose homeostasis. Sci. Signal. 12, eaax0715 (2019).
Article CAS PubMed PubMed Central Google Scholar
Wang, P. et al. Diabetes mellitus-advances and challenges in human beta-cell proliferation. Nat. Rev. Endocrinol. 11, 201–212 (2015).
Article CAS Google Scholar
Lu, S. et al. WISP1 overexpression promotes proliferation and migration of human vascular smooth muscle cells via AKT signaling pathway. Eur. J. Pharmacol. 788, 90–97 (2016).
Article CAS PubMed Google Scholar
Su, F., Overholtzer, M., Besser, D. & Levine, A. J. WISP-1 attenuates p53-mediated apoptosis in response to DNA damage through activation of the Akt kinase. Genes Dev. 16, 46–57 (2002).
Article CAS PubMed PubMed Central Google Scholar
Sinha, M. et al. Restoring systemic GDF11 levels reverses age-related dysfunction in mouse skeletal muscle. Science 344, 649–652 (2014).
Article ADS CAS PubMed PubMed Central Google Scholar
Loffredo, F. S. et al. Growth differentiation factor 11 is a circulating factor that reverses age-related cardiac hypertrophy. Cell 153, 828–839 (2013).
Article CAS PubMed PubMed Central Google Scholar
Katsimpardi, L. et al. Vascular and neurogenic rejuvenation of the aging mouse brain by young systemic factors. Science 344, 630–634 (2014).
Article ADS CAS PubMed PubMed Central Google Scholar
Clement-Lacroix, P. et al. Osteoblasts are a new target for prolactin: analysis of bone formation in prolactin receptor knockout mice. Endocrinology 140, 96–105 (1999).
Article CAS PubMed Google Scholar
Guntur, A. R. & Rosen, C. J. Bone as an endocrine organ. Endocr. Pract. 18, 758–762 (2012).
Article PubMed PubMed Central Google Scholar
Shao, J. et al. Bone regulates glucose metabolism as an endocrine organ through osteocalcin. Int. J. Endocrinol. 2015, 967673 (2015).
Article PubMed PubMed Central CAS Google Scholar
Wei, J., Hanna, T., Suda, N., Karsenty, G. & Ducy, P. Osteocalcin promotes beta-cell proliferation during development and adulthood through Gprc6a. Diabetes 63, 1021–1031 (2014).
Article CAS PubMed PubMed Central Google Scholar
Tacke, C. et al. Assessment of circulating Wnt1 inducible signalling pathway protein 1 (WISP-1)/CCN4 as a novel biomarker of obesity. J. Cell Commun. Signal. 12, 539–548 (2018).
Article PubMed Google Scholar
Stamateris, R. E., Sharma, R. B., Hollern, D. A. & Alonso, L. C. Adaptive beta-cell proliferation increases early in high-fat feeding in mice, concurrent with metabolic changes, with induction of islet cyclin D2 expression. Am. J. Physiol. Endocrinol. Metab. 305, E149–E159 (2013).
Article CAS PubMed PubMed Central Google Scholar
Klee, S., Lehmann, M., Wagner, D. E., Baarsma, H. A. & Konigshoff, M. WISP1 mediates IL-6-dependent proliferation in primary human lung fibroblasts. Sci. Rep. 6, 20547 (2016).
Article ADS CAS PubMed PubMed Central Google Scholar
Ono, M. et al. CCN4/WISP1 controls cutaneous wound healing by modulating proliferation, migration and ECM expression in dermal fibroblasts via alpha5beta1 and TNFalpha. Matrix Biol. 68-69, 533–546 (2018).
Article CAS PubMed PubMed Central Google Scholar
Zhang, X. et al. Knockdown of WISP1 inhibit proliferation and induce apoptosis in ALL Jurkat cells. Int. J. Clin. Exp. Pathol. 8, 15489–15496 (2015).
CAS PubMed PubMed Central Google Scholar
Lau, L. F. Cell surface receptors for CCN proteins. J. Cell Commun. Signal. 10, 121–127 (2016).
Article PubMed PubMed Central Google Scholar
Maiese, K., Chong, Z. Z., Shang, Y. C. & Wang, S. Targeting disease through novel pathways of apoptosis and autophagy. Expert Opin. Ther. Targets 16, 1203–1214 (2012).
Article CAS PubMed PubMed Central Google Scholar
Bernal-Mizrachi, E., Wen, W., Stahlhut, S., Welling, C. M. & Permutt, M. A. Islet beta cell expression of constitutively active Akt1/PKB alpha induces striking hypertrophy, hyperplasia, and hyperinsulinemia. J. Clin. Invest. 108, 1631–1638 (2001).
Article CAS PubMed PubMed Central Google Scholar
Tuttle, R. L. et al. Regulation of pancreatic beta-cell growth and survival by the serine/threonine protein kinase Akt1/PKBalpha. Nat. Med. 7, 1133–1137 (2001).
Article CAS PubMed Google Scholar
Hennige, A. M. et al. Upregulation of insulin receptor substrate-2 in pancreatic beta cells prevents diabetes. J. Clin. Investig. 112, 1521–1532 (2003).
Article CAS PubMed Google Scholar
Withers, D. J. et al. Irs-2 coordinates Igf-1 receptor-mediated beta-cell development and peripheral insulin signalling. Nat. Genet. 23, 32–40 (1999).
Article CAS PubMed Google Scholar
Withers, D. J. et al. Disruption of IRS-2 causes type 2 diabetes in mice. Nature 391, 900–904 (1998).
Article ADS CAS PubMed Google Scholar
Pardo, F. N. et al. The role of Raf-1 kinase inhibitor protein in the regulation of pancreatic beta cell proliferation in mice. Diabetologia 55, 3331–3340 (2012).
Article CAS PubMed Google Scholar
Broca, C. et al. Proteasome dysfunction mediates high glucose-induced apoptosis in rodent beta cells and human islets. PLoS ONE 9, e92066 (2014).
Article ADS PubMed PubMed Central Google Scholar
Figueiredo, H. et al. Targeting pancreatic islet PTP1B improves islet graft revascularization and transplant outcomes. Sci. Transl. Med. 11, eaar6294 (2019).
Article PubMed CAS Google Scholar
Ono, M., Inkson, C. A., Kilts, T. M. & Young, M. F. WISP-1/CCN4 regulates osteogenesis by enhancing BMP-2 activity. J. Bone Miner. Res. 26, 193–208 (2011).
Article CAS PubMed Google Scholar
Gasa, R. et al. Proendocrine genes coordinate the pancreatic islet differentiation program in vitro. Proc. Natl Acad. Sci. USA 101, 13245–13250 (2004).
Article ADS CAS PubMed Google Scholar
Ejarque, M. et al. Neurogenin3 cooperates with Foxa2 to autoactivate its own expression. J. Biol. Chem. 288, 11705–11717 (2013).
Article CAS PubMed PubMed Central Google Scholar

Download references

Acknowledgements

We are indebted to the IDIBAPS Biobank and to the Hospital Infantil Sant Joan de Deu per a la investigació Biobank, both integrated in the Spanish National Biobank Network of ISCIII, for the sample and data procurement. This work has been supported by projects PI13/01500, PI16/00774 (to R.Ga. and R.Go.) and PI19/00896 (to R.Ga.) integrated in the Plan Estatal de I+D+I and cofinanced by ISCIII-Subdirección General de Evaluación and Fondo Europeo de Desarrollo Regional (FEDER-A way to build Europe); grant 2014 SGR659 (to R.Go.) from the Generalitat de Catalunya; VIII Ayuda SED a Proyectos de Investigación Básica en Diabetes dirigidos por Jóvenes Investigadores (to R.F.R.) from the Sociedad Española de Diabetes Foundation and by the Cátedra Astra-Zeneca (to R.Go.). This work was supported in part by the Intramural Research Program of the NIDCR, NIH (to M.F.Y.). M.F. has been funded by Fundación DiabetesCERO. CIBERDEM (Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas) is an initiative of the Instituto de Salud Carlos III.

Author information

Authors and Affiliations

August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Rosselló 149-153, 08036, Barcelona, Spain
Rebeca Fernandez-Ruiz, Ainhoa García-Alamán, Yaiza Esteban, Joan Mir-Coll, Berta Serra-Navarro, Marta Fontcuberta-PiSunyer, Josep Vidal, Ramon Gomis & Rosa Gasa
Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Barcelona, Spain
Rebeca Fernandez-Ruiz, Ainhoa García-Alamán, Yaiza Esteban, Josep Vidal, Ramon Gomis & Rosa Gasa
University of Barcelona, Barcelona, Spain
Rebeca Fernandez-Ruiz, Joan Mir-Coll, Berta Serra-Navarro & Ramon Gomis
CHU Montpellier, Laboratory of Cell Therapy for Diabetes (LTCD), Hospital St-Eloi, Montpellier, France
Christophe Broca, Mathieu Armanet & Anne Wojtusciszyn
Service of Endocrinology, Diabetes and Metabolism, Lausanne University Hospital, Lausanne, Switzerland
Anne Wojtusciszyn
Molecular Biology of Bones and Teeth Section, NIDCR, National Institutes of Health, Bethesda, MD, USA
Vardit Kram & Marian F. Young
Department of Endocrinology and Nutrition, Hospital Clinic of Barcelona, Barcelona, Spain
Josep Vidal
Universitat Oberta de Catalunya (UOC), Barcelona, Spain
Ramon Gomis

Authors

Rebeca Fernandez-Ruiz
View author publications
You can also search for this author in PubMed Google Scholar
Ainhoa García-Alamán
View author publications
You can also search for this author in PubMed Google Scholar
Yaiza Esteban
View author publications
You can also search for this author in PubMed Google Scholar
Joan Mir-Coll
View author publications
You can also search for this author in PubMed Google Scholar
Berta Serra-Navarro
View author publications
You can also search for this author in PubMed Google Scholar
Marta Fontcuberta-PiSunyer
View author publications
You can also search for this author in PubMed Google Scholar
Christophe Broca
View author publications
You can also search for this author in PubMed Google Scholar
Mathieu Armanet
View author publications
You can also search for this author in PubMed Google Scholar
Anne Wojtusciszyn
View author publications
You can also search for this author in PubMed Google Scholar
Vardit Kram
View author publications
You can also search for this author in PubMed Google Scholar
Marian F. Young
View author publications
You can also search for this author in PubMed Google Scholar
Josep Vidal
View author publications
You can also search for this author in PubMed Google Scholar
Ramon Gomis
View author publications
You can also search for this author in PubMed Google Scholar
Rosa Gasa
View author publications
You can also search for this author in PubMed Google Scholar

Contributions

R.F.R. conducted all experiments. A.G. provided assistance with mouse experiments and immunohistochemistry assays. Y.E., J.M., B.S., and M.F. provided assistance in several experiments. C.B., M.A., and A.W. performed isolation of human islets. M.F.Y. and V.K. provided reagents and performed experiments in bone. R.F.R. and R.Ga. conceived the project. R.F.R., J.V., R.Go., and R.Ga. analyzed and discussed the data. R.F.R. and R.Ga. wrote the paper.

Corresponding author

Correspondence to Rosa Gasa.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Peer review information Nature Communications thanks the anonymous reviewers for their contribution to the peer review of this work. Peer reviewer reports are available.

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Supplementary Information

Peer Review File

Description of Additional Supplementary Files

Supplementary Movie 1

Supplementary Movie 2

Supplementary Movie 3

Supplementary Movie 4

Supplementary Movie 5

Supplementary Movie 6

Supplementary Movie 7

Supplementary Movie 8

Supplementary Movie 9

Supplementary Movie 10

Reporting Summary

Source data

Source Data

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and permissions

About this article

Cite this article

Fernandez-Ruiz, R., García-Alamán, A., Esteban, Y. et al. Wisp1 is a circulating factor that stimulates proliferation of adult mouse and human beta cells. Nat Commun 11, 5982 (2020). https://doi.org/10.1038/s41467-020-19657-1

Download citation

Received: 13 February 2019
Accepted: 16 October 2020
Published: 25 November 2020
DOI: https://doi.org/10.1038/s41467-020-19657-1

This article is cited by

ISL1 controls pancreatic alpha cell fate and beta cell maturation
- Romana Bohuslavova
- Valeria Fabriciova
- Gabriela Pavlinkova
Cell & Bioscience (2023)
CCN proteins: opportunities for clinical studies—a personal perspective
- Herman Yeger
Journal of Cell Communication and Signaling (2023)
Recent progress on the role of cellular communication network factors (CCN) 3, 4 and 6 in regulating adiposity, liver fibrosis and pancreatic islets
- Viktoria Xega
- Tara Alami
- Jun-Li Liu
Journal of Cell Communication and Signaling (2023)

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.