Data supporting the effects of xanthine derivative KMUP-3 on vascular smooth muscle cell calcification and abdominal aortic aneurysm in mice

No pharmacotherapy in the clinical setting has been available to alter the natural history of abdominal aortic aneurysm (AAA). Targeting vascular smooth muscle cell (VSMC) dysfunction during the pathogenesis of AAA, including phenotypic switch and apoptosis, could be a potential strategy to limit AAA growth. Here, we provide additional information regarding materials, methods and data related to our recent study published in Atherosclerosis [1]. The therapeutic potential of a self-developed xanthine derivative KMUP-3 was evaluated in VSMC calcification and abdominal aortic aneurysm (AAA). In vitro VSMC calcification was induced using β-glycerophosphate, and AAA was induced using angiotensin II infusion for 4 weeks in apolipoprotein E-deficient mice. The data contained in this article support the effects of KMUP-3 on VSMC calcification and AAA.

No pharmacotherapy in the clinical setting has been available to alter the natural history of abdominal aortic aneurysm (AAA). Targeting vascular smooth muscle cell (VSMC) dysfunction during the pathogenesis of AAA, including phenotypic switch and apoptosis, could be a potential strategy to limit AAA growth. Here, we provide additional information regarding materials, methods and data related to our recent study published in Atherosclerosis [1] . The therapeutic potential of a self-developed xanthine derivative KMUP-3 was evaluated in VSMC calcification and abdominal aor-tic aneurysm (AAA). In vitro VSMC calcification was induced using β-glycerophosphate, and AAA was induced using angiotensin II infusion for 4 weeks in apolipoprotein E-deficient mice. The data contained in this article support the effects of KMUP-3 on VSMC calcification and AAA.
© 2020 The Author(s

Value of the data
• The data provides evidence supporting vascular smooth muscle cell dysfunction as a target for treating abdominal aortic aneurysm. • The data may be used by vascular biologists and other scientists exploring the pathogenesis of vascular calcification and abdominal aortic aneurysm. • The data may be useful for further investigations regarding vascular calcification, abdominal aortic aneurysm and other vascular diseases.

Data description
The data demonstrates the inhibitory effects of a xanthine derivative 7- Fig. 1 ) in vascular calcification and abdominal aortic aneurysm (AAA), serving as supporting data for our recent study [1] .
We have demonstrated that KMUP-3 inhibits angiotensin II (AngII)-infused AAA [1] . Therefore, we investigated phosphorylated mTOR (p-mTOR) and phosphorylated AMP-activated protein kinase (p-AMPK) expression in the AAA specimens. On day 14, treatment with KMUP-3 led to reduced p-mTOR expression ( Fig. 3 A and B) and increased p-AMPK expression ( Fig. 3 C & D) in the medial layer, compatible with what we have observed In vitro [1] . As shown by quantitative real-time polymerase chain reaction (qRT-PCR), the aortic expression of miR-29b, a microRNA regulating apoptosis during aneurysm formation [3] , was lower in the AngII-KMUP-3 group than in the AngII group ( Fig. 4 A). Also, KMUP-3 treatment increased the Bcl-2/Bax ratio ( Fig. 4 B), compatible with the In vitro findings ( Fig. 2 C).
Finally, whether vascular calcification can be altered KMUP-3 treatment was investigated. Compared with the AngII group, aortic valve calcification ( Fig. 5 A) and medial calcification in the aortic wall ( Fig. 5 B) in the AngII-KMUP-3 group were attenuated. Consistently, the alkaline phosphatase (ALP) activity in the aortic wall was increased in the AngII group, and the activity was lowered in the AngII-KMUP-3 group ( Fig. 5 C).

Primary rat VSMC culture and In vitro VSMC calcification
The experimental details of In vitro VSMC calcification are described in our recent study [1] .

Alizarin red S staining and calcium content in VSMC culture
Calcium deposition was analyzed using alizarin red S staining (Sigma-Aldrich, St. Louis, MO). After fixation with 75% ethanol, cells were stained with 2% alizarin red S solution for 1 h at 37 °C. The cells were incubated in 10% cetylpyridinium chloride solution (Sigma-Aldrich) for 30 min. The absorbance of the released alizarin red was measured at 540 nm. The calcium content in the cell lysates was evaluated using a QuantiChrom Calcium Assay kit (BioAssay Systems, Hayward, CA). The absorbance was measured at 612 nm using an automated microplate reader (Spectra-Max 340PC384; Molecular Devices, Sunnyvale, CA).

ALP activity
To evaluate the activity of ALP in the cell culture, VSMCs were washed and lysed in Mammalian Protein Extraction Reagent (M-PER; Pierce, Rockford, IL). Samples were incubated in 0.1 M NaHCO3/Na2CO3 buffer containing 0.1% Triton X-100, 2 mM MgSO4 and 6 mM 4-nitrophenyl phosphate for 1 h at room temperature. The reaction was terminated by addition of 1 M NaOH.  To evaluate the activity of ALP in aortic homogenates, the alkaline phosphatase activity colorimetric assay kit (BioVision, Milpitas, CA) was used based on the manufacturer's instructions. The ALP activity was determined by the absorbance at 405 nm.

Cell viability assay
The MTT assay (Sigma-Aldrich) was performed to assess VSMC viability. In brief, MTT (0.5 mg/ml) was added into the medium for 1 h. The culture medium was removed. Subsequently, the cells were dissolved in isopropanol and shaken for 15 min. The amount of MTT formazan product was quantified using an ELISA reader (Dynex Technologies, Berlin, Germany) at absorbances of 540 nm and 630 nm.

AngII-infused AAA model and KMUP-3 treatment
Treatment of KMUP-3 in the AngII-infused AAA model and other experimental details, including histological analysis, qRT-PCR and western blot analysis, are described in our recent study [1] . The whole study was approved by Institutional Animal Care and Use Committee of Kaohsiung Medical University (Number: 104,231) and conformed to the Guide for the Care and Use of Laboratory Animals published by the National Institutes of Health (NIH Publication #85-23, revised 1996).

Statistics analysis
Statistical analyses were performed using Prism 6 (GraphPad Software, San Diego, CA). All data were expressed as mean ± SEM. One-way analysis of variance followed by post hoc analysis (Bonferroni test) was used and a p < 0.05 was considered statistically significant.