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DAAM 介导在集体迁移的上皮细胞中长寿命、 treadmilling 应激纤维的组装。

DAAM mediates the assembly of long-lived, treadmilling stress fibers in collectively migrating epithelial cells in .

机构信息

Department of Molecular Genetics and Cell Biology, The University of Chicago, Chicago, United States.

Committee on Development, Regeneration, and Stem Cell Biology, The University of Chicago, Chicago, United States.

出版信息

Elife. 2021 Nov 23;10:e72881. doi: 10.7554/eLife.72881.

DOI:10.7554/eLife.72881
PMID:34812144
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8610420/
Abstract

Stress fibers (SFs) are actomyosin bundles commonly found in individually migrating cells in culture. However, whether and how cells use SFs to migrate in vivo or collectively is largely unknown. Studying the collective migration of the follicular epithelial cells in , we found that the SFs in these cells show a novel treadmilling behavior that allows them to persist as the cells migrate over multiple cell lengths. Treadmilling SFs grow at their fronts by adding new integrin-based adhesions and actomyosin segments over time. This causes the SFs to have many internal adhesions along their lengths, instead of adhesions only at the ends. The front-forming adhesions remain stationary relative to the substrate and typically disassemble as the cell rear approaches. By contrast, a different type of adhesion forms at the SF's terminus that slides with the cell's trailing edge as the actomyosin ahead of it shortens. We further show that SF treadmilling depends on cell movement and identify a developmental switch in the formins that mediate SF assembly, with Dishevelled-associated activator of morphogenesis acting during migratory stages and Diaphanous acting during postmigratory stages. We propose that treadmilling SFs keep each cell on a linear trajectory, thereby promoting the collective motility required for epithelial migration.

摘要

应力纤维(SFs)是普遍存在于培养的单个迁移细胞中的肌动球蛋白束。然而,细胞是否以及如何在体内使用 SFs 进行迁移,在很大程度上是未知的。在研究卵泡上皮细胞的集体迁移时,我们发现这些细胞中的 SFs 表现出一种新颖的履带式行为,使它们能够在多个细胞长度上迁移时保持存在。履带式 SFs 通过随着时间的推移在新的整合素基附着和肌动球蛋白段上生长来在其前缘生长。这导致 SF 沿着它们的长度具有许多内部附着,而不是仅在末端有附着。相对于基底,形成前缘的附着保持静止,并且通常在细胞后缘接近时解体。相比之下,在 SF 的末端形成另一种类型的附着,当位于其前方的肌动球蛋白缩短时,该附着与细胞的后缘一起滑动。我们进一步表明,SF 履带式运动取决于细胞运动,并确定了介导 SF 组装的formin 的发育开关,其中 Dishevelled 相关形态发生激活蛋白在迁移阶段起作用,而 Diaphanous 在迁移后阶段起作用。我们提出,履带式 SF 使每个细胞保持在线性轨迹上,从而促进上皮细胞迁移所需的集体运动。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/8610420/f2d846d04208/elife-72881-sa2-fig1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/8610420/f2d846d04208/elife-72881-sa2-fig1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/8610420/db4a0b92c1d8/elife-72881-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/8610420/47b4034bcd9e/elife-72881-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/8610420/2a369d6908fc/elife-72881-fig2-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/8610420/3d3b95d63356/elife-72881-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/8610420/d5e74a1dab21/elife-72881-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/8610420/88a9c47d3fee/elife-72881-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/8610420/31727d065661/elife-72881-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/8610420/41f3332156f9/elife-72881-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/8610420/d8ea094a888b/elife-72881-fig6-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/8610420/9ab956b01267/elife-72881-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/8610420/6278b9f8a32f/elife-72881-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aadf/8610420/f2d846d04208/elife-72881-sa2-fig1.jpg

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