Proliferating CD4 super(+) T Cells Undergo Immediate Growth Arrest upon Cessation of TCR Signaling In Vivo

To investigate the role of TCR signaling in the exit of CD4 super(+) 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 af...

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Veröffentlicht in:The Journal of immunology (1950) 2008-01, Vol.180 (1), p.156-162
Hauptverfasser: Yarke, Cory A, Dalheimer, Stacy L, Zhang, Na, Catron, Drew M, Jenkins, Marc K, Mueller, Daniel L
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container_title The Journal of immunology (1950)
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creator Yarke, Cory A
Dalheimer, Stacy L
Zhang, Na
Catron, Drew M
Jenkins, Marc K
Mueller, Daniel L
description To investigate the role of TCR signaling in the exit of CD4 super(+) 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 G sub(1)->SG sub(2)M phase cell cycle progression. As a consequence, clonal expansion in the absence of durable TCR signaling decreased by two-thirds. Thus, CD4 super(+) T cells scan for the presence Ag throughout their clonal expansion response, and continuously adjust their rate of cell growth and G sub(1)->S phase transition to match their intensity of TCR signaling.
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title Proliferating CD4 super(+) T Cells Undergo Immediate Growth Arrest upon Cessation of TCR Signaling In Vivo
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