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Novel function for AP-1B during cell migration

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 bas...

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Autores principales: Kell, Margaret Johnson, Ang, Su Fen, Pigati, Lucy, Halpern, Abby, Fölsch, Heike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851849/
https://www.ncbi.nlm.nih.gov/pubmed/32816642
http://dx.doi.org/10.1091/mbc.E20-04-0256
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author Kell, Margaret Johnson
Ang, Su Fen
Pigati, Lucy
Halpern, Abby
Fölsch, Heike
author_facet Kell, Margaret Johnson
Ang, Su Fen
Pigati, Lucy
Halpern, Abby
Fölsch, Heike
author_sort Kell, Margaret Johnson
collection PubMed
description 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.
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spelling pubmed-78518492021-02-10 Novel function for AP-1B during cell migration Kell, Margaret Johnson Ang, Su Fen Pigati, Lucy Halpern, Abby Fölsch, Heike Mol Biol Cell Articles 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. The American Society for Cell Biology 2020-10-15 /pmc/articles/PMC7851849/ /pubmed/32816642 http://dx.doi.org/10.1091/mbc.E20-04-0256 Text en © 2020 Kell, Ang, et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License.
spellingShingle Articles
Kell, Margaret Johnson
Ang, Su Fen
Pigati, Lucy
Halpern, Abby
Fölsch, Heike
Novel function for AP-1B during cell migration
title Novel function for AP-1B during cell migration
title_full Novel function for AP-1B during cell migration
title_fullStr Novel function for AP-1B during cell migration
title_full_unstemmed Novel function for AP-1B during cell migration
title_short Novel function for AP-1B during cell migration
title_sort novel function for ap-1b during cell migration
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851849/
https://www.ncbi.nlm.nih.gov/pubmed/32816642
http://dx.doi.org/10.1091/mbc.E20-04-0256
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