细胞毒性T细胞
颗粒酶
颗粒酶B
生物
白细胞介素21
细胞凋亡
自然杀伤性T细胞
免疫系统
淋巴因子激活杀伤细胞
雌激素
癌症研究
T细胞
免疫学
内分泌学
穿孔素
CD8型
生物化学
体外
作者
Xinguo Jiang,Brent A. Orr,David M. Kranz,David J. Shapiro
出处
期刊:Endocrinology
[The Endocrine Society]
日期:2005-11-24
卷期号:147 (3): 1419-1426
被引量:70
摘要
Exposure to estrogens is associated with an increased risk of developing breast, cervical, and liver cancer. Estrogens strongly induce the human granzyme B inhibitor, proteinase inhibitor 9 (PI-9). Because cytotoxic T lymphocytes (CTLs) and natural killer (NK) cells use the granzyme pathway to induce apoptosis of target cells, we tested the ability of activated CTLs and the human NK cell line, YT cells, to lyse human liver cells. Estrogen induction of PI-9 protected the liver cells against CTL and NK cell-mediated, granzyme-dependent, apoptosis. Knockdown of PI-9 by RNA interference blocked the protective effect of estrogen. This work demonstrates that estrogens can act on target cells to control their destruction by immune system cells and shows that induction of PI-9 expression can inhibit both CTL and NK cell-mediated apoptosis. Estrogen induction of PI-9 may reduce the ability of cytolytic lymphocytes-mediated immune surveillance to destroy newly transformed cells, possibly providing a novel mechanism for an estrogen-mediated increase in tumor incidence.
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