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Integrative analysis of scRNA-seq and scATAC-seq revealed transit-amplifying thymic epithelial cells expressing autoimmune regulator.

Takahisa MiyaoMaki MiyauchiS Thomas KellyTommy W TerooateaTatsuya IshikawaEugene OhSotaro HiraiKenta HorieYuki TakakuraHouko OhkiMio HayamaYuya MaruyamaTakao SekiHiroto IshiiHaruka YabukamiMasaki YoshidaAzusa InoueAsako Sakaue-SawanoAtsushi MiyawakiMasafumi MurataniAki MinodaNobuko AkiyamaTaishin Akiyama
Published in: eLife (2022)
Medullary thymic epithelial cells (mTECs) are critical for self-tolerance induction in T cells via promiscuous expression of tissue-specific antigens (TSAs), which are controlled by the transcriptional regulator, AIRE. Whereas AIRE-expressing (Aire + ) mTECs undergo constant turnover in the adult thymus, mechanisms underlying differentiation of postnatal mTECs remain to be discovered. Integrative analysis of single-cell assays for transposase-accessible chromatin (scATAC-seq) and single-cell RNA sequencing (scRNA-seq) suggested the presence of proliferating mTECs with a specific chromatin structure, which express high levels of Aire and co-stimulatory molecules, CD80 (Aire + CD80 hi ). Proliferating Aire + CD80 hi mTECs detected using Fucci technology express a minimal number of Aire-dependent TSAs and are converted into quiescent Aire + CD80 hi mTECs expressing high levels of TSAs after a transit amplification. These data provide evidence for the existence of transit-amplifying Aire + mTEC precursors during the Aire + mTEC differentiation process of the postnatal thymus.
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