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The desmosome is a mesoscale lipid raft–like membrane domain
Desmogleins (Dsgs) are cadherin family adhesion molecules essential for epidermal integrity. Previous studies have shown that desmogleins associate with lipid rafts, but the significance of this association was not clear. Here, we report that the desmoglein transmembrane domain (TMD) is the primary...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6724694/ https://www.ncbi.nlm.nih.gov/pubmed/30943110 http://dx.doi.org/10.1091/mbc.E18-10-0649 |
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author | Lewis, Joshua D. Caldara, Amber L. Zimmer, Stephanie E. Stahley, Sara N. Seybold, Anna Strong, Nicole L. Frangakis, Achilleas S. Levental, Ilya Wahl, James K. Mattheyses, Alexa L. Sasaki, Takashi Nakabayashi, Kazuhiko Hata, Kenichiro Matsubara, Yoichi Ishida-Yamamoto, Akemi Amagai, Masayuki Kubo, Akiharu Kowalczyk, Andrew P. |
author_facet | Lewis, Joshua D. Caldara, Amber L. Zimmer, Stephanie E. Stahley, Sara N. Seybold, Anna Strong, Nicole L. Frangakis, Achilleas S. Levental, Ilya Wahl, James K. Mattheyses, Alexa L. Sasaki, Takashi Nakabayashi, Kazuhiko Hata, Kenichiro Matsubara, Yoichi Ishida-Yamamoto, Akemi Amagai, Masayuki Kubo, Akiharu Kowalczyk, Andrew P. |
author_sort | Lewis, Joshua D. |
collection | PubMed |
description | Desmogleins (Dsgs) are cadherin family adhesion molecules essential for epidermal integrity. Previous studies have shown that desmogleins associate with lipid rafts, but the significance of this association was not clear. Here, we report that the desmoglein transmembrane domain (TMD) is the primary determinant of raft association. Further, we identify a novel mutation in the DSG1 TMD (G562R) that causes severe dermatitis, multiple allergies, and metabolic wasting syndrome. Molecular modeling predicts that this G-to-R mutation shortens the DSG1 TMD, and experiments directly demonstrate that this mutation compromises both lipid raft association and desmosome incorporation. Finally, cryo-electron tomography indicates that the lipid bilayer within the desmosome is ∼10% thicker than adjacent regions of the plasma membrane. These findings suggest that differences in bilayer thickness influence the organization of adhesion molecules within the epithelial plasma membrane, with cadherin TMDs recruited to the desmosome via the establishment of a specialized mesoscale lipid raft–like membrane domain. |
format | Online Article Text |
id | pubmed-6724694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-67246942019-09-06 The desmosome is a mesoscale lipid raft–like membrane domain Lewis, Joshua D. Caldara, Amber L. Zimmer, Stephanie E. Stahley, Sara N. Seybold, Anna Strong, Nicole L. Frangakis, Achilleas S. Levental, Ilya Wahl, James K. Mattheyses, Alexa L. Sasaki, Takashi Nakabayashi, Kazuhiko Hata, Kenichiro Matsubara, Yoichi Ishida-Yamamoto, Akemi Amagai, Masayuki Kubo, Akiharu Kowalczyk, Andrew P. Mol Biol Cell Articles Desmogleins (Dsgs) are cadherin family adhesion molecules essential for epidermal integrity. Previous studies have shown that desmogleins associate with lipid rafts, but the significance of this association was not clear. Here, we report that the desmoglein transmembrane domain (TMD) is the primary determinant of raft association. Further, we identify a novel mutation in the DSG1 TMD (G562R) that causes severe dermatitis, multiple allergies, and metabolic wasting syndrome. Molecular modeling predicts that this G-to-R mutation shortens the DSG1 TMD, and experiments directly demonstrate that this mutation compromises both lipid raft association and desmosome incorporation. Finally, cryo-electron tomography indicates that the lipid bilayer within the desmosome is ∼10% thicker than adjacent regions of the plasma membrane. These findings suggest that differences in bilayer thickness influence the organization of adhesion molecules within the epithelial plasma membrane, with cadherin TMDs recruited to the desmosome via the establishment of a specialized mesoscale lipid raft–like membrane domain. The American Society for Cell Biology 2019-06-01 /pmc/articles/PMC6724694/ /pubmed/30943110 http://dx.doi.org/10.1091/mbc.E18-10-0649 Text en © 2019 Lewis, Caldara, 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 Lewis, Joshua D. Caldara, Amber L. Zimmer, Stephanie E. Stahley, Sara N. Seybold, Anna Strong, Nicole L. Frangakis, Achilleas S. Levental, Ilya Wahl, James K. Mattheyses, Alexa L. Sasaki, Takashi Nakabayashi, Kazuhiko Hata, Kenichiro Matsubara, Yoichi Ishida-Yamamoto, Akemi Amagai, Masayuki Kubo, Akiharu Kowalczyk, Andrew P. The desmosome is a mesoscale lipid raft–like membrane domain |
title | The desmosome is a mesoscale lipid raft–like membrane domain |
title_full | The desmosome is a mesoscale lipid raft–like membrane domain |
title_fullStr | The desmosome is a mesoscale lipid raft–like membrane domain |
title_full_unstemmed | The desmosome is a mesoscale lipid raft–like membrane domain |
title_short | The desmosome is a mesoscale lipid raft–like membrane domain |
title_sort | desmosome is a mesoscale lipid raft–like membrane domain |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6724694/ https://www.ncbi.nlm.nih.gov/pubmed/30943110 http://dx.doi.org/10.1091/mbc.E18-10-0649 |
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