4.6 Article

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

Journal

JOURNAL OF IMMUNOLOGY
Volume 188, Issue 9, Pages 4145-4148

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1200176

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Funding

  1. National Institutes of Health [AI042370, AI061699, AI076458, T32HD007516, 3T32GM007170-36S1, T32GM07229, AI065644, DK080949, DP2OD008469]
  2. Abramson family

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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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