Phatak P D, Packman C H, Lichtman M A
Department of Medicine, University of Rochester School of Medicine and Dentistry, NY 14642.
J Immunol. 1988 Nov 1;141(9):2929-34.
We studied the effect of activators and inhibitors of protein kinase C on actin conformation in human blood lymphocytes by flow cytometry and gel electrophoresis. PMA, 1-oleyl-2-acetyl-glycerol, and mezerein, activators of protein kinase C, caused an increase in lymphocyte F-actin within 2 to 5 min. After stimulation with PMA, lymphocytes formed pseudopods containing an increased concentration of F-actin and had an increase of actin in the Triton-insoluble cytoskeletal fraction. Sphingosine and H-7, inhibitors of protein kinase C activation, inhibited the increase in F-actin induced by PMA. The increase in F-actin in response to PMA was striking in Th and Ts lymphocytes (2- to 3-fold increase), but B lymphocytes had only a slight increase (1.15-fold). Thus, activation of protein kinase C modulates actin conformation specifically in T lymphocytes.
我们通过流式细胞术和凝胶电泳研究了蛋白激酶C激活剂和抑制剂对人血淋巴细胞中肌动蛋白构象的影响。蛋白激酶C激活剂佛波酯(PMA)、1-油酰基-2-乙酰甘油和瑞香毒素,在2至5分钟内导致淋巴细胞F-肌动蛋白增加。用PMA刺激后,淋巴细胞形成含有浓度增加的F-肌动蛋白的伪足,并且在不溶于曲拉通的细胞骨架部分中肌动蛋白增加。鞘氨醇和H-7,蛋白激酶C激活的抑制剂,抑制了PMA诱导的F-肌动蛋白增加。在Th和Ts淋巴细胞中,对PMA反应的F-肌动蛋白增加显著(增加2至3倍),但B淋巴细胞只有轻微增加(1.15倍)。因此,蛋白激酶C的激活特异性地调节T淋巴细胞中的肌动蛋白构象。