肌球蛋白 II 张力传感器可视化活细胞中肌动蛋白细胞骨架内产生的力。

IF 3.3 3区 生物学 Q3 CELL BIOLOGY
Journal of cell science Pub Date : 2024-10-15 Epub Date: 2024-10-30 DOI:10.1242/jcs.262281
Ryan G Hart, Divya Kota, Fangjia Li, Mengdi Zhang, Diego Ramallo, Andrew J Price, Karla L Otterpohl, Steve J Smith, Alexander R Dunn, Mark O Huising, Jing Liu, Indra Chandrasekar
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引用次数: 0

摘要

非肌肉肌球蛋白 II 产生的细胞骨架力驱动着细胞分裂、胚胎发育、肌肉收缩和许多其他细胞功能。然而,目前还没有一种方法可以直接测量肌球蛋白在活细胞中产生的作用力。在这里,我们描述了一种基于佛斯特共振能量转移(FRET)的张力传感器,它可以沿着丝状肌动蛋白网络检测肌球蛋白相关的力。荧光寿命成像显微镜(FLIM)-FRET 测量结果表明,NMIIB 产生的力与供体寿命和荧光团能量交换有关,表现出显著的空间和时间异质性。这些测量结果为沿肌动蛋白细胞骨架广泛变化的推断力提供了替代物。这份初步报告强调了基于肌球蛋白的张力传感器在阐明细胞骨架收缩性在各种情况下的作用方面的潜在用途。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Myosin II tension sensors visualize force generation within the actin cytoskeleton in living cells.

Nonmuscle myosin II (NMII) generates cytoskeletal forces that drive cell division, embryogenesis, muscle contraction and many other cellular functions. However, at present there is no method that can directly measure the forces generated by myosins in living cells. Here, we describe a Förster resonance energy transfer (FRET)-based tension sensor that can detect myosin-associated force along the filamentous actin network. Fluorescence lifetime imaging microscopy (FLIM)-FRET measurements indicate that the forces generated by NMII isoform B (NMIIB) exhibit significant spatial and temporal heterogeneity as a function of donor lifetime and fluorophore energy exchange. These measurements provide a proxy for inferred forces that vary widely along the actin cytoskeleton. This initial report highlights the potential utility of myosin-based tension sensors in elucidating the roles of cytoskeletal contractility in a wide variety of contexts.

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来源期刊
Journal of cell science
Journal of cell science 生物-细胞生物学
CiteScore
7.30
自引率
2.50%
发文量
393
审稿时长
1.4 months
期刊介绍: Journal of Cell Science publishes cutting-edge science, encompassing all aspects of cell biology.
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