Low acrosin activity is associated with decreased Spam1/acrosin expression and GSH deficiency-caused premature acrosome release of human sperm cells.

IF 3.2 3区 生物学 Q3 CELL BIOLOGY
Cell and Tissue Research Pub Date : 2023-12-01 Epub Date: 2023-10-14 DOI:10.1007/s00441-023-03826-x
Mengyuan Lin, Pengyun Ling, Qingwen He, Daozhen Chen, Lianshuai Zheng, Lisha Tang, Shi-Wen Jiang
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Abstract

Low acrosin activity (LAA) is associated with sperm function anomaly and poor outcomes of in vitro fertilization. In this study, we confirm that 993 semen samples with LAA had a reduced sperm motility and low in vitro fertilization rate in comparison with 1332 normal controls (NC). Proteomic comparison between 11 LAA and 11 NC sperm samples identified 35 upregulated and 99 downregulated proteins in the LAA group. Indeed, proteomic data showed that acrosome enzymes Spam1 and Acrosin were among the downregulated proteins in the LAA group, which was validated by quantitative PCR and immunefluorescent staining of sperm cells. The KEEG pathway analysis revealed a deficiency of GSH and Gln biosynthesis in LAA sperm cells. Immunofluorescent staining of sperms and quantitative PCR verified downregulation of GLUL and GCLC, the key enzymes for GSH and Gln biosynthesis. Moreover, the results of ELISA assay confirmed low levels of GSH and Gln in LAA sperm cells. Mechanistic studies showed that addition of 10 mM H2O2 to semen samples led to a significant reduction of acrosin activity and sperm motility, most possibly by triggering premature acrosome release. In contrast, the presence of 20 mM GSH blocked the oxidative effects of H2O2. Since GSH counteracts the oxidative stress and Gln participates in TCA cycling, their deficiency may affect the redox balance as well as energy production of sperm cells. These findings shed new light on the pathological mechanisms of infertility associated with LAA. Male infertility patients could benefit from GSH supplement by improvement of acrosin activity and other sperm functions.

Abstract Image

顶体蛋白酶活性低与Spam1/顶体蛋白酶表达降低和GSH缺乏导致人类精子细胞顶体过早释放有关。
顶体酶活性低与精子功能异常和体外受精不良有关。在这项研究中,我们证实,与1332名正常对照组(NC)相比,993份LAA精液样本的精子活力降低,体外受精率较低。11个LAA和11个NC精子样本之间的蛋白质组学比较在LAA组中鉴定出35个上调蛋白和99个下调蛋白。事实上,蛋白质组学数据显示,顶体酶Spam1和Acrosin是LAA组中下调的蛋白质之一,这一点通过定量PCR和精子细胞免疫荧光染色得到了验证。KEEG通路分析显示LAA精子细胞中GSH和Gln生物合成缺乏。精子的免疫荧光染色和定量PCR证实了谷胱甘肽和谷氨酰胺生物合成的关键酶GLUL和GCLC的下调。此外,ELISA测定结果证实LAA精子细胞中GSH和Gln水平较低。机制研究表明,向精液样本中添加10mM H2O2会导致顶体蛋白酶活性和精子活力显著降低,最有可能是通过触发顶体过早释放。相反,20mM GSH的存在阻断了H2O2的氧化作用。由于GSH可以对抗氧化应激,Gln参与TCA循环,它们的缺乏可能会影响精子细胞的氧化还原平衡和能量产生。这些发现为LAA相关不孕的病理机制提供了新的线索。男性不育患者可通过提高顶体酶活性和其他精子功能而从补充谷胱甘肽中获益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell and Tissue Research
Cell and Tissue Research 生物-细胞生物学
CiteScore
7.00
自引率
2.80%
发文量
142
审稿时长
1 months
期刊介绍: The journal publishes regular articles and reviews in the areas of molecular, cell, and supracellular biology. In particular, the journal intends to provide a forum for publishing data that analyze the supracellular, integrative actions of gene products and their impact on the formation of tissue structure and function. Submission of papers with an emphasis on structure-function relationships as revealed by recombinant molecular technologies is especially encouraged. Areas of research with a long-standing tradition of publishing in Cell & Tissue Research include: - neurobiology - neuroendocrinology - endocrinology - reproductive biology - skeletal and immune systems - development - stem cells - muscle biology.
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