Li M, Yang J, Shen G X, Zhang Q, Liu S P, Liu Z B, Ye W X
Department of Immunology, Tongji Medical University, Wuhan.
J Tongji Med Univ. 1994;14(4):209-12. doi: 10.1007/BF02897669.
T cell activation and proliferation via CD3-TCR complex were investigated by lymphocyte DNA synthesis in vitro. Several interfering factors were also discussed. The result indicated that lymphocyte activation and proliferation are calcium-dependent. A rise of cytoplasmic free Ca2+ quickly following activation with CD3 McAb is mainly due to intracellular mobilization of Ca2+, while lymphocyte proliferation needs both intracellular mobilization of Ca2+ as well as influx of extracellular Ca2+. It was confirmed that CTX sensitive G protein plays a role in regulating T cell proliferation by pretreatment with CTX suppressing lymphocyte H-TdR incorporation obviously. PLC and PKC inhibitor neomycin and P. S. S could also decrease T cell proliferation.
通过体外淋巴细胞DNA合成研究了经由CD3-TCR复合物的T细胞活化和增殖。还讨论了几种干扰因素。结果表明,淋巴细胞活化和增殖是钙依赖性的。用CD3单克隆抗体激活后,细胞质游离Ca2+迅速升高,这主要是由于细胞内Ca2+的动员,而淋巴细胞增殖既需要细胞内Ca2+的动员,也需要细胞外Ca2+的流入。通过用CTX预处理明显抑制淋巴细胞H-TdR掺入,证实了CTX敏感的G蛋白在调节T细胞增殖中起作用。PLC和PKC抑制剂新霉素和P.S.S也可降低T细胞增殖。