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In situ structure of intestinal apical surface reveals nanobristles on microvilli
Microvilli are actin-bundle-supported membrane protrusions essential for absorption, secretion, and sensation. Microvilli defects cause gastrointestinal disorders; however, mechanisms controlling microvilli formation and organization remain unresolved. Here, we study microvilli by vitrifying the Cae...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214534/ https://www.ncbi.nlm.nih.gov/pubmed/35666862 http://dx.doi.org/10.1073/pnas.2122249119 |
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author | Zhu, Hao Li, Meijing Zhao, Ruixue Li, Ming Chai, Yongping Zhu, Zhiwen Yang, Yihong Li, Wei Xie, Zhongyun Li, Xiaomin Lei, Kexin Li, Xueming Ou, Guangshuo |
author_facet | Zhu, Hao Li, Meijing Zhao, Ruixue Li, Ming Chai, Yongping Zhu, Zhiwen Yang, Yihong Li, Wei Xie, Zhongyun Li, Xiaomin Lei, Kexin Li, Xueming Ou, Guangshuo |
author_sort | Zhu, Hao |
collection | PubMed |
description | Microvilli are actin-bundle-supported membrane protrusions essential for absorption, secretion, and sensation. Microvilli defects cause gastrointestinal disorders; however, mechanisms controlling microvilli formation and organization remain unresolved. Here, we study microvilli by vitrifying the Caenorhabditis elegans larvae and mouse intestinal tissues with high-pressure freezing, thinning them with cryo-focused ion-beam milling, followed by cryo-electron tomography and subtomogram averaging. We find that many radial nanometer bristles referred to as nanobristles project from the lateral surface of nematode and mouse microvilli. The C. elegans nanobristles are 37.5 nm long and 4.5 nm wide. Nanobristle formation requires a protocadherin family protein, CDH-8, in C. elegans. The loss of nanobristles in cdh-8 mutants slows down animal growth and ectopically increases the number of Y-shaped microvilli, the putative intermediate structures if microvilli split from tips. Our results reveal a potential role of nanobristles in separating microvilli and suggest that microvilli division may help generate nascent microvilli with uniformity. |
format | Online Article Text |
id | pubmed-9214534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-92145342022-06-23 In situ structure of intestinal apical surface reveals nanobristles on microvilli Zhu, Hao Li, Meijing Zhao, Ruixue Li, Ming Chai, Yongping Zhu, Zhiwen Yang, Yihong Li, Wei Xie, Zhongyun Li, Xiaomin Lei, Kexin Li, Xueming Ou, Guangshuo Proc Natl Acad Sci U S A Biological Sciences Microvilli are actin-bundle-supported membrane protrusions essential for absorption, secretion, and sensation. Microvilli defects cause gastrointestinal disorders; however, mechanisms controlling microvilli formation and organization remain unresolved. Here, we study microvilli by vitrifying the Caenorhabditis elegans larvae and mouse intestinal tissues with high-pressure freezing, thinning them with cryo-focused ion-beam milling, followed by cryo-electron tomography and subtomogram averaging. We find that many radial nanometer bristles referred to as nanobristles project from the lateral surface of nematode and mouse microvilli. The C. elegans nanobristles are 37.5 nm long and 4.5 nm wide. Nanobristle formation requires a protocadherin family protein, CDH-8, in C. elegans. The loss of nanobristles in cdh-8 mutants slows down animal growth and ectopically increases the number of Y-shaped microvilli, the putative intermediate structures if microvilli split from tips. Our results reveal a potential role of nanobristles in separating microvilli and suggest that microvilli division may help generate nascent microvilli with uniformity. National Academy of Sciences 2022-06-06 2022-06-14 /pmc/articles/PMC9214534/ /pubmed/35666862 http://dx.doi.org/10.1073/pnas.2122249119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Zhu, Hao Li, Meijing Zhao, Ruixue Li, Ming Chai, Yongping Zhu, Zhiwen Yang, Yihong Li, Wei Xie, Zhongyun Li, Xiaomin Lei, Kexin Li, Xueming Ou, Guangshuo In situ structure of intestinal apical surface reveals nanobristles on microvilli |
title | In situ structure of intestinal apical surface reveals nanobristles on microvilli |
title_full | In situ structure of intestinal apical surface reveals nanobristles on microvilli |
title_fullStr | In situ structure of intestinal apical surface reveals nanobristles on microvilli |
title_full_unstemmed | In situ structure of intestinal apical surface reveals nanobristles on microvilli |
title_short | In situ structure of intestinal apical surface reveals nanobristles on microvilli |
title_sort | in situ structure of intestinal apical surface reveals nanobristles on microvilli |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214534/ https://www.ncbi.nlm.nih.gov/pubmed/35666862 http://dx.doi.org/10.1073/pnas.2122249119 |
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