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Proteomic analysis of desmosomes reveals novel components required for epidermal integrity
Desmosomes are cell–cell adhesions necessary for the maintenance of tissue integrity in the skin and heart. While the core components of desmosomes have been identified, peripheral components that modulate canonical or noncanonical desmosome functions still remain largely unexplored. Here we used ta...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353166/ https://www.ncbi.nlm.nih.gov/pubmed/32238101 http://dx.doi.org/10.1091/mbc.E19-09-0542 |
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author | Badu-Nkansah, Kwabena A. Lechler, Terry |
author_facet | Badu-Nkansah, Kwabena A. Lechler, Terry |
author_sort | Badu-Nkansah, Kwabena A. |
collection | PubMed |
description | Desmosomes are cell–cell adhesions necessary for the maintenance of tissue integrity in the skin and heart. While the core components of desmosomes have been identified, peripheral components that modulate canonical or noncanonical desmosome functions still remain largely unexplored. Here we used targeted proximity labeling approaches to further elaborate the desmosome proteome in epidermal keratinocytes. Quantitative mass spectrometry analysis identified all core desmosomal proteins while uncovering a diverse array of new constituents with broad molecular functions. By individually targeting the inner and outer dense plaques, we defined proteins enriched within these subcompartments. We validated a number of these novel desmosome-associated proteins and find that many are membrane proximal proteins that show a dependence on functional desmosomes for their cortical localization. We further explored the mechanism of localization and function of two novel desmosome-associated adaptor proteins enriched in the desmosome proteome, Crk and Crk-like (CrkL). These proteins interacted with Dsg1 and rely on Dsg1 and desmoplakin for robust cortical localization. Epidermal deletion of both Crk and CrkL resulted in perinatal lethality with defects in desmosome morphology and keratin organization, thus demonstrating the utility of this dataset in identifying novel proteins required for desmosome-dependent epidermal integrity. |
format | Online Article Text |
id | pubmed-7353166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73531662020-07-30 Proteomic analysis of desmosomes reveals novel components required for epidermal integrity Badu-Nkansah, Kwabena A. Lechler, Terry Mol Biol Cell Articles Desmosomes are cell–cell adhesions necessary for the maintenance of tissue integrity in the skin and heart. While the core components of desmosomes have been identified, peripheral components that modulate canonical or noncanonical desmosome functions still remain largely unexplored. Here we used targeted proximity labeling approaches to further elaborate the desmosome proteome in epidermal keratinocytes. Quantitative mass spectrometry analysis identified all core desmosomal proteins while uncovering a diverse array of new constituents with broad molecular functions. By individually targeting the inner and outer dense plaques, we defined proteins enriched within these subcompartments. We validated a number of these novel desmosome-associated proteins and find that many are membrane proximal proteins that show a dependence on functional desmosomes for their cortical localization. We further explored the mechanism of localization and function of two novel desmosome-associated adaptor proteins enriched in the desmosome proteome, Crk and Crk-like (CrkL). These proteins interacted with Dsg1 and rely on Dsg1 and desmoplakin for robust cortical localization. Epidermal deletion of both Crk and CrkL resulted in perinatal lethality with defects in desmosome morphology and keratin organization, thus demonstrating the utility of this dataset in identifying novel proteins required for desmosome-dependent epidermal integrity. The American Society for Cell Biology 2020-05-15 /pmc/articles/PMC7353166/ /pubmed/32238101 http://dx.doi.org/10.1091/mbc.E19-09-0542 Text en © 2020 Badu-Nkansah and Lechler. “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 Badu-Nkansah, Kwabena A. Lechler, Terry Proteomic analysis of desmosomes reveals novel components required for epidermal integrity |
title | Proteomic analysis of desmosomes reveals novel components required for epidermal integrity |
title_full | Proteomic analysis of desmosomes reveals novel components required for epidermal integrity |
title_fullStr | Proteomic analysis of desmosomes reveals novel components required for epidermal integrity |
title_full_unstemmed | Proteomic analysis of desmosomes reveals novel components required for epidermal integrity |
title_short | Proteomic analysis of desmosomes reveals novel components required for epidermal integrity |
title_sort | proteomic analysis of desmosomes reveals novel components required for epidermal integrity |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353166/ https://www.ncbi.nlm.nih.gov/pubmed/32238101 http://dx.doi.org/10.1091/mbc.E19-09-0542 |
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