Reza Emad, Azizi Hossein, Skutella Thomas
Faculty of Biotechnology, Amol University of Special Modern Technologies, Amol, Iran.
Institute for Anatomy and Cell Biology, Medical Faculty, University of Heidelberg, Germany.
Ann Anat. 2025 Apr;259:152391. doi: 10.1016/j.aanat.2025.152391. Epub 2025 Feb 11.
In order to sustain reproduction, this study aims to investigate the role of N-Myc in the regulation of spermatogonial stem cell differentiation and the consequent generation of sperm during spermatogenesis. By analyzing specific gene expression patterns associated with N-Myc signaling pathways, we seek to identify potential targets for infertility treatments.
In this study on mice, we constructed a PPI network in embryonic stem cells, germ cells, SSCs and pluripotent stem cells using the GEO datasets, NCBI, STRING, and Cytoscape databases. Then, after isolating spermatogonial stem cells from 6 C57BL/6 mice, ES-like cells were prepared. We further examined N-Myc, Oct4, Sox9, Vasa, and Plzf expression in testes, SSCs, and ES-like cells by immunohistochemistry (IHC) and immunocytochemistry (ICC), also the expression of N-Myc using RT-PCR. Finally, we performed gene set enrichment and miRNA analysis for N-Myc using Enrichr and miRTarBase.
N-Myc has a central role in PPIs for genes maintaining pluripotency. In addition, this gene is coexpressed with Oct4, and positive expression of the Vasa and Plzf genes was observed in seminiferous tubule cells. The interaction network of N-Myc with microRNAs and lncRNAs was constructed, and the biological roles of N-Myc in spermatogenesis, such as glycolysis, were revealed.
The result highlight that N-Myc is essential for orchestrating the differentiation of spermatogonial stem cells into mature sperm by interacting with key regulatory factors. This underscores its pivotal role in both maintaining pluripotency and facilitating successful spermatogenesis, which may inform future strategies for addressing infertility.
为了维持生殖,本研究旨在探讨N-Myc在精子发生过程中对精原干细胞分化及随后精子生成的调控作用。通过分析与N-Myc信号通路相关的特定基因表达模式,我们试图确定不孕症治疗的潜在靶点。
在本项针对小鼠的研究中,我们利用GEO数据集、NCBI、STRING和Cytoscape数据库,在胚胎干细胞、生殖细胞、精原干细胞和多能干细胞中构建了蛋白质-蛋白质相互作用(PPI)网络。然后,从6只C57BL/6小鼠中分离出精原干细胞后,制备了类胚胎干细胞。我们通过免疫组织化学(IHC)和免疫细胞化学(ICC)进一步检测了睾丸、精原干细胞和类胚胎干细胞中N-Myc、Oct4、Sox9、Vasa和Plzf的表达,同时利用逆转录聚合酶链反应(RT-PCR)检测了N-Myc的表达。最后,我们使用Enrichr和miRTarBase对N-Myc进行了基因集富集和微小RNA(miRNA)分析。
N-Myc在维持多能性基因的PPI中起核心作用。此外,该基因与Oct4共表达,在生精小管细胞中观察到Vasa和Plzf基因呈阳性表达。构建了N-Myc与miRNA和长链非编码RNA(lncRNA)的相互作用网络,并揭示了N-Myc在精子发生中的生物学作用,如糖酵解。
结果表明,N-Myc通过与关键调控因子相互作用,对于协调精原干细胞分化为成熟精子至关重要。这突出了其在维持多能性和促进成功精子发生中的关键作用,这可能为未来解决不孕症的策略提供参考。