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Rho GTP酶、WAS蛋白与分化对人树突状细胞细胞骨架的构型作用

Configuration of human dendritic cell cytoskeleton by Rho GTPases, the WAS protein, and differentiation.

作者信息

Burns S, Thrasher A J, Blundell M P, Machesky L, Jones G E

机构信息

Molecular Immunology Unit, Institute of Child Health, University College London, United Kingdom.

出版信息

Blood. 2001 Aug 15;98(4):1142-9. doi: 10.1182/blood.v98.4.1142.

Abstract

The cellular mechanisms that configure the cytoskeleton during migration of dendritic cells (DCs) are poorly understood. Immature DCs assemble specialized adhesion structures known as podosomes at their leading edge; these are associated with the localized recruitment of the Wiskott-Aldrich Syndrome protein (WASp) and the actin organizing actin-related protein 2/3 complex. In immature DCs lacking WASp, podosomes are absent, residual dysmorphic lamellipodia and filopodia are nonpolarized, and migration is severely compromised. Microinjection studies indicate that podosome assembly and polarization require concerted action of Cdc42, Rac, and Rho, thereby providing a link between sequential protrusive and adhesive activity. Formation of podosomes is restricted to cells with an immature phenotype, indicating a specific role for these structures during the early migratory phase. (Blood. 2001;98:1142-1149)

摘要

在树突状细胞(DC)迁移过程中构建细胞骨架的细胞机制目前尚不清楚。未成熟的DC在其前沿组装称为足体的特殊粘附结构;这些结构与威斯科特-奥尔德里奇综合征蛋白(WASp)的局部募集以及肌动蛋白组织肌动蛋白相关蛋白2/3复合物有关。在缺乏WASp的未成熟DC中,足体不存在,残留的畸形片状伪足和丝状伪足是非极化的,迁移受到严重损害。显微注射研究表明,足体组装和极化需要Cdc42、Rac和Rho的协同作用,从而在连续的突出和粘附活动之间建立联系。足体的形成仅限于具有未成熟表型的细胞,表明这些结构在早期迁移阶段具有特定作用。(《血液》。2001年;98:1142 - 1149)

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