细胞毒性T细胞
淋巴细胞性脉络膜脑膜炎
颗粒酶B
生物
颗粒酶
细胞凋亡
颗粒酶A
弹力素
免疫学
病毒学
穿孔素
生物化学
体外
作者
Manling Zhang,Sun Mi Park,Yue Wang,Ramila Shah,Lei Ni,Andrea E. Murmann,Chyung Ru Wang,Peter Marynen,Philip G. Ashton‐Rickardt
出处
期刊:Immunity
[Elsevier]
日期:2006-04-01
卷期号:24 (4): 451-461
被引量:112
标识
DOI:10.1016/j.immuni.2006.02.002
摘要
How cytotoxic T lymphocytes (CTLs) kill intracellular pathogens without killing themselves has been a recurring question ever since their discovery. By using mice deficient in Serine Protease Inhibitor 6 (Spi6), we show that by inhibiting granzyme B (GrB), Spi6 protects CTLs from self-inflicted injury. Infection with either Lymphocytic Choriomeningitis virus (LCMV) or Listeria monocytogenes (LM) revealed increased apoptosis and diminished survival of Spi6 knockout (KO) CTLs, which was cell autonomous and could be corrected by GrB deficiency. Spi6 KO mice in turn were impaired in their ability to clear LCMV infection. Spi6 KO CTLs revealed a breakdown in the integrity of cytotoxic granules, increased cytoplasmic GrB, and ensuing apoptosis. We conclude that Spi6 protects CTLs from suicide caused by GrB-mediated breakdown of cytotoxic granules.
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