
AbstractIdiopathic diseases of the reproductive system are important factors leading to male infertility. Many studies have shown that microRNAs (miRNAs) regulate the expression of multiple genes that play a significant role in spermatogenesis and development. We previously showed that microRNA-210 (miR-210) is one of the markedly upregulated microRNAs in the testes of sterile males with maturation arrest (MA). However, the role of miR-210 in spermatogenesis remains unknown. In this study, we found that miR-210 is highly expressed not only in patients with MA but also in patients with cryptorchidism. In addition, miR-210 inhibits the expression of Nuclear Receptor Subfamily 1, Group D, Member 2 (NR1D2) both in vitro and in vivo, particularly in cryptorchidic tissues. To facilitate further research, we established a mouse model of cryptorchidism and were surprised to discover that the miR-210 expression pattern was in accordance with that of patients with cryptorchidism. Thus, we propose that miR-210 may serve as a biomarker of cryptorchidism in clinical tests.
Male, Receptors, Cytoplasmic and Nuclear, Article, Spermatogonia, Up-Regulation, Repressor Proteins, Mice, MicroRNAs, HEK293 Cells, Gene Expression Regulation, Cell Line, Tumor, Cryptorchidism, Testis, Animals, Humans, Spermatogenesis, Azoospermia
Male, Receptors, Cytoplasmic and Nuclear, Article, Spermatogonia, Up-Regulation, Repressor Proteins, Mice, MicroRNAs, HEK293 Cells, Gene Expression Regulation, Cell Line, Tumor, Cryptorchidism, Testis, Animals, Humans, Spermatogenesis, Azoospermia
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