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缺血诱导的上皮极性丧失。紧密连接的作用。

Ischemia-induced loss of epithelial polarity. Role of the tight junction.

作者信息

Molitoris B A, Falk S A, Dahl R H

机构信息

Department of Medicine, University of Colorado Medical Center, Denver.

出版信息

J Clin Invest. 1989 Oct;84(4):1334-9. doi: 10.1172/JCI114302.

Abstract

In proximal tubular cells ischemia is known to result in the redistribution of apical and basolateral domain-specific lipids and proteins into the alternate surface membrane domain. Since tight junctions are required for the maintenance of surface membrane polarity, the effect of ischemia on tight junction functional integrity was investigated. In vivo microperfusion of early loops of proximal tubules with ruthenium red (0.2%) in glutaraldehyde (2%) was used to gain selective access to and outline the apical surface membrane. Under control situations ruthenium red penetrated less than 10% of the tight junctions. After 5, 15, and 30 min of ischemia, however, there was a successive stepwise increase in tight junction penetration by ruthenium red to 29, 50, and 62%, respectively. This was associated with the rapid duration-dependent redistribution of basolateral membrane domain-specific lipids and NaK-ATPase into the apical membrane domain. Taken together, these data indicate that during ischemia proximal tubule tight junctions open, which in turn leads to the lateral intramembranous diffusion of membrane components into the alternate surface membrane domain.

摘要

已知在近端肾小管细胞中,缺血会导致顶端和基底外侧区域特异性脂质和蛋白质重新分布到另一侧的表面膜区域。由于紧密连接对于维持表面膜极性是必需的,因此研究了缺血对紧密连接功能完整性的影响。使用在戊二醛(2%)中加入钌红(0.2%)对近端小管早期袢进行体内微灌注,以选择性地进入并勾勒出顶端表面膜。在对照情况下,钌红穿透少于10%的紧密连接。然而,在缺血5、15和30分钟后,钌红对紧密连接的穿透率依次逐步增加,分别达到29%、50%和62%。这与基底外侧膜区域特异性脂质和钠钾ATP酶迅速的、持续时间依赖性地重新分布到顶端膜区域有关。综上所述,这些数据表明在缺血期间近端小管紧密连接开放,这进而导致膜成分在膜内横向扩散到另一侧的表面膜区域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f4/329795/895c9d95e04e/jcinvest00485-0291-a.jpg

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