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Recycling endosomal CD133 functions as an inhibitor of autophagy at the pericentrosomal region
CD133 is a transmembranous protein that mainly localises to the plasma membrane in haematopoietic and neural stem cells as well as cancer stem cells. Although CD133 also localises to the cytoplasm, the mechanism of action and function of cytoplasmic CD133 currently remain unknown. We herein demonstr...
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/PMC6381095/ https://www.ncbi.nlm.nih.gov/pubmed/30783186 http://dx.doi.org/10.1038/s41598-019-39229-8 |
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author | Izumi, Hideki Li, Yuanyuan Shibaki, Masami Mori, Daisuke Yasunami, Michio Sato, Seiji Matsunaga, Hisashi Mae, Takao Kodama, Kenji Kamijo, Takehiko Kaneko, Yasuhiko Nakagawara, Akira |
author_facet | Izumi, Hideki Li, Yuanyuan Shibaki, Masami Mori, Daisuke Yasunami, Michio Sato, Seiji Matsunaga, Hisashi Mae, Takao Kodama, Kenji Kamijo, Takehiko Kaneko, Yasuhiko Nakagawara, Akira |
author_sort | Izumi, Hideki |
collection | PubMed |
description | CD133 is a transmembranous protein that mainly localises to the plasma membrane in haematopoietic and neural stem cells as well as cancer stem cells. Although CD133 also localises to the cytoplasm, the mechanism of action and function of cytoplasmic CD133 currently remain unknown. We herein demonstrated that when Src family kinase activity is weak, CD133 interacts with HDAC6 and is transported to the pericentrosomal region after internalization and endosome formation via the dynein-based traffic system. Pericentrosomal CD133 is then recycled to the plasma membrane via recycling endosomes. At the pericentrosomal region, endosomal CD133 captures GABARAP, an initiator of autophagy, and inhibits GABARAP-mediated ULK1 activation and the subsequent initiation of autophagy. Furthermore, pericentrosomal CD133 suppresses cell differentiation, such as primary cilium formation and neurite outgrowth, by inhibiting autophagy. Thus, the present results provide evidence to suggest that pericentrosomal CD133 has the unique property of maintaining the undifferentiated status of cells by inhibiting autophagy. |
format | Online Article Text |
id | pubmed-6381095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63810952019-02-21 Recycling endosomal CD133 functions as an inhibitor of autophagy at the pericentrosomal region Izumi, Hideki Li, Yuanyuan Shibaki, Masami Mori, Daisuke Yasunami, Michio Sato, Seiji Matsunaga, Hisashi Mae, Takao Kodama, Kenji Kamijo, Takehiko Kaneko, Yasuhiko Nakagawara, Akira Sci Rep Article CD133 is a transmembranous protein that mainly localises to the plasma membrane in haematopoietic and neural stem cells as well as cancer stem cells. Although CD133 also localises to the cytoplasm, the mechanism of action and function of cytoplasmic CD133 currently remain unknown. We herein demonstrated that when Src family kinase activity is weak, CD133 interacts with HDAC6 and is transported to the pericentrosomal region after internalization and endosome formation via the dynein-based traffic system. Pericentrosomal CD133 is then recycled to the plasma membrane via recycling endosomes. At the pericentrosomal region, endosomal CD133 captures GABARAP, an initiator of autophagy, and inhibits GABARAP-mediated ULK1 activation and the subsequent initiation of autophagy. Furthermore, pericentrosomal CD133 suppresses cell differentiation, such as primary cilium formation and neurite outgrowth, by inhibiting autophagy. Thus, the present results provide evidence to suggest that pericentrosomal CD133 has the unique property of maintaining the undifferentiated status of cells by inhibiting autophagy. Nature Publishing Group UK 2019-02-19 /pmc/articles/PMC6381095/ /pubmed/30783186 http://dx.doi.org/10.1038/s41598-019-39229-8 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 Izumi, Hideki Li, Yuanyuan Shibaki, Masami Mori, Daisuke Yasunami, Michio Sato, Seiji Matsunaga, Hisashi Mae, Takao Kodama, Kenji Kamijo, Takehiko Kaneko, Yasuhiko Nakagawara, Akira Recycling endosomal CD133 functions as an inhibitor of autophagy at the pericentrosomal region |
title | Recycling endosomal CD133 functions as an inhibitor of autophagy at the pericentrosomal region |
title_full | Recycling endosomal CD133 functions as an inhibitor of autophagy at the pericentrosomal region |
title_fullStr | Recycling endosomal CD133 functions as an inhibitor of autophagy at the pericentrosomal region |
title_full_unstemmed | Recycling endosomal CD133 functions as an inhibitor of autophagy at the pericentrosomal region |
title_short | Recycling endosomal CD133 functions as an inhibitor of autophagy at the pericentrosomal region |
title_sort | recycling endosomal cd133 functions as an inhibitor of autophagy at the pericentrosomal region |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381095/ https://www.ncbi.nlm.nih.gov/pubmed/30783186 http://dx.doi.org/10.1038/s41598-019-39229-8 |
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