a role for the immediate early gene product c-fos in imprinting t cells with short-term memory for signal summation立即早期基因的作用产品c-fos印记与短期记忆t细胞信号求和.pdfVIP

a role for the immediate early gene product c-fos in imprinting t cells with short-term memory for signal summation立即早期基因的作用产品c-fos印记与短期记忆t细胞信号求和.pdf

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a role for the immediate early gene product c-fos in imprinting t cells with short-term memory for signal summation立即早期基因的作用产品c-fos印记与短期记忆t细胞信号求和

A Role for the Immediate Early Gene Product c-fos in Imprinting T Cells with Short-Term Memory for Signal Summation 1,2 3 1,2 Carolyn E. Clark , Milena Hasan , Philippe Bousso * 1 Institut Pasteur, Dynamics of Immune Responses Unit, Paris, France, 2 Inserm U668, Paris, France, 3 Institut Pasteur, Center For Human Immunology, Paris, France Abstract T cells often make sequential contacts with multiple DCs in the lymph nodes and are likely to be equipped with mechanisms that allow them to sum up the successive signals received. We found that a period of stimulation as short as two hours could imprint on a T cell a ‘‘biochemical memory’’ of that activation signal that persisted for several hours. This was evidenced by more rapid induction of activation markers and earlier commitment to proliferation upon subsequent stimulation, even when that secondary stimulation occurred hours later. Upregulation of the immediate early gene product c-fos, a component of the AP-1 transcription factor, was maximal by 1–2 hours of stimulation, and protein levels remained elevated for several hours after stimulus withdrawal. Moreover, phosphorylated forms of c-fos that are stable and transcriptionally active persisted for a least a day. Upon brief antigenic stimulation in vivo, we also observed a rapid upregulation of c-fos that could be boosted by subsequent stimulation. Accumulation of phosphorylated c-fos may therefore serve as a biochemical fingerprint of previous suboptimal stimulation, leaving the T cell poised to rapidly resume its activation program upon its next en

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