Modulation of the epithelial barrier by dexamethasone and prolactin in cultured Madin-Darby canine kidney (MDCK) cells

被引:24
|
作者
Peixoto, EBMI [1 ]
Collares-Buzato, CB [1 ]
机构
[1] Univ Estadual Campinas, UNICAMP, Dept Histol & Embryol, Inst Biol, BR-13083970 Campinas, SP, Brazil
关键词
epithelial barrier; tight junction; dexamethasone; prolactin; MDCK cell line; kidney; junctional proteins;
D O I
10.1016/j.cellbi.2005.08.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glucocorticoids and prolactin (PRL) have a direct effect on the formation and maintenance of tight junctions (TJs) in cultured endothelial and mammary gland epithelial cells. In this work, we investigated the effect of a synthetic glucocorticoid dexamethasone (DEX) and PRL on the paracellular barrier function in MDCK renal epithelial cells. DEX (4 mu M) + PRL (2 mu g/ml) and DEX alone increased significantly the transepithelial electrical resistance after chronic treatment (4 days) of confluent MDCK monolayers or after 24 h treatment of subconfluent monolayers. Immunoblotting and immunocytochemistry revealed no changes in the expression and distribution of TJ-associated proteins occludin, ZO-1 and claudin-1 in confluent monolayers after hormone addition. However, a marked increase in junctional content for occludin and ZO-1 with no changes in their total expression was observed in subconfluent MDCK monolayers 24 h exposed to DEX or DEX + PRL. No change in cell proliferation/growth was detected at subconfluent conditions following hormone treatment. An increase in the total number of viable cells was observed only in confluent MDCK monolayers after exposure to DEX + PRL suggesting that the main effect of these hormones on already established barrier may be associated with the inhibition of cell death. In Conclusion, our data Suggest that these hormones (specially dexamethasone) have an effect on TJ structure and function only during the formation of MDCK epithelial barrier by probably modulating the localization, stability or assembly of TJ proteins to membrane sites of intercellular contact. (c) 2005 International Federation for Cell Biology. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:101 / 113
页数:13
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