Panahi Alireza, Mirza Ahmadi Sina, Asaadi Tehrani Golnaz
Department of the Genetics, Zanjan Branch, Islamic Azad University, Zanjan, Iran.
Department of the Genetics, Zanjan Branch, Islamic Azad University, Zanjan, Iran. Email:
Int J Fertil Steril. 2022 Apr;16(2):122-127. doi: 10.22074/IJFS.2021.138190.1029. Epub 2022 May 8.
Improving sperm motility results in increasing the success of a treatment cycle. Recently, sperm RNA has been used for diagnostic purposes such as whole seminal fluid, sperm analysis, and sperm quality test in patients undergoing fertilization/intracytoplasmic sperm injection (IVF/ICSI). SPATA18-P53 pathway is considered an essential pathway related to sperm mitochondria, which controls mitochondrial quality by eliminating its oxidative proteins. Oxidative stress may decrease sperm motility and affect sperm quality negatively due to an increase in P53 expression. SPATA18 protein is found in satellite fibers related to outer dense fibers in the middle piece of sperm. The downregulation of SPATA18 in the asthenospermia group can represent this gene's critical function in sperm motility and fertility. The present study aimed to assess the relationship between and gene expression in sperm cells obtained from normospermia and asthenospermia.
In this case-control study, the quantitative real-time polymerase chain reaction (RT-PCR) technique was used to measure the and gene expression level in sperm samples collected from 21 patients and 63 healthy individuals. Further, the sperm DNA fragmentation assay (SDFA) kit was applied to determine the relative apoptosis level in cells and evaluate the biochemical information related to the patients' sperm samples. Furthermore, all the participants completed the consent form, and the ethics committee confirmed the study.
Based on the results, the and gene expression levels in most of the samples, in which motility was less than 40%, increased and decreased (P≤0.001), respectively.
The and gene expression levels increased and decreased in the asthenospermic patients, respectively, compared to the control group. Thus, the and expression levels can be used as an appropriate marker for diagnosing sperm motility in males.
提高精子活力可提高治疗周期的成功率。最近,精子RNA已被用于诊断目的,如对接受体外受精/卵胞浆内单精子注射(IVF/ICSI)的患者进行全精液、精子分析和精子质量检测。SPATA18-P53通路被认为是与精子线粒体相关的重要通路,它通过清除线粒体的氧化蛋白来控制线粒体质量。氧化应激可能会降低精子活力,并由于P53表达增加而对精子质量产生负面影响。SPATA18蛋白存在于精子中段与外致密纤维相关的卫星纤维中。弱精子症组中SPATA18的下调可表明该基因在精子活力和生育能力中的关键作用。本研究旨在评估正常精子症和弱精子症患者精子细胞中[具体基因名称未给出]和[具体基因名称未给出]基因表达之间的关系。
在这项病例对照研究中,采用定量实时聚合酶链反应(RT-PCR)技术测量从21例患者和63名健康个体收集的精子样本中[具体基因名称未给出]和[具体基因名称未给出]基因的表达水平。此外,应用精子DNA碎片化分析(SDFA)试剂盒来确定细胞中的相对凋亡水平,并评估与患者精子样本相关的生化信息。此外,所有参与者均签署了知情同意书,伦理委员会批准了该研究。
根据结果,在大多数活力低于40%的样本中,[具体基因名称未给出]和[具体基因名称未给出]基因表达水平分别升高和降低(P≤0.001)。
与对照组相比,弱精子症患者中[具体基因名称未给出]和[具体基因名称未给出]基因表达水平分别升高和降低。因此,[具体基因名称未给出]和[具体基因名称未给出]的表达水平可作为诊断男性精子活力的合适标志物。