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内皮糖萼响应流体剪切应力的适应性重塑。

The adaptive remodeling of endothelial glycocalyx in response to fluid shear stress.

作者信息

Zeng Ye, Tarbell John M

机构信息

Department of Biomedical Engineering, The City College of New York, New York, New York, United States of America ; Institute of Biomedical Engineering, School of Preclinical and Forensic Medicine, Sichuan University, Chengdu, China.

Department of Biomedical Engineering, The City College of New York, New York, New York, United States of America.

出版信息

PLoS One. 2014 Jan 20;9(1):e86249. doi: 10.1371/journal.pone.0086249. eCollection 2014.

Abstract

The endothelial glycocalyx is vital for mechanotransduction and endothelial barrier integrity. We previously demonstrated the early changes in glycocalyx organization during the initial 30 min of shear exposure. In the present study, we tested the hypothesis that long-term shear stress induces further remodeling of the glycocalyx resulting in a robust layer, and explored the responses of membrane rafts and the actin cytoskeleton. After exposure to shear stress for 24 h, the glycocalyx components heparan sulfate, chondroitin sulfate, glypican-1 and syndecan-1, were enhanced on the apical surface, with nearly uniform spatial distributions close to baseline levels that differed greatly from the 30 min distributions. Heparan sulfate and glypican-1 still clustered near the cell boundaries after 24 h of shear, but caveolin-1/caveolae and actin were enhanced and concentrated across the apical aspects of the cell. Our findings also suggest the GM1-labelled membrane rafts were associated with caveolae and glypican-1/heparan sulfate and varied in concert with these components. We conclude that remodeling of the glycocalyx to long-term shear stress is associated with the changes in membrane rafts and the actin cytoskeleton. This study reveals a space- and time- dependent reorganization of the glycocalyx that may underlie alterations in mechanotransduction mechanisms over the time course of shear exposure.

摘要

内皮糖萼对于机械转导和内皮屏障完整性至关重要。我们之前展示了在剪切力作用最初30分钟内糖萼组织的早期变化。在本研究中,我们测试了长期剪切应力诱导糖萼进一步重塑从而形成稳固层的假说,并探究了膜筏和肌动蛋白细胞骨架的反应。在暴露于剪切应力24小时后,糖萼成分硫酸乙酰肝素、硫酸软骨素、磷脂酰肌醇蛋白聚糖-1和多配体蛋白聚糖-1在顶端表面增强,其空间分布接近基线水平且几乎均匀,这与30分钟时的分布有很大不同。剪切24小时后,硫酸乙酰肝素和磷脂酰肌醇蛋白聚糖-1仍聚集在细胞边界附近,但小窝蛋白-1/小窝和肌动蛋白增强并集中在细胞顶端区域。我们的研究结果还表明,GM1标记的膜筏与小窝以及磷脂酰肌醇蛋白聚糖-1/硫酸乙酰肝素相关,并与这些成分协同变化。我们得出结论,糖萼对长期剪切应力的重塑与膜筏和肌动蛋白细胞骨架的变化有关。本研究揭示了糖萼的时空依赖性重组,这可能是剪切暴露过程中机械转导机制改变的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a753/3896483/04447e62a3a9/pone.0086249.g001.jpg

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