Lou Z, Billadeau D D, Savoy D N, Schoon R A, Leibson P J
Department of Pharmacology, Mayo Graduate School, Mayo Clinic, Rochester, MN 55905, USA.
J Immunol. 2001 Nov 15;167(10):5749-57. doi: 10.4049/jimmunol.167.10.5749.
Polarization of lipid rafts and granules to the site of target contact is required for the development of cell-mediated killing by cytotoxic lymphocytes. We have previously shown that these events require the activation of proximal protein tyrosine kinases. However, the downstream intracellular signaling molecules involved in the development of cell-mediated cytotoxicity remain poorly defined. We report here that a RhoA/ROCK/LIM-kinase axis couples the receptor-initiated protein tyrosine kinase activation to the reorganization of the actin cytoskeleton required for the polarization of lipid rafts and the subsequent generation of cell-mediated cytotoxicity. Pharmacologic and genetic interruption of any element of this RhoA/ROCK/LIM-kinase pathway inhibits both the accumulation of F-actin and lipid raft polarization to the site of target contact and the subsequent delivery of the lethal hit. These data define a specialized role for a RhoA-->ROCK-->LIM-kinase pathway in cytotoxic lymphocyte activation.
细胞毒性淋巴细胞介导的细胞杀伤作用的发生需要脂筏和颗粒向靶细胞接触部位极化。我们之前已经表明,这些事件需要近端蛋白酪氨酸激酶的激活。然而,参与细胞介导的细胞毒性作用发生的下游细胞内信号分子仍不清楚。我们在此报告,RhoA/ROCK/LIM激酶轴将受体启动的蛋白酪氨酸激酶激活与脂筏极化及随后细胞介导的细胞毒性作用产生所需的肌动蛋白细胞骨架重组联系起来。该RhoA/ROCK/LIM激酶途径中任何一个元件的药理学和遗传学阻断都会抑制F-肌动蛋白的积累以及脂筏向靶细胞接触部位的极化,以及随后致命一击的传递。这些数据确定了RhoA→ROCK→LIM激酶途径在细胞毒性淋巴细胞激活中的特殊作用。