Kidins220 and Aiolos promote thymic iNKT cell development by reducing TCR signals

Kidins220 和 Aiolos 通过降低 TCR 信号促进胸腺 iNKT 细胞发育

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作者:Laurenz A Herr, Gina J Fiala, Sagar, Anna-Maria Schaffer, Jonas F Hummel, Marina Zintchenko, Katrin Raute, Rubí M-H Velasco Cárdenas, Beate Heizmann, Karolina Ebert, Kerstin Fehrenbach, Iga Janowska, Susan Chan, Yakup Tanriver, Susana Minguet, Wolfgang W Schamel

Abstract

Development of T cells is controlled by the signal strength of the TCR. The scaffold protein kinase D-interacting substrate of 220 kilodalton (Kidins220) binds to the TCR; however, its role in T cell development was unknown. Here, we show that T cell-specific Kidins220 knockout (T-KO) mice have strongly reduced invariant natural killer T (iNKT) cell numbers and modest decreases in conventional T cells. Enhanced apoptosis due to increased TCR signaling in T-KO iNKT thymocytes of developmental stages 2 and 3 shows that Kidins220 down-regulates TCR signaling at these stages. scRNA-seq indicated that the transcription factor Aiolos is down-regulated in Kidins220-deficient iNKT cells. Analysis of an Aiolos KO demonstrated that Aiolos is a downstream effector of Kidins220 during iNKT cell development. In the periphery, T-KO iNKT cells show reduced TCR signaling upon stimulation with α-galactosylceramide, suggesting that Kidins220 promotes TCR signaling in peripheral iNKT cells. Thus, Kidins220 reduces or promotes signaling dependent on the iNKT cell developmental stage.

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