Distinct Expression Profiles and Novel Targets of MicroRNAs in Human Spermatogonia, Pachytene Spermatocytes, and Round Spermatids between OA Patients and NOA Patients

• Published in: Molecular therapy. Nucleic acids Vol. 9; no. C; pp. 182 - 194
• Main Authors: Yao, Chencheng, Yuan, Qingqing, Niu, Minghui, Fu, Hongyong, Zhou, Fan, Zhang, Wenhui, Wang, Hong, Wen, Liping, Wu, Ligang, Li, Zheng, He, Zuping
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.12.2017; Elsevier Limited; American Society of Gene & Cell Therapy; Elsevier
• Subjects: Biosynthesis; Chromosomes; DNA methylation; Epigenetics; Etiology; Genes; Genetic factors; human spermatogonia; Infertility; Meiosis; MicroRNAs; miRNA; Mitosis; Pachytene; pachytene spermatocytes; Proteins; round spermatids; Sedimentation; Spermatids; Spermatocytes; Spermatogenesis; Spermatogonia; Spermiogenesis; Stem cells; targeting genes; Transcription factors; microRNAs; human spermatogonia; round spermatids; pachytene spermatocytes; targeting genes
• ISSN: 2162-2531; 2162-2531
• DOI: 10.1016/j.omtn.2017.09.007

Human spermatogenesis includes three main stages, namely, the mitosis of spermatogonia, meiosis of spermatocytes, and spermiogenesis of spermatids, which are precisely regulated by epigenetic and genetic factors. Abnormality of epigenetic and genetic factors can result in aberrant spermatogenesis and eventual male infertility. However, epigenetic regulators in controlling each stage of normal and abnormal human spermatogenesis remain unknown. Here, we have revealed for the first time the distinct microRNA profiles in human spermatogonia, pachytene spermatocytes, and round spermatids between obstructive azoospermia (OA) patients and non-obstructive azoospermia (NOA) patients. Human spermatogonia, pachytene spermatocytes, and round spermatids from OA patients and NOA patients were isolated using STA-PUT velocity sedimentation and identified by numerous hallmarks for these cells. RNA deep sequencing showed that 396 microRNAs were differentially expressed in human spermatogonia between OA patients and NOA patients and 395 differentially expressed microRNAs were found in human pachytene spermatocytes between OA patients and NOA patients. Moreover, 378 microRNAs were differentially expressed in human round spermatids between OA patients and NOA patients. The differential expression of numerous microRNAs identified by RNA deep sequencing was verified by real-time PCR. Moreover, a number of novel targeting genes for microRNAs were predicted using various kinds of software and further verified by real-time PCR. This study thus sheds novel insights into epigenetic regulation of human normal spermatogenesis and the etiology of azoospermia, and it could offer new targets for molecular therapy to treat male infertility.