膜-皮质附着和BAR蛋白对破骨细胞融合的机械控制。

IF 7.4 1区 生物学 Q1 CELL BIOLOGY
Yumeng Wan,Yuri L Nemoto,Tsukasa Oikawa,Kazunori Takano,Takahiro K Fujiwara,Kazuya Tsujita,Toshiki Itoh
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引用次数: 0

摘要

破骨细胞是由前体细胞融合形成的多核巨细胞。细胞-细胞融合是由肌动蛋白重组驱动的膜突出介导的,但膜力学在这一过程中的作用尚不清楚。利用活细胞成像、光学镊子、操纵膜与皮层附着(MCA)和遗传干扰,我们表明,质膜(PM)张力的降低是破骨细胞融合的机械先决条件。在rankl诱导的分化过程中,融合祖细胞中ezrin的表达降低,导致mca依赖性PM张力降低。通过加强MCA强制PM张力升高反过来抑制细胞-细胞融合。从机制上讲,PM张力降低导致膜曲率诱导/传感BAR蛋白驱动的膜突侵入体形成,从而促进细胞-细胞融合。这些发现为细胞膜力学控制下细胞-细胞融合的机制提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanical control of osteoclast fusion by membrane-cortex attachment and BAR proteins.
Osteoclasts are multinucleated giant cells that are formed by the fusion of precursor cells. Cell-cell fusion is mediated by membrane protrusion driven by actin reorganization, but the role of membrane mechanics in this process is unknown. Utilizing live-cell imaging, optical tweezers, manipulation of membrane-to-cortex attachment (MCA), and genetic interference, we show that a decrease in plasma membrane (PM) tension is a mechanical prerequisite for osteoclast fusion. Upon RANKL-induced differentiation, ezrin expression in fusion progenitor cells is reduced, resulting in a decrease in MCA-dependent PM tension. A forced elevation of PM tension by reinforcing the MCA conversely suppresses cell-cell fusion. Mechanistically, reduced PM tension leads to membrane protrusive invadosome formation driven by membrane curvature-inducing/sensing BAR proteins, thereby promoting cell-cell fusion. These findings provide insights into the mechanism of cell-cell fusion under the control of membrane mechanics.
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来源期刊
Journal of Cell Biology
Journal of Cell Biology 生物-细胞生物学
CiteScore
12.60
自引率
2.60%
发文量
213
审稿时长
1 months
期刊介绍: The Journal of Cell Biology (JCB) is a comprehensive journal dedicated to publishing original discoveries across all realms of cell biology. We invite papers presenting novel cellular or molecular advancements in various domains of basic cell biology, along with applied cell biology research in diverse systems such as immunology, neurobiology, metabolism, virology, developmental biology, and plant biology. We enthusiastically welcome submissions showcasing significant findings of interest to cell biologists, irrespective of the experimental approach.
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