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Role of adenomatous polyposis coli in proliferation and differentiation of colon epithelial cells in organoid culture
Adenomatous polyposis coli (APC) is a tumor-suppressing protein whose inactivation triggers the formation of colorectal polyps. Numerous studies using cell lines or genetically engineered mice have revealed its role in suppressing Wnt/β-catenin signaling pathway and regulating cell proliferation and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889860/ https://www.ncbi.nlm.nih.gov/pubmed/33597597 http://dx.doi.org/10.1038/s41598-021-83590-6 |
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author | Yamazaki, Daisuke Hashizume, Osamu Taniguchi, Shiho Funato, Yosuke Miki, Hiroaki |
author_facet | Yamazaki, Daisuke Hashizume, Osamu Taniguchi, Shiho Funato, Yosuke Miki, Hiroaki |
author_sort | Yamazaki, Daisuke |
collection | PubMed |
description | Adenomatous polyposis coli (APC) is a tumor-suppressing protein whose inactivation triggers the formation of colorectal polyps. Numerous studies using cell lines or genetically engineered mice have revealed its role in suppressing Wnt/β-catenin signaling pathway and regulating cell proliferation and differentiation. Here, we performed genetic analyses of APC using a three-dimensional organoid culture of mouse colon epithelia, which enables the detailed examination of epithelial properties. Analyses of Apc-knockout colon organoids not only confirmed the importance of APC in suppressing Wnt/β-catenin signaling and regulating cell differentiation, but also revealed several novel features: a significant decrease in proliferating speed and an increase in cross-sectional area of cells. Moreover, we found a significant number of lysozyme-positive Paneth-like cells, which were never observed in wild-type colon tissues or organoids, but have been reported to emerge in colon cancers. Therefore, APC autonomously suppresses ectopic differentiation into lysozyme-positive cells, specifically in the colon epithelia. Colon organoids would be an ideal material to investigate the molecular mechanism and biological importance of the ectopic differentiation associated with cancer development. |
format | Online Article Text |
id | pubmed-7889860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78898602021-02-22 Role of adenomatous polyposis coli in proliferation and differentiation of colon epithelial cells in organoid culture Yamazaki, Daisuke Hashizume, Osamu Taniguchi, Shiho Funato, Yosuke Miki, Hiroaki Sci Rep Article Adenomatous polyposis coli (APC) is a tumor-suppressing protein whose inactivation triggers the formation of colorectal polyps. Numerous studies using cell lines or genetically engineered mice have revealed its role in suppressing Wnt/β-catenin signaling pathway and regulating cell proliferation and differentiation. Here, we performed genetic analyses of APC using a three-dimensional organoid culture of mouse colon epithelia, which enables the detailed examination of epithelial properties. Analyses of Apc-knockout colon organoids not only confirmed the importance of APC in suppressing Wnt/β-catenin signaling and regulating cell differentiation, but also revealed several novel features: a significant decrease in proliferating speed and an increase in cross-sectional area of cells. Moreover, we found a significant number of lysozyme-positive Paneth-like cells, which were never observed in wild-type colon tissues or organoids, but have been reported to emerge in colon cancers. Therefore, APC autonomously suppresses ectopic differentiation into lysozyme-positive cells, specifically in the colon epithelia. Colon organoids would be an ideal material to investigate the molecular mechanism and biological importance of the ectopic differentiation associated with cancer development. Nature Publishing Group UK 2021-02-17 /pmc/articles/PMC7889860/ /pubmed/33597597 http://dx.doi.org/10.1038/s41598-021-83590-6 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yamazaki, Daisuke Hashizume, Osamu Taniguchi, Shiho Funato, Yosuke Miki, Hiroaki Role of adenomatous polyposis coli in proliferation and differentiation of colon epithelial cells in organoid culture |
title | Role of adenomatous polyposis coli in proliferation and differentiation of colon epithelial cells in organoid culture |
title_full | Role of adenomatous polyposis coli in proliferation and differentiation of colon epithelial cells in organoid culture |
title_fullStr | Role of adenomatous polyposis coli in proliferation and differentiation of colon epithelial cells in organoid culture |
title_full_unstemmed | Role of adenomatous polyposis coli in proliferation and differentiation of colon epithelial cells in organoid culture |
title_short | Role of adenomatous polyposis coli in proliferation and differentiation of colon epithelial cells in organoid culture |
title_sort | role of adenomatous polyposis coli in proliferation and differentiation of colon epithelial cells in organoid culture |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889860/ https://www.ncbi.nlm.nih.gov/pubmed/33597597 http://dx.doi.org/10.1038/s41598-021-83590-6 |
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