Unknown

Dataset Information

0

Clathrin is a key regulator of basolateral polarity.


ABSTRACT: Clathrin-coated vesicles are vehicles for intracellular trafficking in all nucleated cells, from yeasts to humans. Many studies have demonstrated their essential roles in endocytosis and cellular signalling processes at the plasma membrane. By contrast, very few of their non-endocytic trafficking roles are known, the best characterized being the transport of hydrolases from the Golgi complex to the lysosome. Here we show that clathrin is required for polarity of the basolateral plasma membrane proteins in the epithelial cell line MDCK. Clathrin knockdown depolarized most basolateral proteins, by interfering with their biosynthetic delivery and recycling, but did not affect the polarity of apical proteins. Quantitative live imaging showed that chronic and acute clathrin knockdown selectively slowed down the exit of basolateral proteins from the Golgi complex, and promoted their mis-sorting into apical carrier vesicles. Our results demonstrate a broad requirement for clathrin in basolateral protein trafficking in epithelial cells.

SUBMITTER: Deborde S 

PROVIDER: S-EPMC4078870 | biostudies-literature | 2008 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications


Clathrin-coated vesicles are vehicles for intracellular trafficking in all nucleated cells, from yeasts to humans. Many studies have demonstrated their essential roles in endocytosis and cellular signalling processes at the plasma membrane. By contrast, very few of their non-endocytic trafficking roles are known, the best characterized being the transport of hydrolases from the Golgi complex to the lysosome. Here we show that clathrin is required for polarity of the basolateral plasma membrane p  ...[more]

Similar Datasets

| S-EPMC3690600 | biostudies-literature
| S-EPMC7658195 | biostudies-literature
| S-EPMC5266526 | biostudies-literature
| S-EPMC4067485 | biostudies-literature
| S-EPMC3132080 | biostudies-literature
| S-EPMC2920741 | biostudies-literature
| S-EPMC8569552 | biostudies-literature
2021-11-03 | PXD028919 | Pride
| S-EPMC6550009 | biostudies-literature
| S-EPMC3695649 | biostudies-literature