Pre-T cell receptor localization and trafficking are independent of its signaling

• Published in: The Journal of cell biology Vol. 222; no. 10; p. 1
• Main Authors: Smid, Andrei I, Garforth, Sam J, Obaid, Maryam S, Bollons, Hannah R, James, John R
• Format: Journal Article
• Language: English
• Published: United States Rockefeller University Press 02.10.2023
• Subjects: Adaptive systems; Cell Membrane; Cell Signaling; Cell surface; Hydrophobicity; Immune system; Immunology; Ligands; Localization; Lymphocytes; Lymphocytes T; Protein transport; Receptor mechanisms; Receptors; Receptors, Antigen, T-Cell - genetics; Signal Transduction; T cell receptors
• ISSN: 0021-9525; 1540-8140; 1540-8140
• DOI: 10.1083/jcb.202212106

Expression of the pre-T cell receptor (preTCR) is an important checkpoint during the development of T cells, an essential cell type of our adaptive immune system. The preTCR complex is only transiently expressed and rapidly internalized in developing T cells and is thought to signal in a ligand-independent manner. However, identifying a mechanistic basis for these unique features of the preTCR compared with the final TCR complex has been confounded by the concomitant signaling that is normally present. Thus, we have reconstituted preTCR expression in non-immune cells to uncouple receptor trafficking dynamics from its associated signaling. We find that all the defining features of the preTCR are intrinsic properties of the receptor itself, driven by exposure of an extracellular hydrophobic region, and are not the consequence of receptor activation. Finally, we show that transitory preTCR cell surface expression can sustain tonic signaling in the absence of ligand binding, suggesting how the preTCR can nonetheless drive αβTCR lineage commitment.