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

Sci Adv. 2024 Mar 15;10(11):eadj2802. doi: 10.1126/sciadv.adj2802. Epub 2024 Mar 15.

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.

MeSH terms

  • Animals
  • Cell Differentiation
  • Gene Expression Regulation
  • Ikaros Transcription Factor* / metabolism
  • Membrane Proteins* / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Natural Killer T-Cells* / metabolism
  • Receptors, Antigen, T-Cell / metabolism
  • Signal Transduction
  • Thymus Gland* / cytology
  • Thymus Gland* / metabolism

Substances

  • Receptors, Antigen, T-Cell
  • Kidins220 protein, mouse
  • Ikzf3 protein, mouse
  • Membrane Proteins
  • Ikaros Transcription Factor