Sex-biased human thymic architecture guides T cell development through spatially defined niches

性别差异导致的人类胸腺结构通过空间定义的微环境引导T细胞发育

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作者:Laura N Stankiewicz ,Kevin Salim ,Emily A Flaschner ,Yu Xin Wang ,John M Edgar ,Lauren J Durland ,Bruce Z B Lin ,Grace C Bingham ,Matthew C Major ,Ross D Jones ,Helen M Blau ,Elizabeth J Rideout ,Megan K Levings ,Peter W Zandstra ,Fabio M V Rossi

Abstract

Within the thymus, regulation of the cellular crosstalk directing T cell development depends on spatial interactions within specialized niches. To create a spatially defined map of tissue niches guiding human postnatal T cell development, we employed the multidimensional imaging platform co-detection by indexing (CODEX) as well as cellular indexing of transcriptomes and epitopes sequencing (CITE-seq) and assay for transposase accessible chromatin sequencing (ATAC-seq). We generated age-matched 4- to 5-month-old human postnatal thymus datasets for male and female donors, identifying significant sex differences in both T cell and thymus biology. We demonstrate a possible role for JAG ligands in directing thymic-like dendritic cell development, identify important functions of a population of extracellular matrix (ECM)- fibroblasts, and characterize the medullary niches surrounding Hassall's corpuscles. Together, these data represent an age-matched spatial multiomic resource to investigate how sex-based differences in thymus regulation and T cell development arise, providing an essential resource to understand the mechanisms underlying immune function and dysfunction in males and females.

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