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H-Ras参与白细胞介素-3诱导的整合素激活的外向内信号通路。

H-Ras is involved in the inside-out signaling pathway of interleukin-3-induced integrin activation.

作者信息

Shibayama H, Anzai N, Braun S E, Fukuda S, Mantel C, Broxmeyer H E

机构信息

Departments of Microbiology/Immunology, Medicine, and the Walther Oncology Center, Indiana University School of Medicine, Indianapolis, IN, USA.

出版信息

Blood. 1999 Mar 1;93(5):1540-8.

Abstract

The proto-oncogene product, p21(ras), has been implicated in the cellular mechanism of adhesion, although its precise role has been controversial. Numerous cytokines and growth-factors activate Ras, which is an important component of their growth-promoting signaling pathways. On the other hand, the role of Ras in cytokine-induced adhesion has not been elucidated. We therefore investigated the function of H-Ras in the inside-out signaling pathway of interleukin-3 (IL-3)-induced integrin activation in the murine Baf3 cell line after transfection of cells with either constitutively active, dominant-negative, or wild-type H-Ras cDNAs. Adhesion of Baf3 cells to fibronectin was induced by IL-3 in a dose-dependent manner via very late antigen-4 (VLA-4; alpha4beta1 integrins) and VLA-5 (alpha5beta1 integrins) activation. On the other hand, IL-4 did not induce the adhesion of Baf3 cells to fibronectin, although IL-4 did stimulate the cell proliferation of Baf3 cells. Constitutively active H-Ras-transfected Baf3 cells adhered to fibronectin without IL-3 stimulation through VLA-4 and VLA-5, whereas dominant-negative H-Ras-transfected Baf3 cells showed significantly less adhesion induced by IL-3 compared with wild-type and constitutively active H-Ras-transfected Baf3 cells. Anti-beta1 integrin antibody (clone; 9EG7), which is known to change integrin conformation and activate integrins, induced the adhesion of dominant-negative H-Ras-transfected Baf3 cells as much as the other types of H-Ras-transfected Baf3 cells. 8-Br-cAMP, Dibutyryl-cAMP, Ras-Raf-1 pathway inhibitors, and PD98059, a MAPK kinase inhibitor, suppressed proliferation and phosphorylation of MAPK detected by Western blotting with anti-phospho-MAPK antibody, but not adhesion of any type of H-Ras-transfected Baf3 cells, whereas U-73122, a phospholipase C (PLC) inhibitor, suppressed adhesion of these cells completely. These data indicate that H-Ras and PLC, but not Raf-1, MAPK kinase, or the MAPK pathway, are involved in the inside-out signaling pathway of IL-3-induced VLA-4 and VLA-5 activation in Baf3 cells.

摘要

原癌基因产物p21(ras)已被认为参与细胞黏附机制,但其确切作用一直存在争议。许多细胞因子和生长因子可激活Ras,而Ras是它们促进生长信号通路的重要组成部分。另一方面,Ras在细胞因子诱导的黏附中的作用尚未阐明。因此,在用组成型活性、显性负性或野生型H-Ras cDNA转染小鼠Baf3细胞系后,我们研究了H-Ras在白细胞介素-3(IL-3)诱导的整联蛋白激活的外向内信号通路中的功能。IL-3通过极迟抗原-4(VLA-4;α4β1整联蛋白)和VLA-5(α5β1整联蛋白)激活以剂量依赖方式诱导Baf3细胞与纤连蛋白黏附。另一方面,IL-4虽然能刺激Baf3细胞增殖,但不诱导Baf3细胞与纤连蛋白黏附。组成型活性H-Ras转染的Baf3细胞在无IL-3刺激的情况下通过VLA-4和VLA-5与纤连蛋白黏附,而显性负性H-Ras转染的Baf3细胞与野生型和组成型活性H-Ras转染的Baf3细胞相比,IL-3诱导的黏附明显减少。已知可改变整联蛋白构象并激活整联蛋白的抗β1整联蛋白抗体(克隆;9EG7)诱导显性负性H-Ras转染的Baf3细胞黏附的程度与其他类型的H-Ras转染的Baf3细胞相同。8-溴-cAMP、二丁酰-cAMP、Ras-Raf-1通路抑制剂和MAPK激酶抑制剂PD98059可抑制用抗磷酸化-MAPK抗体进行蛋白质印迹检测到的MAPK的增殖和磷酸化,但不抑制任何类型的H-Ras转染的Baf3细胞的黏附,而磷脂酶C(PLC)抑制剂U-73122可完全抑制这些细胞的黏附。这些数据表明,H-Ras和PLC而非Raf-1、MAPK激酶或MAPK通路参与了IL-3诱导的Baf3细胞中VLA-4和VLA-5激活的外向内信号通路。

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