与凋亡相关的 MiRNA 与冻融过程后无精子荷斯坦公牛的功能和流式细胞仪参数的关系

IF 1.6 4区 生物学
Biopreservation and Biobanking Pub Date : 2024-12-01 Epub Date: 2024-04-30 DOI:10.1089/bio.2023.0135
Morteza Taravat, Amirmahdi Roshanzamir, Maryam Rahbar, Tohid Rezaei Topraggaleh, Reza Asadpour, Mustafa Numan Bucak
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引用次数: 0

摘要

精子中的许多细胞过程,包括凋亡和活力,都受 miRNA 的调控。无精子症(AS)被认为是精子活力下降导致不育的原因之一,而不同的 miRNA 和分子通路参与了无精子症的发生。研究人员采用了四头患有正常无精子症(NS)、总活力≥70%、进行性活力≥60%的荷斯坦公牛的 32 份精液样本,以及四头患有 AS、总活力≤40%、进行性活力≤32%的公牛的 32 份精液样本,以研究 AS 组中与细胞凋亡相关的 miRNA 的功能。样本经三聚氰胺-蛋黄扩展剂稀释后吸入0.5 mL吸管,在-196°C下冷冻。冷冻后,精液样本在 37°C 下解冻 2 周,并对精子运动参数、质膜完整性、顶体完整性、DNA 断裂、凋亡状态以及与凋亡相关的 miRNA(miR-2114、miR-296-3p、miR-455-3p 和 miR345-3p)的表达进行评估。结果表明,NS组的功能和流式细胞术参数明显优于AS组。与AS组相比,NS组的miR-455-3pp和miR-2412上调,而miR-345-3p下调。在AS组中,miR-296-39、miR-2412和miR-345-3p水平与膜完整性、DNA片段和凋亡状态密切相关。研究结果表明,根据生物信息学分析在AS和NS样本中筛选出的miRNA与功能和流式细胞术指标有很大的关联,可能参与了AS样本中细胞凋亡和运动的调控。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Apoptotic-Related MiRNAs Correlated with Functional and Flow Cytometric Parameters in Asthenozoospermic Holstein Bulls After Freeze-Thaw Process.

Many cellular processes in spermatozoa, including apoptosis and motility, are regulated by miRNA. Different miRNAs and molecular pathways are involved in asthenozoospermia (AS) conditions, which are thought to be one of the causes of infertility with reduced sperm motility. Thirty-two semen samples from four Holstein bulls with normozoospermia (NS), total motility ≥ 70%, and progressive motility ≥ 60%, and 32 semen samples from four bulls with AS, total motility ≤ 40%, and progressive motility ≤ 32% were used to investigate the function of apoptosis-related miRNAs in the AS group. Samples were then aspirated into a 0.5 mL straw after dilution with a Tris-egg yolk extender and frozen at -196°C. After freezing, semen samples were thawed for 2 weeks at 37°C and sperm kinematic parameters, plasma membrane integrity, acrosome integrity, DNA fragmentation, apoptosis status, and expression of apoptosis-related miRNAs (miR-2114, miR-296-3p, miR-455-3p, and miR345-3p) were evaluated. Our results showed that the functional and flow cytometric parameters of the NS group were significantly better than those of the AS group. In the NS group, miR-455-3pp and miR-2412 were upregulated, while miR-345-3p was downregulated compared with the AS group. In the AS group, miR-296-39, miR-2412, and miR-345-3p levels were strongly correlated with membrane integrity, DNA fragmentation, and apoptosis status. The findings demonstrated that the selected miRNAs based on bioinformatic analysis in AS and NS samples had a substantial association with functional and flow cytometry indicators and may be involved in regulating apoptosis and motility in AS samples.

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来源期刊
Biopreservation and Biobanking
Biopreservation and Biobanking Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
自引率
12.50%
发文量
114
期刊介绍: Biopreservation and Biobanking is the first journal to provide a unifying forum for the peer-reviewed communication of recent advances in the emerging and evolving field of biospecimen procurement, processing, preservation and banking, distribution, and use. The Journal publishes a range of original articles focusing on current challenges and problems in biopreservation, and advances in methods to address these issues related to the processing of macromolecules, cells, and tissues for research. In a new section dedicated to Emerging Markets and Technologies, the Journal highlights the emergence of new markets and technologies that are either adopting or disrupting the biobank framework as they imprint on society. The solutions presented here are anticipated to help drive innovation within the biobank community. Biopreservation and Biobanking also explores the ethical, legal, and societal considerations surrounding biobanking and biorepository operation. Ideas and practical solutions relevant to improved quality, efficiency, and sustainability of repositories, and relating to their management, operation and oversight are discussed as well.
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