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巨噬细胞运动性和趋化性中的Rho GTP酶

The Rho GTPases in macrophage motility and chemotaxis.

作者信息

Jones G E, Allen W E, Ridley A J

机构信息

Muscle and Motility Research Centre, Randall Institute, King's College, London, UK.

出版信息

Cell Adhes Commun. 1998;6(2-3):237-45. doi: 10.3109/15419069809004479.

Abstract

The GTP-binding proteins, Rho, Rac and Cdc42 are known to regulate actin organisation. Rho induces the assembly of contractile actin-based microfilaments such as stress fibres, Rac regulates the formation of membrane ruffles and lamellipodia, and Cdc42 activation is necessary for the formation of filopodia. In addition, all three proteins can also regulate the assembly of integrin-containing focal adhesion complexes. The orchestration of these distinct cytoskeletal changes is thought to form the basis of the coordination of cell motility and we have investigated the roles of Rho family proteins in migration using a model system. We have found that in the macrophage cell line Bac1, the cytokine CSF-1 rapidly induces actin reorganisation: it stimulates the formation of filopodia, lamellipodia and membrane ruffles, as well as the appearance of fine actin cables within the cell. We have shown that Cdc42, Rac and Rho regulate the CSF-1 induced formation of these distinct actin filament-based structures. Using a cell tracking procedure we found that both Rho and Rac were required for CSF-1 stimulated cell translocation. In contrast, inhibition of Cdc42 does not prevent macrophages migrating in response to CSF-1, but does prevent recognition of a CSF-1 concentration gradient, so that cells now migrate randomly rather than up the gradient of this chemotactic cytokine. This implies that Cdc42, and thus probably filopodia, are required for gradient sensing and cell polarisation in macrophages.

摘要

已知GTP结合蛋白Rho、Rac和Cdc42可调节肌动蛋白的组织。Rho诱导基于肌动蛋白的收缩性微丝组装,如应力纤维;Rac调节膜皱褶和片状伪足的形成;Cdc42的激活是丝状伪足形成所必需的。此外,这三种蛋白还均可调节含整合素的粘着斑复合物的组装。这些不同的细胞骨架变化的协调作用被认为是细胞运动协调的基础,我们使用一个模型系统研究了Rho家族蛋白在细胞迁移中的作用。我们发现在巨噬细胞系Bac1中,细胞因子CSF-1可迅速诱导肌动蛋白重组:它刺激丝状伪足、片状伪足和膜皱褶的形成,以及细胞内细肌动蛋白丝的出现。我们已经证明Cdc42、Rac和Rho调节CSF-1诱导的这些不同的基于肌动蛋白丝的结构的形成。使用细胞追踪程序,我们发现Rho和Rac都是CSF-1刺激细胞转运所必需的。相比之下,抑制Cdc42并不妨碍巨噬细胞对CSF-1作出反应而迁移,但确实会妨碍对CSF-1浓度梯度的识别,因此细胞现在随机迁移而不是顺着这种趋化性细胞因子的梯度迁移。这意味着Cdc42,可能还有丝状伪足,是巨噬细胞中梯度感知和细胞极化所必需的。

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