Interaction between γδTCR signaling and the E protein‐Id axis in γδ T cell development

• Published in: Immunological reviews Vol. 298; no. 1; pp. 181 - 197
• Main Authors: Anderson, Michele K., Selvaratnam, Johanna S.
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.11.2020
• Subjects: Chemokine receptors; Cytokines; E protein; Lymphocytes; Lymphocytes T; Medulla oblongata; Ontogeny; Proteins; Signal strength; Signaling; Thymus; Windows (intervals)
• ISSN: 0105-2896; 1600-065X
• DOI: 10.1111/imr.12924

γδ T cells acquire their functional properties in the thymus, enabling them to exert rapid innate‐like responses. To understand how distinct γδ T cell subsets are generated, we have developed a Two‐Stage model for γδ T cell development. This model is predicated on the finding that γδTCR signal strength impacts E protein activity through graded upregulation of Id3. Our model proposes that cells enter Stage 1 in response to a γδTCR signaling event in the cortex that activates a γδ T cell–specific gene network. Part of this program includes the upregulation of chemokine receptors that guide them to the medulla. In the medulla, Stage 1 cells receive distinct combinations of γδTCR, cytokine, and/co‐stimulatory signals that induce their transit into Stage 2, either toward the γδT1 or the γδT17 lineage. The intersection between γδTCR and cytokine signals can tune Id3 expression, leading to different outcomes even in the presence of strong γδTCR signals. The thymic signaling niches required for γδT17 development are segregated in time and space, providing transient windows of opportunity during ontogeny. Understanding the regulatory context in which E proteins operate at different stages will be key in defining how their activity levels impose functional outcomes.