期刊
RENAL FAILURE
卷 31, 期 4, 页码 313-319出版社
TAYLOR & FRANCIS LTD
DOI: 10.1080/08860220902875182
关键词
advanced oxidation protein products; vascular smooth muscle cell; differentiation; vascular calcification; oxidative stress; ERK pathway
Vascular calcification is an actively regulated process similar to bone formation. Advanced oxidation protein products (AOPPs) have been demonstrated to be novel markers of oxidant-mediated protein damage. The present study investigated the role of AOPPs in inducing osteoblastic trans-differentiation and calcification of smooth muscle cells in vitro. We found that AOPPs directly increased the calcium deposition and expression of core binding factor-1 (CBF-1) and osteopontin (OPN) and significantly decreased SM--actin expression in human aortic smooth muscle cells (HASMCs). AOPPs increased intracellular oxidative stress, which was inhibited by vitamin E. Vitamin E also inhibited AOPP-induced calcium content and osteoblast differentiation of HASMCs. Furthermore, the inhibitor of ERK significantly suppressed the effects of AOPPs on calcification and osteoblast marker expression. These findings suggest that AOPPs induce vascular calcification by promoting osteoblast differentiation of smooth muscle cells via oxidative stress and ERK pathway.
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