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Cutting Edge: Asymmetric Memory T Cell Division in Response to Rechallenge
被引:59
作者:

Ciocca, Maria L.
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Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
Univ Penn, Perelman Sch Med, Dept Med, Philadelphia, PA 19104 USA Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA

Barnett, Burton E.
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机构:
Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
Univ Penn, Perelman Sch Med, Dept Med, Philadelphia, PA 19104 USA Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA

Burkhardt, Janis K.
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h-index: 0
机构:
Univ Penn, Perelman Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA

Chang, John T.
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h-index: 0
机构:
Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA

Reiner, Steven L.
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h-index: 0
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Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
Univ Penn, Perelman Sch Med, Dept Med, Philadelphia, PA 19104 USA Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
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.
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页码:4145 / 4148
页数:4
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