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The human discs large protein 1 interacts with and maintains connexin 43 at the plasma membrane in keratinocytes
Gap junction channels, composed of connexins, allow direct cell-to-cell communication. Connexin 43 (Cx43; also known as GJA1) is widely expressed in tissues, including the epidermis. In a previous study of human papillomavirus-positive cervical epithelial tumour cells, we identified Cx43 as a bindin...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Company of Biologists Ltd
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10309592/ https://www.ncbi.nlm.nih.gov/pubmed/37288673 http://dx.doi.org/10.1242/jcs.259984 |
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author | Scott, Harry Dong, Li Stevenson, Andrew MacDonald, Alasdair I. Srinivasan, Sharmila Massimi, Paola Banks, Lawrence Martin, Patricia E. Johnstone, Scott R. Graham, Sheila V. |
author_facet | Scott, Harry Dong, Li Stevenson, Andrew MacDonald, Alasdair I. Srinivasan, Sharmila Massimi, Paola Banks, Lawrence Martin, Patricia E. Johnstone, Scott R. Graham, Sheila V. |
author_sort | Scott, Harry |
collection | PubMed |
description | Gap junction channels, composed of connexins, allow direct cell-to-cell communication. Connexin 43 (Cx43; also known as GJA1) is widely expressed in tissues, including the epidermis. In a previous study of human papillomavirus-positive cervical epithelial tumour cells, we identified Cx43 as a binding partner of the human homologue of Drosophila Discs large (Dlg1; also known as SAP97). Dlg1 is a member of the membrane associated-guanylate kinase (MAGUK) scaffolding protein family, which is known to control cell shape and polarity. Here, we show that Cx43 also interacts with Dlg1 in uninfected keratinocytes in vitro and in keratinocytes, dermal cells and adipocytes in normal human epidermis in vivo. Depletion of Dlg1 in keratinocytes did not alter Cx43 transcription but was associated with a reduction in Cx43 protein levels. Reduced Dlg1 levels in keratinocytes resulted in a reduction in Cx43 at the plasma membrane with a concomitant reduction in gap junctional intercellular communication and relocation of Cx43 to the Golgi compartment. Our data suggest a key role for Dlg1 in maintaining Cx43 at the plasma membrane in keratinocytes. |
format | Online Article Text |
id | pubmed-10309592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-103095922023-06-30 The human discs large protein 1 interacts with and maintains connexin 43 at the plasma membrane in keratinocytes Scott, Harry Dong, Li Stevenson, Andrew MacDonald, Alasdair I. Srinivasan, Sharmila Massimi, Paola Banks, Lawrence Martin, Patricia E. Johnstone, Scott R. Graham, Sheila V. J Cell Sci Research Article Gap junction channels, composed of connexins, allow direct cell-to-cell communication. Connexin 43 (Cx43; also known as GJA1) is widely expressed in tissues, including the epidermis. In a previous study of human papillomavirus-positive cervical epithelial tumour cells, we identified Cx43 as a binding partner of the human homologue of Drosophila Discs large (Dlg1; also known as SAP97). Dlg1 is a member of the membrane associated-guanylate kinase (MAGUK) scaffolding protein family, which is known to control cell shape and polarity. Here, we show that Cx43 also interacts with Dlg1 in uninfected keratinocytes in vitro and in keratinocytes, dermal cells and adipocytes in normal human epidermis in vivo. Depletion of Dlg1 in keratinocytes did not alter Cx43 transcription but was associated with a reduction in Cx43 protein levels. Reduced Dlg1 levels in keratinocytes resulted in a reduction in Cx43 at the plasma membrane with a concomitant reduction in gap junctional intercellular communication and relocation of Cx43 to the Golgi compartment. Our data suggest a key role for Dlg1 in maintaining Cx43 at the plasma membrane in keratinocytes. The Company of Biologists Ltd 2023-06-08 /pmc/articles/PMC10309592/ /pubmed/37288673 http://dx.doi.org/10.1242/jcs.259984 Text en © 2023. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Scott, Harry Dong, Li Stevenson, Andrew MacDonald, Alasdair I. Srinivasan, Sharmila Massimi, Paola Banks, Lawrence Martin, Patricia E. Johnstone, Scott R. Graham, Sheila V. The human discs large protein 1 interacts with and maintains connexin 43 at the plasma membrane in keratinocytes |
title | The human discs large protein 1 interacts with and maintains connexin 43 at the plasma membrane in keratinocytes |
title_full | The human discs large protein 1 interacts with and maintains connexin 43 at the plasma membrane in keratinocytes |
title_fullStr | The human discs large protein 1 interacts with and maintains connexin 43 at the plasma membrane in keratinocytes |
title_full_unstemmed | The human discs large protein 1 interacts with and maintains connexin 43 at the plasma membrane in keratinocytes |
title_short | The human discs large protein 1 interacts with and maintains connexin 43 at the plasma membrane in keratinocytes |
title_sort | human discs large protein 1 interacts with and maintains connexin 43 at the plasma membrane in keratinocytes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10309592/ https://www.ncbi.nlm.nih.gov/pubmed/37288673 http://dx.doi.org/10.1242/jcs.259984 |
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