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足突环产生驱动破骨细胞跳跃式迁移的力。

Podosome rings generate forces that drive saltatory osteoclast migration.

机构信息

Laboratoire de Physique, UMR 5672, Lyon 69364, France.

出版信息

Mol Biol Cell. 2011 Sep;22(17):3120-6. doi: 10.1091/mbc.E11-01-0086. Epub 2011 Jul 7.

Abstract

Podosomes are dynamic, actin-containing adhesion structures that collectively self-organize as rings. In this study, we first show by observing osteoclasts plated on bead-seeded soft substrates that podosome assemblies, such as rings, are involved in tension forces. During the expansion of a podosome ring, substrate displacement is oriented outward, suggesting that podosomal structures push the substrate away. To further elucidate the function of forces generated by podosomes, we analyze osteoclast migration. Determining the centers of mass of the whole cell (G) and of actin (P), we demonstrate that osteoclasts migrate by "jumps" and that the trajectories of G and P are strongly correlated. The velocity of the center of mass as a function of time reveals that osteoclasts rapidly catch up with podosomal structures in a periodic pattern. We conclude that actin dynamics inside the cell are not only correlated with cell migration, but drive it.

摘要

Podosomes 是含有肌动蛋白的动态黏附结构,它们会集体自组织成环状。在这项研究中,我们首先通过观察在珠粒接种的软基质上培养的破骨细胞,发现 podosome 组装体(如环)参与张力。在 podosome 环的扩展过程中,基质位移向外,表明 podosomal 结构将基质推开。为了进一步阐明 podosomes 产生的力的功能,我们分析了破骨细胞的迁移。确定整个细胞(G)和肌动蛋白(P)的质心,我们证明破骨细胞通过“跳跃”进行迁移,并且 G 和 P 的轨迹高度相关。质心随时间的速度揭示了破骨细胞以周期性模式快速追上 podosome 结构。我们得出结论,细胞内的肌动蛋白动力学不仅与细胞迁移相关,而且驱动迁移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad34/3164459/6c9a86b7075a/3120fig1.jpg

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