Early transcriptional and epigenetic regulation of CD8+ T cell differentiation revealed by single-cell RNA sequencing

被引:169
|
作者
Kakaradov, Boyko [1 ]
Arsenio, Janilyn [2 ]
Widjaja, Christella E. [2 ]
He, Zhaoren [1 ]
Aigner, Stefan [1 ]
Metz, Patrick J. [2 ]
Yu, Bingfei [3 ]
Wehrens, Ellen J. [3 ]
Lopez, Justine [2 ]
Kim, Stephanie H. [2 ]
Zuniga, Elina I. [3 ]
Goldrath, Ananda W. [3 ]
Chang, John T. [2 ]
Yeo, Gene W. [1 ,4 ,5 ]
机构
[1] Univ Calif San Diego, Dept Cellular & Mol Med, San Diego, CA 92103 USA
[2] Univ Calif San Diego, Dept Med, San Diego, CA 92103 USA
[3] Univ Calif San Diego, Div Biol Sci, San Diego, CA 92103 USA
[4] Univ Calif San Diego, Inst Genom Med, San Diego, CA 92103 USA
[5] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Physiol, Singapore, Singapore
基金
美国国家卫生研究院;
关键词
CENTRAL-MEMORY; EXPRESSION; EFFECTOR; SEQ; HETEROGENEITY; SIGNATURES; DIVISION; IMMUNE; BETA; EZH2;
D O I
10.1038/ni.3688
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
During microbial infection, responding CD8(+) T lymphocytes differentiate into heterogeneous subsets that together provide immediate and durable protection. To elucidate the dynamic transcriptional changes that underlie this process, we applied a single-cell RNA-sequencing approach and analyzed individual CD8(+) T lymphocytes sequentially throughout the course of a viral infection in vivo. Our analyses revealed a striking transcriptional divergence among cells that had undergone their first division and identified previously unknown molecular determinants that controlled the fate specification of CD8(+) T lymphocytes. Our findings suggest a model for the differentiation of terminal effector cells initiated by an early burst of transcriptional activity and subsequently refined by epigenetic silencing of transcripts associated with memory lymphocytes, which highlights the power and necessity of single-cell approaches.
引用
收藏
页码:422 / +
页数:14
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