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Taurine inhibits osteoblastic differentiation of vascular smooth muscle cells via the ERK pathway
Authors:Xiao-bo Liao  Xin-min Zhou  Jian-ming Li  Jin-fu Yang  Zhi-ping Tan  Zhuo-wei Hu  Wei Liu  Ying Lu  Ling-qing Yuan
Institution:(1) Department of Cardiothoracic Surgery, The Second Xiang-Ya Hospital, Central South University, Changsha, Hunan, 410011, People’s Republic of China;(2) Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China;(3) Institute of Metabolism and Endocrinology, The Second Xiang-Ya Hospital, Central South University, Changsha, Hunan, 410011, People’s Republic of China
Abstract:Vascular calcification develops within atherosclerotic lesions and results from a process similar to osteogenesis. Taurine is a free β-amino acid and plays an important physiological role in mammals. We have recently demonstrated that vascular smooth muscle cells (VSMCs) express a functional taurine transporter. To evaluate the possible role of taurine in vascular calcification, we assessed its effects on osteoblastic differentiation of VSMCs in vitro. The results showed that taurine inhibited the β-glycerophosphate-induced osteoblastic differentiation of VSMCs as evidenced by both the decreasing alkaline phosphate (ALP) activity and expression of the core binding factor α1 (Cbfα1). Taurine also activated the extracellular signal-regulated protein kinase (ERK) pathway. Inhibition of ERK pathway reversed the effect of taurine on ALP activity and Cbfα1 expression. These results suggested that taurine inhibited osteoblastic differentiation of vascular cells via the ERK pathway.
Keywords:Taurine  Vascular smooth muscular cells  Extracellular signal-regulated kinases  Osteoblast
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