T cell receptor signaling kinase dynamics after APC activation. Co-activating CD28 becomes deficient via immunosenescence thus corrupting T cell efficiency in the elderly. 26.10.2021 DJGPhD.
- Author
- Dr Daniel J. Guerra
- Published
- Wed 27 Oct 2021
- Episode Link
- https://podcasters.spotify.com/pod/show/dr-daniel-j-guerra/episodes/T-cell-receptor-signaling-kinase-dynamics-after-APC-activation--Co-activating-CD28-becomes-deficient-via-immunosenescence-thus-corrupting-T-cell-efficiency-in-the-elderly--26-10-2021-DJGPhD-e19c2qf
The Src-family kinase Lck regulates T-cell development, activation, proliferation, and immune synapse dynamics. These are the initiation phases of TCR signaling. Upon antigen presentation via the APC- TCR immune synapse, Lck phosphorylates tyrosine residues within the immunoreceptor tyrosine-based activation motifs (ITAMs) of the TCR-associated CD3 membrane protein domains.
Phosphorylated ITAMs function as a molecular platform for tandem SH2 domains located on the tyrosine kinase Zap-70, initially activated by Lck.
Lck kinase activity is regulated at two canonical phosphorylation sites Tyr394 and Tyr505, wherein auto-transphosphorylation of Tyr394 in the kinase domain erupts a relaxed/active conformation but phosphorylation of Tyr505, located at the C-terminus, by the tyrosine kinase Csk results in an inactive enzyme.
References
Longev Healthspan. 2012; 1: 6
SCIENCE ADVANCES•19 Jun 2019•Vol 5, Issue 6
