Brief homogeneous TCR signals instruct common iNKT progenitors whose effector diversification is characterized by subsequent cytokine signaling
- PMID: 34562377
- DOI: 10.1016/j.immuni.2021.09.003 (VSports最新版本)
Brief homogeneous TCR signals instruct common iNKT progenitors whose effector diversification is characterized by subsequent cytokine signaling
Abstract
Innate-like T cell populations expressing conserved TCRs play critical roles in immunity through diverse developmentally acquired effector functions. Focusing on the prototypical lineage of invariant natural killer T (iNKT) cells, we sought to dissect the mechanisms and timing of fate decisions and functional effector differentiation. Utilizing induced expression of the semi-invariant NKT cell TCR on double positive thymocytes, an initially highly synchronous wave of iNKT cell development was triggered by brief homogeneous TCR signaling. After reaching a uniform progenitor state characterized by IL-4 production potential and proliferation, effector subsets emerged simultaneously, but then diverged toward different fates. While NKT17 specification was quickly completed, NKT1 cells slowly differentiated and expanded. NKT2 cells resembled maturing progenitors, which gradually diminished in numbers. Thus, iNKT subset diversification occurs in dividing progenitor cells without acute TCR input but utilizes multiple active cytokine signaling pathways VSports手机版. These data imply a two-step model of iNKT effector differentiation. .
Keywords: IL-17; IL-4; PLZF; agonist TCR signals; cytokine polarization; effector differentiation; gene expression dynamics; iNKT; innate T cell development; thymus V体育安卓版. .
Copyright © 2021 Elsevier Inc V体育ios版. All rights reserved. .
Conflict of interest statement
Declaration of interests The authors declare no competing interests.
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