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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
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.
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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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