ARHGEF15 in Sertoli cells contributes to germ cell development and testicular immune privilege†

Guanylate exchange factor Arhgef15 is required for the development of germ cells by maintaining the balance of immune-related factors in mouse testes. Sertoli cells (SCs), the only somatic cells in the seminiferous tubules, facilitate the maintenance of testicular immune privilege through the formation of the blood-testis barrier (BTB) and the expression of immunoregulatory factors. Rho guanosine exchange factor 15 (ARHGEF15) is a member of the guanosine exchange factors, which are involved in cell migration, cell polarity, and cell cycle progression via activation of Rho GTPases. This study investigated the functional role of ARHGEF15 in SCs during spermatogenesis using SC-specific Arhgef15 knockout mice. The results revealed that Arhgef15 deficiency in SCs affected the localization of SC nuclei, disrupted BTB integrity, and led to premature shedding of germ cells. In Arhgef15(flox/flox)/Amh-Cre(+) mice, the ultrastructure of the round spermatids was impaired, accompanied by acrosome degeneration, acrosomal vesicle shedding, and atrophic nuclei. Consequently, the percentage of abnormal sperm in the Arhgef15(flox/flox)/Amh-Cre(+) epididymis was markedly elevated. RNA-sequencing analysis revealed that most of the differentially expressed genes in SCs of Arhgef15(flox/flox)/Amh-Cre(+) mice were associated with immunity. Further study revealed that the sera of Arhgef15(flox/flox)/Amh-Cre(+) mice showed immunoreactivity against testicular lysate of wild-type mice, indicating the production of antibodies against testicular autoantigens in Arhgef15(flox/flox)/Amh-Cre(+) mice. In conclusion, the specific deletion of Arhgef15 in SCs of mice leads to sperm abnormality, probably by disrupting the testicular immune homeostasis.

Automated summary

This study revealed that specific deletion of Arhgef15 in Sertoli cells of mice leads to sperm abnormality, disruption of BTB integrity, and potentially affects testicular immune homeostasis.