Novel function for AP-1B during cell migration.
Adaptor Protein Complex 1
/ genetics
Adaptor Protein Complex 2
/ metabolism
Adaptor Protein Complex beta Subunits
/ genetics
Adaptor Proteins, Signal Transducing
/ metabolism
Adaptor Proteins, Vesicular Transport
/ metabolism
Animals
Cell Line, Tumor
Cell Membrane
/ metabolism
Cell Movement
/ physiology
Cell Polarity
/ physiology
Clathrin
/ metabolism
Dogs
Endosomes
/ metabolism
Epithelial Cells
/ metabolism
Humans
Integrin beta1
/ metabolism
Madin Darby Canine Kidney Cells
Membrane Proteins
/ metabolism
Protein Transport
/ physiology
Journal
Molecular biology of the cell
ISSN: 1939-4586
Titre abrégé: Mol Biol Cell
Pays: United States
ID NLM: 9201390
Informations de publication
Date de publication:
15 10 2020
15 10 2020
Historique:
pubmed:
21
8
2020
medline:
8
6
2021
entrez:
21
8
2020
Statut:
ppublish
Résumé
The epithelial cell-specific clathrin adaptor protein (AP)-1B has a well-established role in polarized sorting of cargos to the basolateral membrane. Here we show that β1 integrin was dependent on AP-1B and its coadaptor, autosomal recessive hypercholesterolemia protein (ARH), for sorting to the basolateral membrane. We further demonstrate an unprecedented role for AP-1B at the basal plasma membrane during collective cell migration of epithelial sheets. During wound healing, expression of AP-1B (and ARH in AP-1B-positive cells) slowed epithelial-cell migration. We show that AP-1B colocalized with β1 integrin in focal adhesions during cell migration using confocal microscopy and total internal reflection fluorescence microscopy on fixed specimens. Further, AP-1B labeling in cell protrusions was distinct from labeling for the endocytic adaptor complex AP-2. Using stochastic optical reconstruction microscopy we identified numerous AP-1B-coated structures at or close to the basal plasma membrane in cell protrusions. In addition, immunoelectron microscopy showed AP-1B in coated pits and vesicles at the plasma membrane during cell migration. Lastly, quantitative real-time reverse transcription PCR analysis of human epithelial-derived cell lines revealed a loss of AP-1B expression in highly migratory metastatic cancer cells suggesting that AP-1B's novel role at the basal plasma membrane during cell migration might be an anticancer mechanism.
Identifiants
pubmed: 32816642
doi: 10.1091/mbc.E20-04-0256
pmc: PMC7851849
doi:
Substances chimiques
AP1B1 protein, human
0
Adaptor Protein Complex 1
0
Adaptor Protein Complex 2
0
Adaptor Protein Complex beta Subunits
0
Adaptor Proteins, Signal Transducing
0
Adaptor Proteins, Vesicular Transport
0
Clathrin
0
Integrin beta1
0
Membrane Proteins
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
2475-2493Subventions
Organisme : NIAMS NIH HHS
ID : P30 AR075049
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA060553
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM070736
Pays : United States
Organisme : NCRR NIH HHS
ID : S10 RR031680
Pays : United States
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