MarvelD3 couples tight junctions to the MEKK1–JNK pathway to regulate cell behavior and survival

Author:

Steed Emily1,Elbediwy Ahmed1,Vacca Barbara1,Dupasquier Sébastien2,Hemkemeyer Sandra A.1,Suddason Tesha3,Costa Ana C.1,Beaudry Jean-Bernard2,Zihni Ceniz1,Gallagher Ewen3,Pierreux Christophe E.2,Balda Maria S.1,Matter Karl1

Affiliation:

1. Department of Cell Biology, Institute of Ophthalmology, University College London, London EC1V 9EL, England, UK

2. CELL Unit, de Duve Institute and Université Catholique de Louvain, B-1200 Brussels, Belgium

3. Department of Immunology, Imperial College London, London W12 0NN, England, UK

Abstract

MarvelD3 is a transmembrane component of tight junctions, but there is little evidence for a direct involvement in the junctional permeability barrier. Tight junctions also regulate signaling mechanisms that guide cell proliferation; however, the transmembrane components that link the junction to such signaling pathways are not well understood. In this paper, we show that MarvelD3 is a dynamic junctional regulator of the MEKK1–c-Jun NH2-terminal kinase (JNK) pathway. Loss of MarvelD3 expression in differentiating Caco-2 cells resulted in increased cell migration and proliferation, whereas reexpression in a metastatic tumor cell line inhibited migration, proliferation, and in vivo tumor formation. Expression levels of MarvelD3 inversely correlated with JNK activity, as MarvelD3 recruited MEKK1 to junctions, leading to down-regulation of JNK phosphorylation and inhibition of JNK-regulated transcriptional mechanisms. Interplay between MarvelD3 internalization and JNK activation tuned activation of MEKK1 during osmotic stress, leading to junction dissociation and cell death in MarvelD3-depleted cells. MarvelD3 thus couples tight junctions to the MEKK1–JNK pathway to regulate cell behavior and survival.

Publisher

Rockefeller University Press

Subject

Cell Biology

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