T细胞受体
CD3型
T细胞
细胞生物学
细胞内
生物
分子生物学
化学
CD8型
抗原
免疫学
免疫系统
作者
Hiroshi Ohno,Chifuyu Ushiyama,M Taniguchi,R N Germain,Takashi Saito
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:1991-06-01
卷期号:146 (11): 3742-3746
被引量:40
标识
DOI:10.4049/jimmunol.146.11.3742
摘要
T lymphocytes can be activated clonotypically through TCR/CD3 complex or polyclonally via the CD2 molecule. Whether CD2-mediated activation is dependent on TCR/CD3 expression or signaling is controversial. We have re-explored this issue by using a series of CD2-transfected, TCR/CD3 surface membrane-negative human and mouse T cells. Our results clearly show that such T cells can be triggered for IL-2 secretion and increases in intracellular Ca2+ through the CD2 molecule in the absence of surface expression of TCR/CD3 complexes. These responses are only observed when cells express high levels of CD2 and there is a critical threshold of CD2 expression necessary for such activation in the absence of CD3. Concomitant expression of TCR/CD3 complex markedly lowers the level of CD2 required for activation via the latter pathway. These results provide a clear resolution of the controversy concerning the requirement for surface CD3 expression in T cell activation through CD2 and further suggest a possible role for CD2 in activation of TCR/CD3-negative cells.
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