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Differential expression of p120-catenin 1 and 3 isoforms in epithelial tissues
P120 catenin (p120) is a non-redundant master regulatory protein of cadherin-based cell-cell junctions, intracellular signaling, and tissue homeostasis and repair. Alternative splicing can generate p120 isoforms 1 and 3 (p120-1 and p120-3), which are implicated in non-overlapping functions by differ...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331582/ https://www.ncbi.nlm.nih.gov/pubmed/30643202 http://dx.doi.org/10.1038/s41598-018-36889-w |
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author | Venhuizen, Jan-Hendrik Sommer, Sebastian Span, Paul N. Friedl, Peter Zegers, Mirjam M. |
author_facet | Venhuizen, Jan-Hendrik Sommer, Sebastian Span, Paul N. Friedl, Peter Zegers, Mirjam M. |
author_sort | Venhuizen, Jan-Hendrik |
collection | PubMed |
description | P120 catenin (p120) is a non-redundant master regulatory protein of cadherin-based cell-cell junctions, intracellular signaling, and tissue homeostasis and repair. Alternative splicing can generate p120 isoforms 1 and 3 (p120-1 and p120-3), which are implicated in non-overlapping functions by differential expression regulation and unique interactions in different cell types, with often predominant expression of p120-1 in mesenchymal cells, and p120-3 generally prevalent in epithelial cells. However, the lack of specific p120-3 protein detection has precluded analysis of their relative abundance in tissues. Here, we have developed a p120-3 isoform-specific antibody and analyzed the p120-3 localization relative to p120-1 in human tissues. p120-3 but not p120-1 is highly expressed in cell-cell junctions of simple gastrointestinal epithelia such as colon and stomach, and the acini of salivary glands and the pancreas. Conversely, the basal layer of the epidermis and hair follicles expressed p120-1 with reduced p120-3, whereas most other epithelia co-expressed p120-3 and p120-1, including bronchial epithelia and mammary luminal epithelial cells. These data provide an inventory of tissue-specific p120 isoform expression and suggest a link between p120 isoform expression and epithelial differentiation. |
format | Online Article Text |
id | pubmed-6331582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63315822019-01-16 Differential expression of p120-catenin 1 and 3 isoforms in epithelial tissues Venhuizen, Jan-Hendrik Sommer, Sebastian Span, Paul N. Friedl, Peter Zegers, Mirjam M. Sci Rep Article P120 catenin (p120) is a non-redundant master regulatory protein of cadherin-based cell-cell junctions, intracellular signaling, and tissue homeostasis and repair. Alternative splicing can generate p120 isoforms 1 and 3 (p120-1 and p120-3), which are implicated in non-overlapping functions by differential expression regulation and unique interactions in different cell types, with often predominant expression of p120-1 in mesenchymal cells, and p120-3 generally prevalent in epithelial cells. However, the lack of specific p120-3 protein detection has precluded analysis of their relative abundance in tissues. Here, we have developed a p120-3 isoform-specific antibody and analyzed the p120-3 localization relative to p120-1 in human tissues. p120-3 but not p120-1 is highly expressed in cell-cell junctions of simple gastrointestinal epithelia such as colon and stomach, and the acini of salivary glands and the pancreas. Conversely, the basal layer of the epidermis and hair follicles expressed p120-1 with reduced p120-3, whereas most other epithelia co-expressed p120-3 and p120-1, including bronchial epithelia and mammary luminal epithelial cells. These data provide an inventory of tissue-specific p120 isoform expression and suggest a link between p120 isoform expression and epithelial differentiation. Nature Publishing Group UK 2019-01-14 /pmc/articles/PMC6331582/ /pubmed/30643202 http://dx.doi.org/10.1038/s41598-018-36889-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Venhuizen, Jan-Hendrik Sommer, Sebastian Span, Paul N. Friedl, Peter Zegers, Mirjam M. Differential expression of p120-catenin 1 and 3 isoforms in epithelial tissues |
title | Differential expression of p120-catenin 1 and 3 isoforms in epithelial tissues |
title_full | Differential expression of p120-catenin 1 and 3 isoforms in epithelial tissues |
title_fullStr | Differential expression of p120-catenin 1 and 3 isoforms in epithelial tissues |
title_full_unstemmed | Differential expression of p120-catenin 1 and 3 isoforms in epithelial tissues |
title_short | Differential expression of p120-catenin 1 and 3 isoforms in epithelial tissues |
title_sort | differential expression of p120-catenin 1 and 3 isoforms in epithelial tissues |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331582/ https://www.ncbi.nlm.nih.gov/pubmed/30643202 http://dx.doi.org/10.1038/s41598-018-36889-w |
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