Skip to main content

Advertisement

Log in

Progranulin expression is upregulated after spinal contusion in mice

  • Original Paper
  • Published:
Acta Neuropathologica Aims and scope Submit manuscript

Abstract

Progranulin (proepithelin) is a pleiotropic growth-factor associated with inflammation and wound repair in peripheral tissues. It also has been implicated in the response to acute traumatic brain injury as well as to chronic neurodegenerative diseases. To determine whether changes in progranulin expression also accompany acute spinal cord injury, C57BL/6 mice were subjected to mid-thoracic (T9 level) contusion spinal cord injury and analyzed by immunohistochemical and biochemical methods. Whereas spinal cord sections prepared from non-injured laminectomy control animals contained low basal levels of progranulin immunoreactivity in gray matter, sections from injured animals contained intense immunoreactivity throughout the injury epicenter that peaked 7–14 days post injury. Progranulin immunoreactivity colocalized with myeloid cell markers CD11b and CD68, indicating that expression increased primarily in activated microglia and macrophages. Immunoblot analysis confirmed that progranulin protein levels rose after injury. On the basis of quantitative polymerase chain reaction analysis, increased protein levels resulted from a tenfold rise in progranulin transcripts. These data demonstrate that progranulin is dramatically induced in myeloid cells after experimental spinal cord injury and is positioned appropriately both spatially and temporally to influence recovery after injury.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  1. Ahmed Z, Mackenzie IR, Hutton ML, Dickson DW (2007) Progranulin in frontotemporal lobar degeneration and neuroinflammation. J Neuroinflamm 4:7

    Article  CAS  Google Scholar 

  2. Baba T, Hoff HB III, Nemoto H et al (1993) Acrogranin, an acrosomal cysteine-rich glycoprotein, is the precursor of the growth-modulating peptides, granulins, and epithelins, and is expressed in somatic as well as male germ cells. Mol Reprod Dev 34:233–243

    Article  CAS  PubMed  Google Scholar 

  3. Baker CA, Manuelidis L (2003) Unique inflammatory RNA profiles of microglia in Creutzfeldt-Jakob disease. Proc Natl Acad Sci USA 100:675–679

    Article  CAS  PubMed  Google Scholar 

  4. Baker M, Mackenzie IR, Pickering-Brown SM et al (2006) Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 442:916–919

    Article  CAS  PubMed  Google Scholar 

  5. Bhandari V, Daniel R, Lim PS, Bateman A (1996) Structural and functional analysis of a promoter of the human granulin/epithelin gene. Biochem J 319:441–447

    CAS  PubMed  Google Scholar 

  6. Bhandari V, Palfree RG, Bateman A (1992) Isolation and sequence of the granulin precursor cDNA from human bone marrow reveals tandem cysteine-rich granulin domains. Proc Natl Acad Sci USA 89:1715–1719

    Article  CAS  PubMed  Google Scholar 

  7. Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254

    Article  CAS  PubMed  Google Scholar 

  8. Brouwers N, Sleegers K, Engelborghs S et al (2008) Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease. Neurology 71:656–664

    Article  CAS  PubMed  Google Scholar 

  9. Carmel JB, Kakinohana O, Mestril R, Young W, Marsala M, Hart RP (2004) Mediators of ischemic preconditioning identified by microarray analysis of rat spinal cord. Exp Neurol 185:81–96

    Article  CAS  PubMed  Google Scholar 

  10. Chen-Plotkin AS, Xiao J, Geser F et al. (2009) Brain progranulin expression in GRN-associated frontotemporal lobar degeneration. Acta Neuropathol (in press). doi:10.1007/s00401-009-0576-2

  11. Cruts M, Gijselinck I, van der Zee J et al (2006) Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 442:920–924

    Article  CAS  PubMed  Google Scholar 

  12. Daniel R, Daniels E, He Z, Bateman A (2003) Progranulin (acrogranin/PC cell-derived growth factor/granulin-epithelin precursor) is expressed in the placenta, epidermis, microvasculature, and brain during murine development. Dev Dyn 227:593–599

    Article  CAS  PubMed  Google Scholar 

  13. Daniel R, He Z, Carmichael KP, Halper J, Bateman A (2000) Cellular localization of gene expression for progranulin. J Histochem Cytochem 48:999–1009

    CAS  PubMed  Google Scholar 

  14. Donnelly DJ, Gensel JC, Ankeny DP, van Rooijen N, Popovich PG (2009) An efficient and reproducible method for quantifying macrophages in different experimental models of central nervous system pathology. J Neurosci Meth 181:36–44

    Article  CAS  Google Scholar 

  15. Donnelly DJ, Popovich PG (2008) Inflammation and its role in neuroprotection, axonal regeneration and functional recovery after spinal cord injury. Exp Neurol 209:378–388

    Article  CAS  PubMed  Google Scholar 

  16. Fitch MT, Silver J (2008) CNS injury, glial scars, and inflammation: Inhibitory extracellular matrices and regeneration failure. Exp Neurol 209:294–301

    Article  CAS  PubMed  Google Scholar 

  17. Hanington PC, Barreda DR, Belosevic M (2006) A novel hematopoietic granulin induces proliferation of goldfish (Carassius auratus L.) macrophages. J Biol Chem 281:9963–9970

    Article  CAS  PubMed  Google Scholar 

  18. He Z, Bateman A (2003) Progranulin (granulin-epithelin precursor, PC-cell-derived growth factor, acrogranin) mediates tissue repair and tumorigenesis. J Mol Med 81:600–612

    Article  CAS  PubMed  Google Scholar 

  19. He Z, Ong CH, Halper J, Bateman A (2003) Progranulin is a mediator of the wound response. Nat Med 9:225–229

    Article  CAS  PubMed  Google Scholar 

  20. Holness CL, da Silva RP, Fawcett J, Gordon S, Simmons DL (1993) Macrosialin, a mouse macrophage-restricted glycoprotein, is a member of the lamp/lgp family. J Biol Chem 268:9661–9666

    CAS  PubMed  Google Scholar 

  21. Holness CL, Simmons DL (1993) Molecular cloning of CD68, a human macrophage marker related to lysosomal glycoproteins. Blood 81:1607–1613

    CAS  PubMed  Google Scholar 

  22. Hrabal R, Chen Z, James S, Bennett HP, Ni F (1996) The hairpin stack fold, a novel protein architecture for a new family of protein growth factors. Nat Struct Biol 3:747–752

    Article  CAS  PubMed  Google Scholar 

  23. Jakeman LB, Guan Z, Wei P et al (2000) Traumatic spinal cord injury produced by controlled contusion in mouse. J Neurotrauma 17:299–319

    Article  CAS  PubMed  Google Scholar 

  24. Jones TB, Basso DM, Sodhi A et al (2002) Pathological CNS autoimmune disease triggered by traumatic spinal cord injury: implications for autoimmune vaccine therapy. J Neurosci 22:2690–2700

    CAS  PubMed  Google Scholar 

  25. Kessenbrock K, Frohlich L, Sixt M et al (2008) Proteinase 3 and neutrophil elastase enhance inflammation in mice by inactivating antiinflammatory progranulin. J Clin Invest 118:2438–2447

    CAS  PubMed  Google Scholar 

  26. Kigerl KA, Lai W, Rivest S, Hart RP, Satoskar AR, Popovich PG (2007) Toll-like receptor (TLR)-2 and TLR-4 regulate inflammation, gliosis, and myelin sparing after spinal cord injury. J Neurochem 102:37–50

    Article  CAS  PubMed  Google Scholar 

  27. Kigerl KA, McGaughy VM, Popovich PG (2006) Comparative analysis of lesion development and intraspinal inflammation in four strains of mice following spinal contusion injury. J Comp Neurol 494:578–594

    Article  PubMed  CAS  Google Scholar 

  28. Kojima Y, Ono K, Inoue K et al (2009) Progranulin expression in advanced human atherosclerotic plaque. Atherosclerosis 206:102–108

    Article  CAS  PubMed  Google Scholar 

  29. Kramps JA, van Twisk C, van der Linden AC (1983) l-Pyroglutamyl-l-prolyl-l-valine-p-nitroanilide, a highly specific substrate for granulocyte elastase. Scand J Clin Lab Invest 43:427–432

    Article  CAS  PubMed  Google Scholar 

  30. Kurushima H, Ramprasad M, Kondratenko N, Foster DM, Quehenberger O, Steinberg D (2000) Surface expression and rapid internalization of macrosialin (mouse CD68) on elicited mouse peritoneal macrophages. J Leukoc Biol 67:104–108

    CAS  PubMed  Google Scholar 

  31. Lee MK, Tuttle JB, Rebhun LI, Cleveland DW, Frankfurter A (1990) The expression and posttranslational modification of a neuron-specific beta-tubulin isotype during chick embryogenesis. Cell Motil Cytoskeleton 17:118–132

    Article  CAS  PubMed  Google Scholar 

  32. Li G, Yin H, Kuret J (2004) Casein kinase 1 delta phosphorylates tau and disrupts its binding to microtubules. J Biol Chem 279:15938–15945

    Article  CAS  PubMed  Google Scholar 

  33. Li X, Massa PE, Hanidu A et al (2002) IKKalpha, IKKbeta, and NEMO/IKKgamma are each required for the NF-kappa B-mediated inflammatory response program. J Biol Chem 277:45129–45140

    Article  CAS  PubMed  Google Scholar 

  34. Liu NK, Xu XM (2006) β-Tubulin is a more suitable internal control than β-actin in western blot analysis of spinal cord tissues after traumatic injury. J Neurotrauma 23:1794–1801

    Article  PubMed  Google Scholar 

  35. Ma M, Basso DM, Walters P, Stokes BT, Jakeman LB (2001) Behavioral and histological outcomes following graded spinal cord contusion injury in the C57Bl/6 mouse. Exp Neurol 169:239–254

    Article  CAS  PubMed  Google Scholar 

  36. Mackenzie IR, Baker M, Pickering-Brown S et al (2006) The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene. Brain 129:3081–3090

    Article  PubMed  Google Scholar 

  37. Malaspina A, Kaushik N, de Belleroche J (2001) Differential expression of 14 genes in amyotrophic lateral sclerosis spinal cord detected using gridded cDNA arrays. J Neurochem 77:132–145

    Article  CAS  PubMed  Google Scholar 

  38. Matzilevich DA, Rall JM, Moore AN, Grill RJ, Dash PK (2002) High-density microarray analysis of hippocampal gene expression following experimental brain injury. J Neurosci Res 67:646–663

    Article  CAS  PubMed  Google Scholar 

  39. Moisse K, Volkening K, Leystra-Lantz C, Welch I, Hill T, Strong MJ (2009) Divergent patterns of cytosolic TDP-43 and neuronal progranulin expression following axotomy: implications for TDP-43 in the physiological response to neuronal injury. Brain Res 1249:202–211

    Article  CAS  PubMed  Google Scholar 

  40. Mukherjee O, Pastor P, Cairns NJ et al (2006) HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin. Ann Neurol 60:314–322

    Article  CAS  PubMed  Google Scholar 

  41. Ohmi K, Greenberg DS, Rajavel KS, Ryazantsev S, Li HH, Neufeld EF (2003) Activated microglia in cortex of mouse models of mucopolysaccharidoses I and IIIB. Proc Natl Acad Sci USA 100:1902–1907

    Article  CAS  PubMed  Google Scholar 

  42. Pereson S, Wils H, Kleinberger G et al (2009) Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models. J Pathol 219:173–181

    Article  CAS  PubMed  Google Scholar 

  43. Plowman GD, Green JM, Neubauer MG et al (1992) The epithelin precursor encodes two proteins with opposing activities on epithelial cell growth. J Biol Chem 267:13073–13078

    CAS  PubMed  Google Scholar 

  44. Popovich PG, Hickey WF (2001) Bone marrow chimeric rats reveal the unique distribution of resident and recruited macrophages in the contused rat spinal cord. J Neuropathol Exp Neurol 60:676–685

    CAS  PubMed  Google Scholar 

  45. Popovich PG, Wei P, Stokes BT (1997) Cellular inflammatory response after spinal cord injury in Sprague-Dawley and Lewis rats. J Comp Neurol 377:443–464

    Article  CAS  PubMed  Google Scholar 

  46. Qin J, Diaz-Cueto L, Schwarze JE et al (2005) Effects of progranulin on blastocyst hatching and subsequent adhesion and outgrowth in the mouse. Biol Reprod 73:434–442

    Article  CAS  PubMed  Google Scholar 

  47. Ririe KM, Rasmussen RP, Wittwer CT (1997) Product differentiation by analysis of DNA melting curves during the polymerase chain reaction. Anal Biochem 245:154–160

    Article  CAS  PubMed  Google Scholar 

  48. Schmittgen TD, Livak KJ (2008) Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc 3:1101–1108

    Article  CAS  PubMed  Google Scholar 

  49. Schnell L, Fearn S, Klassen H, Schwab ME, Perry VH (1999) Acute inflammatory responses to mechanical lesions in the CNS: differences between brain and spinal cord. Eur J Neurosci 11:3648–3658

    Article  CAS  PubMed  Google Scholar 

  50. Schroeder A, Mueller O, Stocker S et al (2006) The RIN: an RNA integrity number for assigning integrity values to RNA measurements. BMC Mol Biol 7:3

    Article  PubMed  CAS  Google Scholar 

  51. Shankaran SS, Capell A, Hruscha AT et al (2008) Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion. J Biol Chem 283:1744–1753

    Article  CAS  PubMed  Google Scholar 

  52. Sleegers K, Brouwers N, Maurer-Stroh S et al (2008) Progranulin genetic variability contributes to amyotrophic lateral sclerosis. Neurology 71:253–259

    Article  CAS  PubMed  Google Scholar 

  53. Solovjov DA, Pluskota E, Plow EF (2005) Distinct roles for the alpha and beta subunits in the functions of integrin alphaMbeta2. J Biol Chem 280:1336–1345

    Article  CAS  PubMed  Google Scholar 

  54. Sparro G, Galdenzi G, Eleuteri AM, Angeletti M, Schroeder W, Fioretti E (1997) Isolation and N-terminal sequence of multiple forms of granulins in human urine. Protein Expr Purif 10:169–174

    Article  CAS  PubMed  Google Scholar 

  55. Sroga JM, Jones TB, Kigerl KA, McGaughy VM, Popovich PG (2003) Rats and mice exhibit distinct inflammatory reactions after spinal cord injury. J Comp Neurol 462:223–240

    Article  PubMed  Google Scholar 

  56. Tonai T, Shiba K, Taketani Y et al (2001) A neutrophil elastase inhibitor (ONO-5046) reduces neurologic damage after spinal cord injury in rats. J Neurochem 78:1064–1072

    Article  CAS  PubMed  Google Scholar 

  57. Van Damme P, Van Hoecke A, Lambrechts D et al (2008) Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival. J Cell Biol 181:37–41

    Article  PubMed  CAS  Google Scholar 

  58. van der Zee J, Le Ber I, Maurer-Stroh S et al (2007) Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia. Hum Mutat 28:416

    PubMed  Google Scholar 

  59. Youn BS, Bang SI, Kloting N et al (2009) Serum progranulin concentrations may be associated with macrophage infiltration into omental adipose tissue. Diabetes 58:627–636

    Article  CAS  PubMed  Google Scholar 

  60. Young W (2002) Spinal cord contusion models. Prog Brain Res 137:231–255

    Article  PubMed  Google Scholar 

  61. Zhou J, Gao G, Crabb JW, Serrero G (1993) Purification of an autocrine growth factor homologous with mouse epithelin precursor from a highly tumorigenic cell line. J Biol Chem 268:10863–10869

    CAS  PubMed  Google Scholar 

  62. Zhu J, Nathan C, Jin W et al (2002) Conversion of proepithelin to epithelins: roles of SLPI and elastase in host defense and wound repair. Cell 111:867–878

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

We thank Dr. Mariano Viapiano (Department of Neurosurgery) for guidance with imaging methods. This work was supported by The Ohio State University Neuroscience Signature Program (S.K.K., L.B.J., J.K.), National Institute for Neurological Disorders and Stroke (P.G.P.), Neuroscience Core Center (NS045758), and The Ohio State Center for Brain and Spinal Cord Repair.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jeff Kuret.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Naphade, S.B., Kigerl, K.A., Jakeman, L.B. et al. Progranulin expression is upregulated after spinal contusion in mice. Acta Neuropathol 119, 123–133 (2010). https://doi.org/10.1007/s00401-009-0616-y

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00401-009-0616-y

Keywords

Navigation