4.8 Article

The Lineage Differentiation and Dynamic Heterogeneity of Thymic Epithelial Cells During Thymus Organogenesis

期刊

FRONTIERS IN IMMUNOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2022.805451

关键词

thymic epithelial cells; dynamic heterogeneity; thymus organogenesis; cell differentiation; mTEC; cTEC

资金

  1. Longhua District Science and Technology Innovation Fund [201803]
  2. Longhua District Key Laboratory of Genomics and Precision Medicine [20170913A0410026]
  3. Guangdong Basic and Applied Basic Research Foundation [2019A1515011009, 2021A1515010683, 2020A1515010225, 2021A1515010955]
  4. Shenzhen Foundation of Science and Technology [JCYJ20180306172449376, JCYJ20180306172459580, JCYJ20180306172502097]
  5. Shenzhen Longhua District Foundation of Science and Technology [SZLHQJCYJ202002]

向作者/读者索取更多资源

The study utilized single-cell transcriptome analysis to reveal the transcriptional heterogeneity and cellular state evolution during thymic epithelial cell development, identifying the molecular nature and differentiation dynamics of TECs, as well as a population of mTECs expressing adult stem cell markers.
Although much progress has been made recently in revealing the heterogeneity of the thymic stromal components, the molecular programs of cell lineage divergency and temporal dynamics of thymic epithelial cell (TEC) development are largely elusive. Here, we constructed a single-cell transcriptional landscape of non-hematopoietic cells from mouse thymus spanning embryonic to adult stages, producing transcriptomes of 30,959 TECs. We resolved the transcriptional heterogeneity of developing TECs and highlighted the molecular nature of early TEC lineage determination and cortico-medullary thymic epithelial cell lineage divergency. We further characterized the differentiation dynamics of TECs by clarification of molecularly distinct cell states in the thymus developing trajectory. We also identified a population of Bpifa1(+) Plet1(+) mTECs that was preserved during thymus organogenesis and highly expressed tissue-resident adult stem cell markers. Finally, we highlighted the expression of Aire-dependent tissue-restricted antigens mainly in Aire(+) Csn2(+) mTECs and Spink5(+) Dmkn(+) mTECs in postnatal thymus. Overall, our data provided a comprehensive characterization of cell lineage differentiation, maturation, and temporal dynamics of thymic epithelial cells during thymus organogenesis.

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