| Literature DB >> 30420628 |
Jinsung Hong1,2,3, Chenghao Ge2,4, Prithiviraj Jothikumar2,4, Zhou Yuan2,4, Baoyu Liu2,4,5, Ke Bai2,4,6, Kaitao Li2,4, William Rittase1,2, Miho Shinzawa7, Yun Zhang8, Amy Palin9,10, Paul Love9, Xinhua Yu11, Khalid Salaita8, Brian D Evavold12,5, Alfred Singer7, Cheng Zhu13,14,15.
Abstract
The T cell antigen receptor (TCR) expressed on thymocytes interacts with self-peptide major histocompatibility complex (pMHC) ligands to signal apoptosis or survival. Here, we found that negative-selection ligands induced thymocytes to exert forces on the TCR and the co-receptor CD8 and formed cooperative TCR-pMHC-CD8 trimolecular 'catch bonds', whereas positive-selection ligands induced less sustained thymocyte forces on TCR and CD8 and formed shorter-lived, independent TCR-pMHC and pMHC-CD8 bimolecular 'slip bonds'. Catch bonds were not intrinsic to either the TCR-pMHC or the pMHC-CD8 arm of the trans (cross-junctional) heterodimer but resulted from coupling of the extracellular pMHC-CD8 interaction to the intracellular interaction of CD8 with TCR-CD3 via associated kinases to form a cis (lateral) heterodimer capable of inside-out signaling. We suggest that the coupled trans-cis heterodimeric interactions form a mechanotransduction loop that reinforces negative-selection signaling that is distinct from positive-selection signaling in the thymus.Entities:
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Year: 2018 PMID: 30420628 PMCID: PMC6452639 DOI: 10.1038/s41590-018-0259-z
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606