Prabhu Das M R, Zamvil S S, Borriello F, Weiner H L, Sharpe A H, Kuchroo V K
Center for Neurologic Diseases, Brigham and Women's Hospital, Boston, MA 02115.
Eur J Immunol. 1995 Jan;25(1):207-11. doi: 10.1002/eji.1830250134.
The co-stimulatory B7 molecules (B7-1 and B7-2) are expressed on professional antigen-presenting cells in mice. In this study, we demonstrate that B7-1 (CD80) and B7-2 (CD86) are also expressed on murine T cells in the absence of major histocompatibility complex class II molecules. The temporal expression of these two molecules on T cells varies with the state of activation where resting T cells express B7-2 but show little or no expression of B7-1. Following activation, B7-2 expression is down-regulated and there is a concomitant increase in the expression of B7-1 on the cell surface which peaks at about 72 h. Thus these two co-stimulatory molecules are reciprocally expressed on the T cell surface. This pattern of expression of B7-1 and B7-2 on T cells suggests that these two molecules may have different roles in the generation and regulation of immune responses.
共刺激分子B7(B7-1和B7-2)在小鼠的专职抗原呈递细胞上表达。在本研究中,我们证明在缺乏主要组织相容性复合体II类分子的情况下,B7-1(CD80)和B7-2(CD86)也在鼠T细胞上表达。这两种分子在T细胞上的瞬时表达随激活状态而变化,静息T细胞表达B7-2,但几乎不表达或不表达B7-1。激活后,B7-2表达下调,细胞表面B7-1的表达随之增加,在约72小时达到峰值。因此,这两种共刺激分子在T细胞表面呈相互表达。B7-1和B7-2在T细胞上的这种表达模式表明,这两种分子在免疫反应的产生和调节中可能具有不同作用。