Handel Adam E, Cheuk Stanley, Dhalla Fatima, Maio Stefano, Hübscher Tania, Rota Ioanna, Deadman Mary E, Ekwall Olov, Lütolf Matthias, Weinberg Kenneth, Holländer Georg
Department of Paediatrics and the Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Sci Adv. 2022 May 13;8(19):eabm9844. doi: 10.1126/sciadv.abm9844.
The thymic stroma is composed of epithelial and nonepithelial cells providing separate microenvironments controlling homing, differentiation, and selection of hematopoietic precursor cells to functional T cells. Here, we explore at single-cell resolution the complex composition and dynamic changes of the nonepithelial stromal compartment across different developmental stages in the human and mouse thymus, and in an experimental model of the DiGeorge syndrome, the most common form of human thymic hypoplasia. The detected gene expression signatures identify previously unknown stromal subtypes and relate their individual molecular profiles to separate differentiation trajectories and functions, revealing an unprecedented heterogeneity of different cell types that emerge at discrete developmental stages and vary in their expression of key regulatory signaling circuits and extracellular matrix components. Together, these findings highlight the dynamic complexity of the nonepithelial thymus stroma and link this to separate instructive roles essential for normal thymus organogenesis and tissue maintenance.
胸腺基质由上皮细胞和非上皮细胞组成,它们提供独立的微环境,控制造血前体细胞归巢、分化以及向功能性T细胞的选择过程。在此,我们以单细胞分辨率探究了人类和小鼠胸腺不同发育阶段以及DiGeorge综合征(人类胸腺发育不全最常见的形式)实验模型中非上皮基质区室的复杂组成和动态变化。检测到的基因表达特征识别出了以前未知的基质亚型,并将它们各自的分子谱与不同的分化轨迹和功能联系起来,揭示了在离散发育阶段出现的不同细胞类型前所未有的异质性,这些细胞类型在关键调节信号通路和细胞外基质成分的表达上存在差异。这些发现共同突出了非上皮胸腺基质的动态复杂性,并将其与正常胸腺器官发生和组织维持所必需的不同指导作用联系起来。