Tight junction formation by a claudin mutant lacking the COOH‐terminal PDZ domain‐binding motif
Claudin‐based tight junctions (TJs) are formed at the most apical part of cell–cell contacts in epithelial cells. Previous studies suggest that scaffolding proteins ZO‐1 and ZO‐2 (ZO proteins) determine the location of TJs by interacting with claudins, but this idea is not conclusive. To address the...
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Published in | Annals of the New York Academy of Sciences Vol. 1516; no. 1; pp. 85 - 94 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Subscription Services, Inc
01.10.2022
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Claudin‐based tight junctions (TJs) are formed at the most apical part of cell–cell contacts in epithelial cells. Previous studies suggest that scaffolding proteins ZO‐1 and ZO‐2 (ZO proteins) determine the location of TJs by interacting with claudins, but this idea is not conclusive. To address the role of the ZO proteins binding to claudins at TJs, a COOH‐terminal PDZ domain binding motif‐deleted claudin‐3 mutant, which lacks the ZO protein binding, was stably expressed in claudin‐deficient MDCK cells. The COOH‐terminus‐deleted claudin‐3 was localized at the apicolateral region similar to full‐length claudin‐3. Consistently, freeze‐fracture electron microscopy revealed that the COOH‐terminus‐deleted claudin‐3‐expressing cells reconstituted belts of TJs at the most apical region of the lateral membrane and restored functional epithelial barriers. These results suggest that the interaction of claudins with ZO proteins is not a prerequisite for TJ formation at the most apical part of cell–cell contacts.
A claudin‐3 mutant lacking its COOH‐terminal PDZ domain‐binding motif generated functional tight junctions at the apicolateral region of cell‐cell contacts in claudin‐deficient MDCK cells, suggesting that the location of tight junctions is not determined by claudin interaction with scaffold proteins. |
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Bibliography: | Sachiko Fujiwara, Thanh Phuong Nguyen, and Kyoko Furuse contributed equally to this work. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0077-8923 1749-6632 1749-6632 |
DOI: | 10.1111/nyas.14881 |