Cooperative interaction of Nck and Lck orchestrates optimal TCR signaling

Abstract: The T cell antigen receptor (TCR) is expressed on T cells, which orchestrate adaptive immune responses. It is composed of the ligand-binding clonotypic TCRαβ heterodimer and the non-covalently bound invariant signal-transducing CD3 complex. Among the CD3 subunits, the CD3ε cytoplasmic tail contains binding motifs for the Src family kinase, Lck, and the adaptor protein, Nck. Lck binds to a receptor kinase (RK) motif and Nck binds to a proline-rich sequence (PRS). Both motifs only become accessible upon ligand binding to the TCR and facilitate the recruitment of Lck and Nck independently of phosphorylation of the TCR. Mutations in each of these motifs cause defects in TCR signaling and T cell activation. Here, we investigated the role of Nck in proximal TCR signaling by silencing both Nck isoforms, Nck1 and Nck2. In the absence of Nck, TCR phosphorylation, ZAP70 recruitment, and ZAP70 phosphorylation was impaired. Mechanistically, this is explained by loss of Lck recruitment to the stimulated TCR in cells lacking Nck. Hence, our data uncover a previously unknown cooperative interaction between Lck and Nck to promote optimal TCR signaling

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
Cells. - 10, 4 (2021) , 834, ISSN: 2073-4409

Ereignis
Veröffentlichung
(wo)
Freiburg
(wer)
Universität
(wann)
2021
Urheber
Hartl, Frederike A
Ngoenkam, Jatuporn
Beck-García, Esmeralda
Cerqueira, Liz
Wipa, Piyamaporn
Paensuwan, Pussadee
Suriyaphol, Prapat
Mishra, Pankaj
Schraven, Burkhart
Günther, Stefan
Pongcharoen, Sutatip
Schamel, Wolfgang
Minguet, Susana

DOI
10.3390/cells10040834
URN
urn:nbn:de:bsz:25-freidok-1949122
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Letzte Aktualisierung
14.08.2025, 10:57 MESZ

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  • 2021

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