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白细胞中膜皱褶形成和吞噬作用对Rac1和Cdc42的需求。

Requirements for both Rac1 and Cdc42 in membrane ruffling and phagocytosis in leukocytes.

作者信息

Cox D, Chang P, Zhang Q, Reddy P G, Bokoch G M, Greenberg S

机构信息

Pulmonary Division, Department of Medicine, Columbia University College of Physicians and Surgeons, New York 10032, USA.

出版信息

J Exp Med. 1997 Nov 3;186(9):1487-94. doi: 10.1084/jem.186.9.1487.

Abstract

Specific pathways linking heterotrimeric G proteins and Fcgamma receptors to the actin-based cytoskeleton are poorly understood. To test a requirement for Rho family members in cytoskeletal events mediated by structurally diverse receptors in leukocytes, we transfected the full-length human chemotactic peptide receptor in RAW 264.7 cells and examined cytoskeletal alterations in response to the chemotactic peptide formyl-methionyl-leucyl-phenylalanine (FMLP), colony stimulating factor-1 (CSF-1), IgG-coated particles, and phorbol 12-myristate 13-acetate (PMA). Expression of Rac1 N17, Cdc42 N17, or the GAP domain of n-chimaerin inhibited cytoskeletal responses to FMLP and CSF-1, and blocked phagocytosis. Accumulation of F-actin- rich "phagocytic cups" was partially inhibited by expression of Rac1 N17 or Cdc42 N17. In contrast, PMA-induced ruffling was not inhibited by expression of Rac1 N17, but was blocked by expression of Cdc42 N17, indicating that cytoskeletal inhibition by these constructs was nonoverlapping. These results demonstrate differential requirements for Rho family GTPases in leukocyte motility, and indicate that both Rac1 and Cdc42 are required for Fcgamma receptor- mediated phagocytosis and for membrane ruffling mediated by structurally distinct receptors in macrophages.

摘要

连接异源三聚体G蛋白和Fcγ受体至基于肌动蛋白的细胞骨架的特定信号通路仍知之甚少。为了检测Rho家族成员在白细胞中由结构多样的受体介导的细胞骨架事件中的需求,我们将全长人趋化肽受体转染至RAW 264.7细胞中,并检测了细胞对趋化肽甲酰甲硫氨酰亮氨酰苯丙氨酸(FMLP)、集落刺激因子-1(CSF-1)、IgG包被颗粒及佛波酯12-肉豆蔻酸13-乙酸酯(PMA)的细胞骨架改变。Rac1 N17、Cdc42 N17或n-嵌合蛋白的GAP结构域的表达抑制了细胞对FMLP和CSF-1的细胞骨架反应,并阻断了吞噬作用。富含F-肌动蛋白的“吞噬杯”的积累被Rac1 N17或Cdc42 N17的表达部分抑制。相反,PMA诱导的边缘波动未被Rac1 N17的表达抑制,但被Cdc42 N17的表达阻断,表明这些构建体对细胞骨架的抑制作用不重叠。这些结果证明了Rho家族GTP酶在白细胞运动中的不同需求,并表明Rac1和Cdc42均是Fcγ受体介导的吞噬作用以及巨噬细胞中由结构不同的受体介导的膜边缘波动所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccc9/2199122/43f8ef7b6d8d/JEM.971092f1a.jpg

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