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平滑肌细胞迁移与增殖:高血压中的致动脉粥样硬化机制

Smooth muscle cell migration and proliferation: atherogenic mechanisms in hypertension.

作者信息

Grünwald J, Chobanian A V, Haudenschild C C

机构信息

Institute for Arteriosclerosis Research at the University of Münster, F.R.G.

出版信息

Atherosclerosis. 1987 Oct;67(2-3):215-21. doi: 10.1016/0021-9150(87)90281-4.

Abstract

The proliferative and migratory behavior of explanted rat aortic smooth muscle cells (SMC) was investigated in cells obtained from either 24-week-old normotensive Wistar-Kyoto (WKY) or age-matched spontaneously hypertensive (SHR) rats. Time lapse video analysis of primary SMC growth in the presence of 10% serum revealed that interdivision times of cells from SHR were significantly shorter than those from WKY. Differences in the proliferative capacity of these cells were still present after two subcultivations, as analyzed by conventional growth curves. In contrast to the proliferative behavior, no differences in the migratory characteristics of SMC could be detected in a migration assay analyzing the SMC outgrowth of standardized aortic explants under low serum conditions (0.1% fetal bovine serum). It has been shown that another model of hypertension, the 4 week DOC/salt hypertensive rat results in a different reaction of SMC. Therefore, it can be considered that the extent of the potentially atherogenic alterations of SMC function in hypertension is dependent on the type, duration and the rate of increase of hypertension.

摘要

研究了从24周龄的正常血压Wistar-Kyoto(WKY)大鼠或年龄匹配的自发性高血压(SHR)大鼠获取的主动脉平滑肌细胞(SMC)的增殖和迁移行为。对在10%血清存在下原代SMC生长进行的延时视频分析显示,SHR来源的细胞分裂间期显著短于WKY来源的细胞。通过传统生长曲线分析,在两次传代培养后,这些细胞的增殖能力差异仍然存在。与增殖行为相反,在低血清条件(0.1%胎牛血清)下分析标准化主动脉外植体的SMC生长的迁移试验中,未检测到SMC迁移特性的差异。已经表明,另一种高血压模型,即4周的去氧皮质酮/盐高血压大鼠会导致SMC的不同反应。因此,可以认为高血压中SMC功能潜在致动脉粥样硬化改变的程度取决于高血压的类型、持续时间和升高速率。

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