| Literature DB >> 34407418 |
Yoshifumi Mori1, Seiji Takashima1, Mito Kanatsu-Shinohara2, Zheng Yi3, Takashi Shinohara4.
Abstract
Spermatogonial stem cells (SSCs) are maintained in a special microenvironment called a niche. However, much is unknown about components that constitute the niche. Here, we report that Cdc42 is essential for germline niche development. Sertoli cell-specific Cdc42-deficient mice showed normal premeiotic spermatogenesis. However, germ cells gradually disappeared during haploid cell formation and few germ cells remained in the mature testes. Spermatogonial transplantation experiments revealed a significant loss of SSCs in Cdc42-deficient testes. Moreover, Cdc42 deficiency in Sertoli cells downregulated GDNF, a critical factor for SSC maintenance. Cdc42-deficient Sertoli cells also exhibited lower nuclear MAPK1/3 staining. Inhibition of MAP2K1 or depletion of Pea15a scaffold protein downregulated GDNF expression. A screen of transcription factors revealed that Cdc42-deficient Sertoli cells downregulate DMRT1 and SOX9, both of which are critical for Sertoli cell development. These results indicate that Cdc42 is essential for niche function via MAPK1/3-dependent GDNF secretion.Entities:
Keywords: CDC42; DMRT1; GDNF; MAP2K1; SOX9; niche; spermaogonial stem cells
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Year: 2021 PMID: 34407418 DOI: 10.1016/j.celrep.2021.109550
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423