Asymmetric branched F-actin networks at apical clathrin coated pits support microvillar biogenesis.

IF 2.7 3区 生物学 Q3 CELL BIOLOGY
Molecular Biology of the Cell Pub Date : 2026-06-01 Epub Date: 2026-04-08 DOI:10.1091/mbc.E25-12-0606
Olivia L Perkins, Malcom Díaz García, Matthew J Tyska
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引用次数: 0

Abstract

Microvilli are conserved actin-based protrusions that expand surface area and absorptive capacity in epithelial tissues. In humans, the intestinal tract grows 300 trillion microvilli per day, yet the molecular mechanisms defining where and when microvilli grow remain unclear. Using a combination of live-cell confocal and super-resolution microscopy to investigate native intestinal tissues and epithelial cell culture models, we found that microvilli grow from Arp2/3-generated branched actin networks that form on the surface of clathrin-coated pits. These transient networks are stabilized by cortactin and localize to the apical plasma membrane minutes before reorganizing into the linear core actin bundles that support microvilli. Moreover, subpixel precision localization of coated pit and microvilli markers revealed that F-actin asymmetrically localizes to one side of a nascent clathrin-coated pit, and that microvilli grow from the side with the highest F-actin density. These findings support a model where the asymmetric accumulation of F-actin and growing barbed ends on the surface of a clathrin-coated pit offers a filament source to support microvilli formation.

不对称分支的f -肌动蛋白网络支持微绒毛的生物发生。
微绒毛是保守的基于肌动蛋白的突起,在上皮组织中扩大表面积和吸收能力。在人类中,肠道每天生长300万亿个微绒毛,然而决定微绒毛何时何地生长的分子机制尚不清楚。通过结合活细胞共聚焦和超分辨率N-SPARC显微镜研究天然肠道组织和上皮细胞培养模型,我们发现微绒毛是由arp2 /3生成的分支肌动蛋白网络生长的,这些网络形成于网格蛋白包覆的凹坑表面。这些瞬时网络通过接触稳定下来,并在重组成支持微绒毛的线状核心肌动蛋白束之前几分钟定位于顶端质膜。此外,对包被坑和微绒毛标记物的亚像素精确定位表明,f -肌动蛋白不对称地定位于新生网格蛋白包被坑的一侧,微绒毛从f -肌动蛋白密度最高的一侧生长。这些发现支持了一个模型,即f -肌动蛋白的不对称积累和网格蛋白包覆坑表面上不断生长的倒钩端提供了支持微绒毛形成的丝源。[媒体:见文本]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Biology of the Cell
Molecular Biology of the Cell 生物-细胞生物学
CiteScore
6.00
自引率
6.10%
发文量
402
审稿时长
2 months
期刊介绍: MBoC publishes research articles that present conceptual advances of broad interest and significance within all areas of cell, molecular, and developmental biology. We welcome manuscripts that describe advances with applications across topics including but not limited to: cell growth and division; nuclear and cytoskeletal processes; membrane trafficking and autophagy; organelle biology; quantitative cell biology; physical cell biology and mechanobiology; cell signaling; stem cell biology and development; cancer biology; cellular immunology and microbial pathogenesis; cellular neurobiology; prokaryotic cell biology; and cell biology of disease.
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