Crabtree G R
Department of Pathology, Stanford University Medical School, CA.
Science. 1989 Jan 20;243(4889):355-61. doi: 10.1126/science.2783497.
Interaction of antigen in the proper histocompatibility context with the T lymphocyte antigen receptor leads to an orderly series of events resulting in morphologic change, proliferation, and the acquisition of immunologic function. In most T lymphocytes two signals are required to initiate this process, one supplied by the antigen receptor and the other by accessory cells or agents that activate protein kinase C. Recently, DNA sequences have been identified that act as response elements for one or the other of the two signals, but do not respond to both signals. The fact that these sequences lie within the control regions of the same genes suggests that signals originating from separate cell membrane receptors are integrated at the level of the responsive gene. The view is put forth that these signals initiate a contingent series of gene activations that bring about proliferation and impart immunologic function.
在适当的组织相容性背景下,抗原与T淋巴细胞抗原受体相互作用会引发一系列有序的事件,导致形态变化、增殖以及免疫功能的获得。在大多数T淋巴细胞中,启动这一过程需要两个信号,一个由抗原受体提供,另一个由激活蛋白激酶C的辅助细胞或因子提供。最近,已鉴定出一些DNA序列,它们作为这两个信号中某一个的反应元件,但对两个信号都无反应。这些序列位于相同基因的调控区域内,这一事实表明源自不同细胞膜受体的信号在反应基因水平上整合。有人提出这些信号引发一系列偶然的基因激活,从而导致增殖并赋予免疫功能。