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上皮因子对紧密连接形态和通透性的调节作用。

Modulation of tight junction morphology and permeability by an epithelial factor.

作者信息

Jaeger M M, Dodane V, Kachar B

机构信息

Laboratory of Cellular Biology, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, Maryland 20850.

出版信息

J Membr Biol. 1994 Apr;139(1):41-8. doi: 10.1007/BF00232673.

Abstract

We report evidence of a factor secreted at the apical side of epithelial monolayers which modulates tight junction structure and permeability. This activity was detected within 4-7 days of conditioning of the apical medium by MDCK, A6 or Caco-2 epithelial cell lines cultured on permeable membranes in bipartite chambers. Apical conditioned medium (ACM), applied to the basolateral surface of a confluent monolayer, increased the transepithelial electrical resistance (TER), progressively reaching values 12-22% higher than the baseline within 5-10 min. After 40-60 min, the TER returned slowly to the basal value. This phenomenon was not observed either when using preheated ACM or the ACM filtrate obtained through a 30,000 MW cutoff membrane. The ACM maintained its activity even when applied to cell lines from different organs and species, as demonstrated when ACM from MDCK monolayers promoted an increase of 22% in the TER of Caco-2 cells. The increase of TER induced by the ACM treatment is accompanied by a change in the distribution of the number of tight junction strands, from an initial pattern, dominated mostly by junctions with one or two strands, to a new pattern after treatment dominated by junctions with two or three strands. Our results suggest the existence of a mechanism in epithelial cells that could signal leakage of apically secreted components to the basolateral side, thereby modulating the junction structure and permeability.

摘要

我们报告了上皮单层顶端分泌的一种因子的证据,该因子可调节紧密连接结构和通透性。在二分室中培养于可渗透膜上的MDCK、A6或Caco-2上皮细胞系对顶端培养基进行4-7天的预处理后,检测到了这种活性。将顶端条件培养基(ACM)应用于汇合单层的基底外侧表面,可增加跨上皮电阻(TER),在5-10分钟内逐渐达到比基线高12-22%的值。40-60分钟后,TER缓慢恢复到基础值。使用预热的ACM或通过30,000 MW截留膜获得的ACM滤液时,均未观察到这种现象。即使将ACM应用于来自不同器官和物种的细胞系,它仍保持其活性,如MDCK单层的ACM促进Caco-2细胞的TER增加22%所证明的那样。ACM处理诱导的TER增加伴随着紧密连接链数量分布的变化,从最初主要由一两条链的连接主导的模式,变为处理后由两三条链的连接主导的新模式。我们的结果表明上皮细胞中存在一种机制,该机制可能将顶端分泌成分向基底外侧的泄漏作为信号,从而调节连接结构和通透性。

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