膜序调节网格蛋白包覆坑动力学,但不调节起始。

IF 2.7 3区 生物学 Q3 CELL BIOLOGY
Molecular Biology of the Cell Pub Date : 2025-07-01 Epub Date: 2025-04-30 DOI:10.1091/mbc.E25-02-0081
G Aditya Kumar, Yousef Bagheri, Manojkumar A Puthenveedu
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引用次数: 0

摘要

网格蛋白介导的内吞作用包括通过网格蛋白包覆的小坑(ccp)的起始、成熟和断裂来重塑膜。如何调控CCP的起始和动力学主要是从介导内吞作用的核心蛋白的角度来解决的。膜的物理性质是否以及如何调节CCP的发生和动力学还没有得到充分的研究。在这里,我们使用溶剂致变色探针,在全内反射荧光显微镜下,读取正在内吞作用的活细胞的质膜中的膜顺序。胆固醇消耗降低了膜秩序,减少了CCP的发生,增加了CCP的寿命。然而,在未受干扰的细胞中,膜顺序与CCP寿命相关,而与它们的起始无关。在不提取脂质的情况下,单独降低或增加膜阶,影响CCP寿命,但不影响CCP起始。总之,通过读出活细胞内吞过程中的膜顺序和在两个方向上操纵膜顺序,我们表明膜顺序主要调节CCP动力学,胆固醇提取对CCP起始具有独立于其顺序的额外影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Membrane order regulates clathrin-coated pit dynamics but not initiation.

Clathrin-mediated endocytosis involves the remodeling of membranes via the initiation, maturation, and scission of clathrin-coated pits (CCPs). How CCP initiation and dynamics are regulated has been addressed primarily from the perspective of the core proteins that mediate endocytosis. Whether and how the physical properties of the membrane regulate CCP initiation and dynamics are heavily underexplored. Here, we used a solvatochromic probe to readout membrane order in the plasma membrane in live cells undergoing endocytosis, using total internal reflection fluorescence microscopy. Cholesterol depletion decreased membrane order, and reduced CCP initiation and increased lifetimes of CCPs. In unperturbed cells, however, membrane order was correlated to CCP lifetimes, but not their initiation. When membrane order was decreased or increased independently without extracting lipids, CCP lifetimes were affected, but CCP initiation was not. Together, by reading out membrane order in living cells undergoing endocytosis and manipulating membrane order in both directions, we show that membrane order primarily regulates CCP dynamics, and that cholesterol extraction has additional effects on CCP initiation independent of its effect on order.

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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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