CD8αα intraepithelial lymphocytes arise from two main thymic precursors

Roland Ruscher, Rebecca L. Kummer, You Jeong Lee, Stephen C. Jameson, Kristin A. Hogquist

Research output: Contribution to journalArticlepeer-review

40 Scopus citations

Abstract

TCRαβ + CD4 CD8α + CD8β intestinal intraepithelial lymphocytes (CD8αα IELs) are an abundant population of thymus-derived T cells that protect the gut barrier surface. We sought to better define the thymic IEL precursor (IELp) through analysis of its maturation, localization and emigration. We defined two precursor populations among TCRβ + CD4 CD8 thymocytes by dependence on the kinase TAK1 and rigorous lineage-exclusion criteria. Those IELp populations included a nascent PD-1 + population and a T-bet + population that accumulated with age. Both gave rise to intestinal CD8αα IELs after adoptive transfer. The PD-1 + IELp population included more strongly self-reactive clones and was largely restricted by classical major histocompatibility complex (MHC) molecules. Those cells localized to the cortex and efficiently emigrated in a manner dependent on the receptor S1PR1. The T-bet + IELp population localized to the medulla, included cells restricted by non-classical MHC molecules and expressed the receptor NK1.1, the integrin CD103 and the chemokine receptor CXCR3. The two IELp populations further differed in their use of the T cell antigen receptor (TCR) α-chain variable region (V α) and β-chain variable region (V β). These data provide a foundation for understanding the biology of CD8αα IELs.

Original languageEnglish (US)
Pages (from-to)771-779
Number of pages9
JournalNature immunology
Volume18
Issue number7
DOIs
StatePublished - Jun 20 2017

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