1. 弱精子症精子中 miRNAs 特异表达及潜在致病靶点的分析.
- Author
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汤 莹, 唐敏英, 张湧波, 郑美玉, 林炎鸿, 吴丹红, and 路 君
- Abstract
Asthenozoospermia, a condition observed in 40% of infertile males, is characterized by reshiced sperm mastility. MicroRNAs (miRNAs) play a pivotal role in spermatogenesis, yet their involvement in asthenozoospermia remains poorly understood. This study aims to elucidate the molecular mechanisms of miRNAs in asthenospermia. Method (): Sperm samples wer collected from individuals with severe asthenozoospermia and healthy males. High-throughput sequencing was employed to identify differentially expressed miRNAs., followed by bioinformatics analysis of these significant miRNAs. The ahered expression of two specific miRNAs and their target genes was confirmed using qRT-PCR. Rasult(): When comparing severe asthenozoospermia patients to healthy males, 146 miRNAs exhibited significam alterations (0.05; log2 Fold Change>1), with 52 upregulated and 94 downregulated miRNAs. The ten most significantly upregidated and downregulated miRNAs were subjected to target gene prediction through the miRDB and TargetScan databases, a total of 1407 target genes were found to be supported by both databases. Enrichment analysis revealed that miRNA target genes were enriched in sperm cell processes, and they wem involved in oxidative metabolism, stimadus response, proliferation, differentiation, and apoptosis in sperm cells. Pathway analysis indicated that target genes might participate in processes such as autophagy, cellular senescence, the PIK-Akt signaling pathway, the MAPK signaling pathway, the HIF-1 signaling pathway, and the mTOR signaling pathway Notably, ansing the specifically upwegıdated miRNAs in ast henazoospermia, haa-miR-371-5p-and haa-miR-2355-5p were identified, with their respective target genes being the autophagy effector protein Berlin! and matochondrial inner membrane protein prohibain2 (PHB2), both directly involved in mutochondrial autophagy. qRT-PCR results demonstrated an increused expression of haa-mik-371a-5p and hsa-miR-2355-5p in sperm as motility declined. Conclusion(s): This study identified miRNAs with specific dysregulation in the sperm of asthenozoospermia patients and their target genes, offering new insights and a theoretical basis for further investigation into the mechanisms by which miRNAs regulate mitochondrial autophagic functions inlow motility sperm. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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