Intensity and duration of TCR signaling is limited by p38 phosphorylation of ZAP-70T293 and destabilization of the signalosome.
Maria Letizia Giardino TorchiaDebjani DuttaPaul R MittelstadtJune GuhaMatthias M GaidaKamonwan FishValarie A BarrItoro O AkpanLawrence E SamelsonHarichandra D TagadSubrata DebnathLisa M Miller JenkinsEttore AppellaJonathan D AshwellPublished in: Proceedings of the National Academy of Sciences of the United States of America (2018)
ZAP-70 is a tyrosine kinase that is essential for initiation of T cell antigen receptor (TCR) signaling. We have found that T cell p38 MAP kinase (MAPK), which is directly phosphorylated and activated by ZAP-70 downstream of the TCR, in turn phosphorylates Thr-293 in the interdomain B region of ZAP-70. Mutant T cells expressing ZAP-70 with an alanine substitution at this residue (ZAP-70T293A) had enhanced TCR proximal signaling and increased effector responses. Lack of ZAP-70T293 phosphorylation increased association of ZAP-70 with the TCR and prolonged the existence of TCR signaling microclusters. These results identify a tight negative feedback loop in which ZAP-70-activated p38 reciprocally phosphorylates ZAP-70 and destabilizes the signaling complex.