High glucose promotes vascular smooth muscle cell calcification by activating WNT signaling pathway
10.3969/j.issn.1673-4254.2015.01.06
- VernacularTitle:高糖激活WNT信号通路促进血管平滑肌细胞钙化
- Author:
Jianyun YAN
1
;
Qin ZHOU
;
Huimin YU
;
Menglin HOU
;
Lihe LU
Author Information
1. 南方医科大学基础医学院组织胚胎学教研室
- Keywords:
vascular calcification;
WNT;
high glucose;
β-catenin;
vascular smooth muscle cells
- From:
Journal of Southern Medical University
2015;(1):29-33
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate whether high glucose-induced vascular calcification is associated with WNT signaling pathway. Methods An in vitro model of human vascular smooth muscle cell (VSMC) calcification was induced by exposure of the cells to high glucose. The expressions of WNT signal molecules and bone-related proteins including Cbfa1, Osx, OCN and BMP2 were analyzed with qRT-PCR, and the cell calcification was assessed by alizarin red staining. The effect of Dkk1, a WNT signaling inhibitor, on high glucose-induced cell calcification was tested with alizarin red staining and calcium content analysis. Results High glucose activated WNT signaling pathway in human VSMCs by up-regulating the expressions of WNT signal molecules including Wnt3a, Wnt7a, Fzd4 and Wisp1 mRNA by 1.86, 1.68, 2.1, and 2.3 folds, respectively, and by promoting the phosphorylation ofβ-catenin (2.70±0.22, P<0.05), a key mediator of WNT signaling pathway. Inhibition of WNT signaling pathway by Dkk1 attenuated high glucose-induced VSMC calcification and down-regulated the expression of bone-related proteins Cbfa1, Osx, OCN, and BMP2 by (51 ± 9)%, (58 ± 11)%, (56 ± 10)%, and (62 ± 10)% (P<0.01). Conclusion WNT signaling pathway is involved in high glucose-induced VSMC calcification.
