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Cyst formation in proximal renal tubules caused by dysfunction of the microtubule minus-end regulator CAMSAP3
Epithelial cells organize an ordered array of non-centrosomal microtubules, the minus ends of which are regulated by CAMSAP3. The role of these microtubules in epithelial functions, however, is poorly understood. Here, we show that the kidneys of mice in which Camsap3 is mutated develop cysts at the...
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/PMC7954811/ https://www.ncbi.nlm.nih.gov/pubmed/33712686 http://dx.doi.org/10.1038/s41598-021-85416-x |
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author | Mitsuhata, Yuto Abe, Takaya Misaki, Kazuyo Nakajima, Yuna Kiriya, Keita Kawasaki, Miwa Kiyonari, Hiroshi Takeichi, Masatoshi Toya, Mika Sato, Masamitsu |
author_facet | Mitsuhata, Yuto Abe, Takaya Misaki, Kazuyo Nakajima, Yuna Kiriya, Keita Kawasaki, Miwa Kiyonari, Hiroshi Takeichi, Masatoshi Toya, Mika Sato, Masamitsu |
author_sort | Mitsuhata, Yuto |
collection | PubMed |
description | Epithelial cells organize an ordered array of non-centrosomal microtubules, the minus ends of which are regulated by CAMSAP3. The role of these microtubules in epithelial functions, however, is poorly understood. Here, we show that the kidneys of mice in which Camsap3 is mutated develop cysts at the proximal convoluted tubules (PCTs). PCTs were severely dilated in the mutant kidneys, and they also exhibited enhanced cell proliferation. In these PCTs, epithelial cells became flattened along with perturbation of microtubule arrays as well as of certain subcellular structures such as interdigitating basal processes. Furthermore, YAP and PIEZO1, which are known as mechanosensitive regulators for cell shaping and proliferation, were activated in these mutant PCT cells. These observations suggest that CAMSAP3-mediated microtubule networks are important for maintaining the proper mechanical properties of PCT cells, and its loss triggers cell deformation and proliferation via activation of mechanosensors, resulting in the dilation of PCTs. |
format | Online Article Text |
id | pubmed-7954811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79548112021-03-15 Cyst formation in proximal renal tubules caused by dysfunction of the microtubule minus-end regulator CAMSAP3 Mitsuhata, Yuto Abe, Takaya Misaki, Kazuyo Nakajima, Yuna Kiriya, Keita Kawasaki, Miwa Kiyonari, Hiroshi Takeichi, Masatoshi Toya, Mika Sato, Masamitsu Sci Rep Article Epithelial cells organize an ordered array of non-centrosomal microtubules, the minus ends of which are regulated by CAMSAP3. The role of these microtubules in epithelial functions, however, is poorly understood. Here, we show that the kidneys of mice in which Camsap3 is mutated develop cysts at the proximal convoluted tubules (PCTs). PCTs were severely dilated in the mutant kidneys, and they also exhibited enhanced cell proliferation. In these PCTs, epithelial cells became flattened along with perturbation of microtubule arrays as well as of certain subcellular structures such as interdigitating basal processes. Furthermore, YAP and PIEZO1, which are known as mechanosensitive regulators for cell shaping and proliferation, were activated in these mutant PCT cells. These observations suggest that CAMSAP3-mediated microtubule networks are important for maintaining the proper mechanical properties of PCT cells, and its loss triggers cell deformation and proliferation via activation of mechanosensors, resulting in the dilation of PCTs. Nature Publishing Group UK 2021-03-12 /pmc/articles/PMC7954811/ /pubmed/33712686 http://dx.doi.org/10.1038/s41598-021-85416-x 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 Mitsuhata, Yuto Abe, Takaya Misaki, Kazuyo Nakajima, Yuna Kiriya, Keita Kawasaki, Miwa Kiyonari, Hiroshi Takeichi, Masatoshi Toya, Mika Sato, Masamitsu Cyst formation in proximal renal tubules caused by dysfunction of the microtubule minus-end regulator CAMSAP3 |
title | Cyst formation in proximal renal tubules caused by dysfunction of the microtubule minus-end regulator CAMSAP3 |
title_full | Cyst formation in proximal renal tubules caused by dysfunction of the microtubule minus-end regulator CAMSAP3 |
title_fullStr | Cyst formation in proximal renal tubules caused by dysfunction of the microtubule minus-end regulator CAMSAP3 |
title_full_unstemmed | Cyst formation in proximal renal tubules caused by dysfunction of the microtubule minus-end regulator CAMSAP3 |
title_short | Cyst formation in proximal renal tubules caused by dysfunction of the microtubule minus-end regulator CAMSAP3 |
title_sort | cyst formation in proximal renal tubules caused by dysfunction of the microtubule minus-end regulator camsap3 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954811/ https://www.ncbi.nlm.nih.gov/pubmed/33712686 http://dx.doi.org/10.1038/s41598-021-85416-x |
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