Vielkind Susina, Gallagher-Gambarelli Maighread, Gomez Manuel, Hinton Heather J, Cantrell Doreen A
Lymphocyte Activation Laboratory, Cancer Research U.K. London Research Institute, Lincoln's Inn Fields Laboratories, London, United Kingdom.
J Immunol. 2005 Jul 1;175(1):350-7. doi: 10.4049/jimmunol.175.1.350.
The guanine nucleotide-binding protein Rho has essential functions in T cell development and is important for the survival and proliferation of T cell progenitors in the thymus. To explore the mechanisms used by RhoA to control thymocyte biology, the role of this GTPase in the regulation of integrin-mediated cell adhesion was examined. The data show that RhoA activation is sufficient to stimulate beta(1) and beta(2) integrin-mediated adhesion in murine thymocytes. RhoA is also needed for integrin activation in vivo as loss of Rho function impaired the ability of thymocytes to adhere to the extracellular matrix protein VCAM-1 and prevented integrin activation induced by the GTPases Rac-1 and Rap1A in vivo. The regulated activity of integrins is needed for cell motility and in the present study it was seen that RhoA activity is critical for integrin-mediated thymocyte migration to chemokines in vitro. Thus, RhoA has a critical role in regulating cell adhesion and migration during T cell development.
鸟嘌呤核苷酸结合蛋白Rho在T细胞发育中具有重要功能,对胸腺中T细胞祖细胞的存活和增殖至关重要。为了探究RhoA调控胸腺细胞生物学的机制,研究了这种GTP酶在整合素介导的细胞黏附中的作用。数据表明,RhoA激活足以刺激小鼠胸腺细胞中β(1)和β(2)整合素介导的黏附。RhoA在体内整合素激活中也是必需的,因为Rho功能丧失会损害胸腺细胞黏附于细胞外基质蛋白VCAM-1的能力,并在体内阻止由GTP酶Rac-1和Rap1A诱导的整合素激活。整合素的调控活性对细胞运动是必需的,在本研究中发现,RhoA活性对于整合素介导的胸腺细胞在体外向趋化因子迁移至关重要。因此,RhoA在T细胞发育过程中对调节细胞黏附和迁移起着关键作用。