Transmembrane signaling via both CD3 and CD2 human T cell surface molecules involves protein kinase-C translocation.

M Bagnasco, J Nunes, M Lopez, C Lipcey, C Mawas, D Olive
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引用次数: 5

Abstract

The activation of T lymphocytes by appropriate pairs of anti-CD2 monoclonal antibodies has been shown to involve phospholipase-C and phosphoinositide hydrolysis. In this paper we show that the stimulation of the human cloned leukemic T cell line Jurkat by anti-CD2 as well as anti-CD3 monoclonal antibodies induces translocation from cytosol to cell membrane of protein kinase-C (PKC), which is dependent on the formation of 1,2-diacylglycerol from inositol 4,5-diphosphate. PKC translocation is rapid and transient: the kinetics of enzyme redistribution are similar for CD2 and CD3. These results further stress that CD2 and CD3 T cell activation pathways use similar signal transducing mechanisms.

通过CD3和CD2人T细胞表面分子的跨膜信号传导涉及蛋白激酶- c易位。
适当的抗cd2单克隆抗体对T淋巴细胞的激活已被证明涉及磷脂酶- c和磷酸肌肽水解。在本文中,我们证明了用抗cd2和抗cd3单克隆抗体刺激人克隆白血病T细胞系Jurkat诱导蛋白激酶c (PKC)从细胞质转移到细胞膜,这依赖于由4,5-二磷酸肌醇形成1,2-二酰基甘油。PKC易位是快速而短暂的:CD2和CD3的酶重分配动力学相似。这些结果进一步强调CD2和CD3 T细胞激活途径使用相似的信号转导机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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