Novel function for AP-1B during cell migration.


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
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

2475-2493

Subventions

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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Auteurs

Margaret Johnson Kell (MJ)

Department of Cell and Developmental Biology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611.

Su Fen Ang (SF)

Department of Cell and Developmental Biology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611.

Lucy Pigati (L)

Department of Cell and Developmental Biology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611.

Abby Halpern (A)

Department of Cell and Developmental Biology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611.

Heike Fölsch (H)

Department of Cell and Developmental Biology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611.

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Classifications MeSH