Journal
CELL REPORTS
Volume 39, Issue 11, Pages -Publisher
CELL PRESS
DOI: 10.1016/j.celrep.2022.110935
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Funding
- Swiss National Science Foundation [31003A_173070, 310030_200316]
- Departement de l'Instruction Publique of the State of Geneva
- Swiss National Science Foundation (SNF) [31003A_173070, 310030_200316] Funding Source: Swiss National Science Foundation (SNF)
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Single-cell transcriptomics reveal the complex origin and differentiation dynamics of androgen-producing cells in mice, including the origin and evolution of steroidogenic progenitors. The study also highlights the important role of Wnt5a gene in the formation of androgen-producing cells and peritubular myoid cells.
Leydig cells (LCs) are the major androgen-producing cells in the testis. They arise from steroidogenic progenitors (SPs), whose origins, maintenance, and differentiation dynamics remain largely unknown. Single-cell transcriptomics reveal that the mouse steroidogenic lineage is specified as early as embryonic day 12.5 (E12.5) and has a dual mesonephric and coelomic origin. SPs specifically express the Wnt5a gene and evolve rapidly. At E12.5 and E13.5, they give rise first to an intermediate population of pre-LCs, and finally to fetal LCs. At E16.5, SPs possess the characteristics of the dormant progenitors at the origin of adult LCs and are also transcriptionally closely related to peritubular myoid cells (PMCs). In agreement with our in silico analysis, in vivo lineage tracing indicates that Wnt5a-expressing cells are bona fide progenitors of PMCs as well as fetal and adult LCs, contributing to most of the LCs present in the fetal and adult testis.
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