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First published online August 29, 2005
doi: 10.1242/10.1242/jcs.02528


Journal of Cell Science 118, 4049-4057 (2005)
Published by The Company of Biologists 2005
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Research Article

PATJ connects and stabilizes apical and lateral components of tight junctions in human intestinal cells

Didier Michel1, Jean-Pierre Arsanto1, Dominique Massey-Harroche1, Christophe Béclin2, Jan Wijnholds3 and André Le Bivic1,*

1 UMR 6156, NMDA, Institute of Developmental Biology of Marseille, Faculté des Sciences de Luminy, case 907, 13288 Marseille Cedex 09, France
2 IMVT, Faculté des Sciences de Luminy, case 907, 13288 Marseille Cedex 09, France
3 The Netherlands Ophthalmic Research Institute, Royal Netherlands Academy of Arts and Sciences, Meibergdreef 47, 1105 BA Amsterdam, The Netherlands

* Author for correspondence (e-mail: lebivic{at}ibdm.univ-mrs.fr)

Accepted 7 June 2005

The Crumbs complex that also contains the cortical proteins Stardust and DPATJ (a homologue of PATJ), is crucial for the building of epithelial monolayers in Drosophila. Although loss of function of the Crumbs or Stardust genes prevents the stabilization of a belt of adherens junctions at the apico-lateral border of the cells, no phenotype has been described for the Dpatj gene and its role in epithelial morphogenesis and polarity remains unknown. We have produced downregulated PATJ stable lines of Caco2 to clarify its role in epithelial morphogenesis. In PATJ knockdown cells, Pals1 (a Stardust homologue) is no longer associated with tight junctions whereas Crumbs3 (Crb3) is accumulated into a compartment spatially close to the apical membrane and related to early endosomes. Furthermore, occludin and ZO-3, two proteins of tight junctions are mislocalized on the lateral membrane indicating that PATJ plays a novel role in the building of tight junctions by providing a link between their lateral and apical components. Thus, PATJ stabilizes the Crb3 complex and regulates the spatial concentration of several components at the border between the apical and lateral domains.

Key words: Epithelial polarity, Tight junctions, Caco2


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