Cutting Edge: Asymmetric Memory T Cell Division in Response to Rechallenge

被引:59
作者
Ciocca, Maria L. [1 ,2 ]
Barnett, Burton E. [1 ,2 ]
Burkhardt, Janis K. [3 ,4 ]
Chang, John T. [5 ]
Reiner, Steven L. [1 ,2 ]
机构
[1] Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Dept Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[4] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[5] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
IMMUNOLOGICAL SYNAPSE; LYMPHOCYTE DIVISION; EFFECTOR FUNCTIONS; SUBSETS; SEGREGATION; POLARITY;
D O I
10.4049/jimmunol.1200176
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Clonal selection of a T cell for use in the immune response appears to necessitate proliferative expansion and terminal effector differentiation of some cellular progeny, while reserving other progeny as less-differentiated memory cells. It has been suggested that asymmetric cell division may promote initial cell diversification. Stem cell-like models of adaptive immunity might predict that subsequent encounters with a pathogen would evoke reiterative, self-renewing, asymmetric division by memory T cells. In this study, we show that murine memory CD8(+) T cells can divide asymmetrically in response to secondary encounter with pathogen. Critical regulators of signaling and transcription are partitioned to one side of the mitotic spindle in rechallenged memory T cells, and two phenotypically distinct populations of daughter cells are evident from the earliest divisions. Memory T cells may thus use asymmetric cell division to generate cellular heterogeneity when faced with pathogen rechallenge. The Journal of Immunology, 2012, 188: 4145-4148.
引用
收藏
页码:4145 / 4148
页数:4
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