Endothelial adherens junctions control tight junctions by VE-cadherin-mediated upregulation of claudin-5

被引:541
作者
Taddei, Andrea [1 ]
Giampietro, Costanza [1 ]
Conti, Annarita [1 ]
Orsenigo, Fabrizio [1 ]
Breviario, Ferruccio [2 ]
Pirazzoli, Valentina [1 ]
Potente, Michael [3 ]
Daly, Christopher [4 ]
Dimmeler, Stefanie [3 ]
Dejana, Elisabetta [1 ,2 ,5 ]
机构
[1] FIRC Inst Mol Oncol, I-20139 Milan, Italy
[2] Mario Negri Inst Pharmacol Res, I-20156 Milan, Italy
[3] Univ Frankfurt, Dept Internal Med 3, D-60590 Frankfurt, Germany
[4] Regeneron Pharmaceut Inc, Tarrytown, NY 10591 USA
[5] Univ Milan, Sch Sci, Dept Biomol Sci & Biotechnol, I-20133 Milan, Italy
关键词
D O I
10.1038/ncb1752
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Intercellular junctions mediate adhesion and communication between adjoining cells. Although formed by different molecules, tight junctions (TJs) and adherens junctions (AJs) are functionally and structurally linked, but the signalling pathways behind this interaction are unknown. Here we describe a cell-specific mechanism of crosstalk between these two types of structure. We show that endothelial VE-cadherin at AJs upregulates the gene encoding the TJ adhesive protein claudin-5. This effect requires the release of the inhibitory activity of forkhead box factor FoxO1 and the Tcf-4-beta-catenin transcriptional repressor complex. Vascular endothelial (VE)-cadherin acts by inducing the phosphorylation of FoxO1 through Akt activation and by limiting the translocation of beta-catenin to the nucleus. These results offer a molecular basis for the link between AJs and TJs and explain why VE-cadherin inhibition may cause a marked increase in permeability.
引用
收藏
页码:923 / 934
页数:12
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