SLP-76 interaction with PLC-γ1 fine-tunes TCR signal strength for appropriate thymocyte selection, T cell homeostasis, and Ag-specific T cell response
نویسندگان
چکیده
Abstract TCR signal strength regulates T cell fate at various stages of thymocyte development and the differentiation peripheral cells into distinct subsets. We previously showed that engagement forms a heterotetrametric complex composed LAT, Gads, SLP-76, PLC-γ1 this is essential to activate further transduce signal. The interaction SLP-76 proline-rich region (PRR) with SH3 domain relatively weak, these two domains are highly conserved amongst many mammalian species. Therefore, we hypothesized PRR sequence low affinity for might be evolutionarily favored prevent excess signals. To test hypothesis, developed mice carrying conditional cell-specific knock-in mutation in 2.5-fold increased by CRISPR/Cas9-mediated gene editing Cre/LoxP system (cKI). Notably, cKI expression active caspase-3 signaled SP4 SP8 thymocytes decreased numbers mature medullary thymocytes, suggestive enhanced negative selection. Under steady-state conditions, generation CD8 +central memory cells, implying an sensitivity self-Ag/MHC I periphery. Moreover, rendered +T more sensitive OVA altered peptide ligands weaker OT-I TCR. Finally, priming had not undergone massive divisions IFNγ-producing effectors vivo, weakly activated cognate Ag. Our data indicate PRR/PLC-γ1 plays critical role fine-tuning avoid signals via NCI/NIH Intramural Support
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ژورنال
عنوان ژورنال: Journal of Immunology
سال: 2023
ISSN: ['1550-6606', '0022-1767']
DOI: https://doi.org/10.4049/jimmunol.210.supp.154.14