Cutting Edge: Chromatin Accessibility Programs CD8 T Cell Memory

被引:61
作者
Scharer, Christopher D.
Bally, Alexander P. R.
Gandham, Bhanu
Boss, Jeremy M.
机构
[1] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Emory Vaccine Ctr, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
TRANSCRIPTION FACTORS; VIRAL PERSISTENCE; EXHAUSTION; INFECTION; VIRUS; NAIVE; DIFFERENTIATION; ANTIGEN; PD-1; DEMETHYLATION;
D O I
10.4049/jimmunol.1602086
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD8 T cell memory is characterized by rapid recall of effector function, increased proliferation, and reduced activation requirements. Despite the extensive functional characterization, the molecular mechanisms that facilitate these enhanced properties are not well characterized. In this study, the assay for transposase-accessible chromatin sequencing was employed to map the cis-regulatory elements in CD8 T cells responding to acute and chronic lymphocytic choriomeningitis virus infections. Integration of chromatin accessibility profiles with gene expression data identified unique regulatory modules that were enriched for distinct combinations of transcription factor-binding motifs. Memory CD8 T cells displayed a chromatin accessibility structure that was absent from other acute and exhausted cells types and included key effector and proliferative genes. Stimulation of memory cells revealed enhanced transcription of "memory-primed" genes compared with naive cells. Thus, memory CD8 T cells display a preprogrammed chromatin accessibility profile and maintain a molecular history of cis-element usage, thereby reducing the steps necessary to revive effector functions.
引用
收藏
页码:2238 / 2243
页数:6
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