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培养的人肾小球微血管内皮细胞中内皮素-1对剪切应力的分泌反应。

Secretory response of endothelin-1 in cultured human glomerular microvascular endothelial cells to shear stress.

作者信息

Wang G, Cai S, Deng X, Ouyang K, Xie G, Guidoin R

机构信息

College of Bioengineering, Key Lab for Biomechanics & Tissue Engineering, State Ministry of Education, Chongqing University, Chongqing, China.

出版信息

Biorheology. 2000;37(4):291-9.

PMID:11145075
Abstract

The shear-induced secretory response of endothelin-1 (ET-1) by human microvascular endothelial cells was studied using paired human glomerular microvascular endothelial cell (HGMEC) cultured monolayers exposed to steady-state laminar shear stress for up to 10 hours. The first cell monolayer was subjected to a shear stress of 0.65 N m-2 and the second, 1.3 N m-2. ET-1 secretion was determined by radioimmunoassay. Over 10 hours of shear, the total cumulative secretion of ET-1 was 237.4 pg/cm2 for the monolayer exposed to 1.3 N m-2 and 143.6 pg/cm2 for the monolayer exposed to 0.65 N m-2. The average ET-1 secretion rate was 20.90 +/- 2.15 and 12.45 +/- 1.05 pg/cm2.h at 0.65 N m-2 and 1.3 N m-2, respectively. The results showed that ET-1 secretion varied with the time of shear in a nonlinear fashion. Although the level of shear stress affected the absolute value of ET-1 cumulative secretion and secretion rate, the major secretion period for both monolayers occurred between 2.0 and 8.0 hours, with the peak secretion rate occurring at approximately 5 hours. Thus, the response of cultured human microvascular endothelial cells to shear stress differed from that of large vessel endothelial cell cultures in terms of ET-1 secretion. In addition to the level of shear stress, the time of shear was also an important determinant of ET-1 secretion. Consequently, the heterogeneity of vascular endothelial cells and the time of shear should both be considered in future research on the secretion of vascular endothelial cell cultures.

摘要

利用成对的人肾小球微血管内皮细胞(HGMEC)培养单层,使其暴露于稳态层流剪切应力下长达10小时,研究了人微血管内皮细胞对内皮素-1(ET-1)的剪切诱导分泌反应。第一个细胞单层承受0.65 N m-2的剪切应力,第二个承受1.3 N m-2的剪切应力。通过放射免疫测定法测定ET-1分泌。在10小时的剪切过程中,暴露于1.3 N m-2的单层ET-1的总累积分泌量为237.4 pg/cm2,暴露于0.65 N m-2的单层为143.6 pg/cm2。在0.65 N m-2和1.3 N m-2时,ET-1的平均分泌率分别为20.90±2.15和12.45±1.05 pg/cm2·h。结果表明,ET-1分泌随剪切时间呈非线性变化。尽管剪切应力水平影响ET-1累积分泌和分泌率的绝对值,但两个单层的主要分泌期均出现在2.0至8.0小时之间,峰值分泌率出现在约5小时。因此,在ET-1分泌方面,培养的人微血管内皮细胞对剪切应力的反应与大血管内皮细胞培养的反应不同。除了剪切应力水平外,剪切时间也是ET-1分泌的重要决定因素。因此,在未来关于血管内皮细胞培养物分泌的研究中,应同时考虑血管内皮细胞的异质性和剪切时间。

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