Granulysin: killer lymphocyte safeguard against microbes

被引:40
|
作者
Dotiwalal, Farokh [1 ]
Lieberman, Judy [2 ,3 ]
机构
[1] Wistar Inst Anat & Biol, Vaccine & Immunotherapy Ctr, Philadelphia, PA 19104 USA
[2] Harvard Med Sch, Program Cellular & Mol Med, Boston Childrens Hosp, Boston, MA 02115 USA
[3] Harvard Med Sch, Dept Pediat, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
STEVENS-JOHNSON SYNDROME; CD8(+) T-CELLS; GRANZYME-B; MYCOBACTERIUM-TUBERCULOSIS; NK CELLS; CRYPTOCOCCUS-NEOFORMANS; ANTIMICROBIAL ACTIVITY; PLASMODIUM-FALCIPARUM; SERUM GRANULYSIN; PERFORIN;
D O I
10.1016/j.coi.2019.04.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Primary T cell immunodeficiency and HIV-infected patients are plagued by non-viral infections caused by bacteria, fungi, and parasites, suggesting an important and underappreciated role for T lymphocytes in controlling microbes. Here, we review recent studies showing that killer lymphocytes use the antimicrobial cytotoxic granule pore-forming peptide granulysin, induced by microbial exposure, to permeabilize cholesterol-poor microbial membranes and deliver death inducing granzymes into these pathogens. Granulysin and granzymes cause microptosis, programmed cell death in microbes, by inducing reactive oxygen species and destroying microbial antioxidant defenses and disrupting biosynthetic and central metabolism pathways required for their survival, including protein synthesis, glycolysis, and the Krebs cycle.
引用
收藏
页码:19 / 29
页数:11
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