首页 | 本学科首页   官方微博 | 高级检索  
     

基于V-ATPase a3转运蛋白探讨骨质疏松症的分子机制
引用本文:宋敏 陈秉雄,陈秉虎 柴居堂 董万涛 蒋宜伟. 基于V-ATPase a3转运蛋白探讨骨质疏松症的分子机制[J]. 中国骨质疏松杂志, 2014, 0(6): 706-710
作者姓名:宋敏 陈秉雄  陈秉虎 柴居堂 董万涛 蒋宜伟
作者单位:甘肃中医学院;临洮县人民医院;甘肃中医学院附属医院;
基金项目:甘肃省财政厅基本科研项目(BH2010-028);甘肃省自然科学基金项目(1010RJZA160)
摘    要:目的存在于破骨细胞的皱褶缘上的V-ATPase a3转运蛋白在骨质疏松症的骨吸收中发挥着重要作用。V-ATPase a3转运蛋白将H+逆浓度梯度转运到密闭区,溶解无机矿物质,为水解酶如CAⅡ、CATK、MMPs等提供酸性环境,抑制V-ATPase a3转运蛋白已成为治疗骨质疏松症的新靶标;并深化对CAⅡ、CATK、MMPs等水解酶阻滞剂的认识,从而多渠道、多方位、多靶点地拓展骨质疏松症的治疗。

关 键 词:V-ATPase a  破骨细胞  骨质疏松症

Exploration of the molecular mechanism of osteoporosis based on the V-ATPase a3 transporter
SONG Min,CHEN Bingxiong,CHEN Binghu,CHAI Jutang,DONG Wantao,JIANG Yiwei.. Exploration of the molecular mechanism of osteoporosis based on the V-ATPase a3 transporter[J]. Chinese Journal of Osteoporosis, 2014, 0(6): 706-710
Authors:SONG Min  CHEN Bingxiong  CHEN Binghu  CHAI Jutang  DONG Wantao  JIANG Yiwei.
Abstract:V-ATPase a3 transporter, which exists in the ruffled border of osteoclasts, plays an important role in bone resorption in osteoporosis. It can transport H+ to the closed area to form a high H+ concentration zone, thus dissolving inorganic minerals and providing an acidic environment for hydrolytic enzymes including CA II, CATK, and MMPs. The inhibitor of the V-ATPase a3 transporter has become the new target for the treatment of osteoporosis. Deep understanding of the hydrolytic enzymes including CA II, CATK, and MMPs can provide new ideas concerning the multi-channel, multi-dimension, and multi-target treatment of the osteoporosis.
Keywords:V-ATPase a3   Osteoclast   Osteoporosis
本文献已被 CNKI 等数据库收录!
点击此处可从《中国骨质疏松杂志》浏览原始摘要信息
点击此处可从《中国骨质疏松杂志》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号