MAL regulates clathrin-mediated endocytosis at the apical surface of Madin–Darby canine kidney cells
Open Access
- 6 October 2003
- journal article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 163 (1) , 155-164
- https://doi.org/10.1083/jcb.200304053
Abstract
MAL is an integral protein component of the machinery for apical transport in epithelial Madin–Darby canine kidney (MDCK) cells. To maintain its distribution, MAL cycles continuously between the plasma membrane and the Golgi complex. The clathrin-mediated route for apical internalization is known to differ from that at the basolateral surface. Herein, we report that MAL depends on the clathrin pathway for apical internalization. Apically internalized polymeric Ig receptor (pIgR), which uses clathrin for endocytosis, colocalized with internalized MAL in the same apical vesicles. Time-lapse confocal microscopic analysis revealed cotransport of pIgR and MAL in the same endocytic structures. Immunoelectron microscopic analysis evidenced colabeling of MAL with apically labeled pIgR in pits and clathrin-coated vesicles. Apical internalization of pIgR was abrogated in cells with reduced levels of MAL, whereas this did not occur either with its basolateral entry or the apical internalization of glycosylphosphatidylinositol-anchored proteins, which does not involve clathrin. Therefore, MAL is critical for efficient clathrin-mediated endocytosis at the apical surface in MDCK cells.Keywords
This publication has 31 references indexed in Scilit:
- MARVEL: a conserved domain involved in membrane apposition eventsTrends in Biochemical Sciences, 2002
- MAL2, a novel raft protein of the MAL family, is an essential component of the machinery for transcytosis in hepatoma HepG2 cellsThe Journal of cell biology, 2002
- Peri-Golgi vesicles contain retrograde but not anterograde proteins consistent with the cisternal progression model of intra-Golgi transportThe Journal of cell biology, 2001
- MAL Mediates Apical Transport of Secretory Proteins in Polarized Epithelial Madin-Darby Canine Kidney CellsJournal of Biological Chemistry, 2001
- Vesicular Tubular Clusters between the ER and Golgi Mediate Concentration of Soluble Secretory Proteins by Exclusion from COPI-Coated VesiclesPublished by Elsevier ,1999
- Recombinant Expression of the MAL Proteolipid, a Component of Glycolipid-enriched Membrane Microdomains, Induces the Formation of Vesicular Structures in Insect CellsPublished by Elsevier ,1997
- Structural and Biochemical Similarities Reveal a Family of Proteins Related to the MAL Proteolipid, a Component of Detergent-Insoluble Membrane MicrodomainsBiochemical and Biophysical Research Communications, 1997
- Apical and basolateral endosomes of MDCK cells are interconnected and contain a polarized sorting mechanism.The Journal of cell biology, 1996
- Apical and basolateral coated pits of MDCK cells differ in their rates of maturation into coated vesicles, but not in the ability to distinguish between mutant hemagglutinin proteins with different internalization signals.The Journal of cell biology, 1995
- Postendocytotic sorting of the ligand for the polymeric immunoglobulin receptor in Madin-Darby canine kidney cells.The Journal of cell biology, 1989