| Literature DB >> 18097015 |
Cory A Yarke1, Stacy L Dalheimer, Na Zhang, Drew M Catron, Marc K Jenkins, Daniel L Mueller.
Abstract
To investigate the role of TCR signaling in the exit of CD4+ T cells from cell cycle, we took advantage of a low frequency TEa T cell adoptive transfer technique as well as the Y-Ae mAb to interrupt Ag/MHC recognition before the completion of clonal expansion. Termination of TCR signaling after 36 h of Ag exposure caused an immediate reduction in cell size and deceleration of G1->SG2M phase cell cycle progression. As a consequence, clonal expansion in the absence of durable TCR signaling decreased by two-thirds. Thus, CD4+ T cells scan for the presence Ag throughout their clonal expansion response, and continuously adjust their rate of cell growth and G1->S phase transition to match their intensity of TCR signaling.Entities:
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Year: 2008 PMID: 18097015 DOI: 10.4049/jimmunol.180.1.156
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422