Divergent molecular events underlying initial T-cell commitment in human prenatal and postnatal thymus

Front Immunol. 2023 Sep 27:14:1240859. doi: 10.3389/fimmu.2023.1240859. eCollection 2023.

Abstract

Introduction: Intrathymic T-cell development is a coordinated process accompanied by dynamic changes in gene expression. Although the transcriptome characteristics of developing T cells in both human fetal and postnatal thymus at single-cell resolution have been revealed recently, the differences between human prenatal and postnatal thymocytes regarding the ontogeny and early events of T-cell development still remain obscure. Moreover, the transcriptional heterogeneity and posttranscriptional gene expression regulation such as alternative polyadenylation at different stages are also unknown.

Method: In this study, we performed integrative single-cell analyses of thymocytes at distinct developmental stages.

Results: The subsets of prenatal CD4-CD8- double-negative (DN) cells, the most immature thymocytes responsible for T-cell lineage commitment, were characterized. By comprehensively comparing prenatal and postnatal DN cells, we revealed significant differences in some key gene expressions. Specifically, prenatal DN subpopulations exhibited distinct biological processes and markedly activated several metabolic programs that may be coordinated to meet the required bioenergetic demands. Although showing similar gene expression patterns along the developmental path, prenatal and postnatal thymocytes were remarkably varied regarding the expression dynamics of some pivotal genes for cell cycle, metabolism, signaling pathway, thymus homing, and T-cell commitment. Finally, we quantified the transcriptome-wide changes in alternative polyadenylation across T-cell development and found diverse preferences of polyadenylation site usage in divergent populations along the T-cell commitment trajectory.

Discussion: In summary, our results revealed transcriptional heterogeneity and a dynamic landscape of alternative polyadenylation during T-cell development in both human prenatal and postnatal thymus, providing a comprehensive resource for understanding T lymphopoiesis in human thymus.

Keywords: T cell development; alternative polyadenylation; double-negative thymocytes; human thymus; scRNA-seq.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Differentiation / genetics
  • Female
  • Humans
  • Pregnancy
  • Signal Transduction
  • Thymocytes*
  • Thymus Gland* / metabolism

Grants and funding

This study was supported by grants from the National Key R&D Program of China (2022YFA1103501, 2020YFA0112400, and 2021YFA1100102), the National Natural Science Foundation of China (81890991, 31930054, 82200121, and 82270118), the Program for Guangdong Introducing Innovative and Entrepreneurial Teams (2017ZT07S347), China National Postdoctoral Program for Innovative Talents (BX20220134), and China Postdoctoral Science Foundation (2021M701432).