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PNAS Plus: Yolk-sac–derived macrophages regulate fetal testis vascularization and morphogenesis

机译:PNAS Plus:卵黄囊来源的巨噬细胞调节胎儿睾丸的血管形成和形态发生

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摘要

Organogenesis of the testis is initiated when expression of Sry in pre-Sertoli cells directs the gonad toward a male-specific fate. The cells in the early bipotential gonad undergo de novo organization to form testis cords that enclose germ cells inside tubules lined by epithelial Sertoli cells. Although Sertoli cells are a driving force in the de novo formation of testis cords, recent studies in mouse showed that reorganization of the vasculature and of interstitial cells also play critical roles in testis cord morphogenesis. However, the mechanism driving reorganization of the vasculature during fetal organogenesis remained unclear. Here we demonstrate that fetal macrophages are associated with nascent gonadal and mesonephric vasculature during the initial phases of testis morphogenesis. Macrophages mediate vascular reorganization and prune errant germ cells and somatic cells after testis architecture is established. We show that gonadal macrophages are derived from primitive yolk-sac hematopoietic progenitors and exhibit hallmarks of M2 activation status, suggestive of angiogenic and tissue remodeling functions. Depletion of macrophages resulted in impaired vascular reorganization and abnormal cord formation. These findings reveal a previously unappreciated role for macrophages in testis morphogenesis and suggest that macrophages are an intermediary between neovascularization and organ architecture during fetal organogenesis.
机译:当Sertoli细胞中Sry的表达将性腺引导至男性特异性命运时,就会开始睾丸的器官发生。早期双电位性腺中的细胞从头组织,形成睾丸索,将生殖细胞包裹在上皮支持细胞衬里的小管内。尽管支持细胞是睾丸线从头形成的驱动力,但最近在小鼠中的研究表明,脉管系统和间质细胞的重组在睾丸线的形态发生中也起着关键作用。然而,在胎儿器官发生过程中驱动脉管系统重组的机制仍不清楚。在这里,我们证明胎儿巨噬细胞在睾丸形态发生的初始阶段与新生的性腺和中肾血管相关。建立睾丸结构后,巨噬细胞介导血管重组以及修剪的生殖细胞和体细胞。我们表明,性腺巨噬细胞源于原始卵黄囊造血祖细胞,并表现出M2激活状态的标志,提示血管生成和组织重塑功能。巨噬细胞的耗竭导致血管重组受损和异常的脐带形成。这些发现揭示了巨噬细胞在睾丸形态发生中以前没有被认识到的作用,并表明巨噬细胞是胎儿器官发生过程中新血管形成与器官结构之间的中介。

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