DeFalco Tony, Potter Sarah J, Williams Alyna V, Waller Brittain, Kan Matthew J, Capel Blanche
Division of Reproductive Sciences, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Division of Reproductive Sciences, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Cell Rep. 2015 Aug 18;12(7):1107-19. doi: 10.1016/j.celrep.2015.07.015. Epub 2015 Aug 6.
The testis produces sperm throughout the male reproductive lifespan by balancing self-renewal and differentiation of spermatogonial stem cells (SSCs). Part of the SSC niche is thought to lie outside the seminiferous tubules of the testis; however, specific interstitial components of the niche that regulate spermatogonial divisions and differentiation remain undefined. We identified distinct populations of testicular macrophages, one of which lies on the surface of seminiferous tubules, in close apposition to areas of tubules enriched for undifferentiated spermatogonia. These macrophages express spermatogonial proliferation- and differentiation-inducing factors, such as colony-stimulating factor 1 (CSF1) and enzymes involved in retinoic acid (RA) biosynthesis. We show that transient depletion of macrophages leads to a disruption in spermatogonial differentiation. These findings reveal an unexpected role for macrophages in the spermatogonial niche in the testis and raise the possibility that macrophages play previously unappreciated roles in stem/progenitor cell regulation in other tissues.
睾丸通过平衡精原干细胞(SSCs)的自我更新和分化,在男性整个生殖寿命期内产生精子。部分SSC生态位被认为位于睾丸的生精小管之外;然而,调节精原细胞分裂和分化的生态位特定间质成分仍不明确。我们鉴定出了不同类型的睾丸巨噬细胞,其中一种位于生精小管表面,紧邻富含未分化精原细胞的小管区域。这些巨噬细胞表达精原细胞增殖和分化诱导因子,如集落刺激因子1(CSF1)以及参与视黄酸(RA)生物合成的酶。我们发现巨噬细胞的短暂耗竭会导致精原细胞分化受到破坏。这些发现揭示了巨噬细胞在睾丸精原细胞生态位中意想不到的作用,并增加了巨噬细胞在其他组织的干细胞/祖细胞调节中发挥此前未被认识到的作用的可能性。