Sutovsky Peter, Zelenkova Natalie, Postlerova Pavla, Zigo Michal
Division of Animal Sciences, University of Missouri, Columbia, MO, USA.
Department of Obstetrics, Gynecology and Women's Health, University of Missouri, Columbia, MO, USA.
Adv Exp Med Biol. 2025;1469:273-303. doi: 10.1007/978-3-031-82990-1_12.
In the last two decades, a school of thought emerged that perceives male reproductive health, testicular function, and sperm output as a sentry for general, somatic health. Large-scale epidemiologic studies have already linked the reduced sperm count to increased risk of chronic somatic disease (e.g., cancer, cardiovascular, neurological and bone diseases), yet most of these studies have not taken full advantage of advanced andrological analysis. Altered proteostasis, i.e., the disbalance between protein synthesis and turnover, is a common denominator of many diseases, including but not limited to cancer and neurodegenerative diseases. This chapter introduces the concept of cellular proteostasis as a measure of sperm structural and functional integrity and an endpoint of varied impacts on spermiogenesis and sperm maturation, including heritability, general health, lifestyle, and occupational and environmental reprotoxic exposure. Special consideration is given to small molecule protein modifiers, sperm-binding seminal plasma proteins, zinc-interacting proteins, and redox proteins responsible for the maintenance of protein structure and the protection of spermatozoa from oxidative damage. While the main focus is on human male infertility, serious consideration is given to relevant animal models, and in particular to male food animals with extensive records of fertility from artificial insemination services. Altogether, the proteostatic biomarker discovery and validation studies set the stage for the integration of proteomics of sperm proteostasis with genomic and high throughput phenomic approaches to benefit both human and animal reproductive medicine.
在过去二十年中,出现了一种思想流派,将男性生殖健康、睾丸功能和精子产量视为整体躯体健康的哨兵。大规模流行病学研究已将精子数量减少与慢性躯体疾病(如癌症、心血管疾病、神经疾病和骨骼疾病)风险增加联系起来,但这些研究大多未充分利用先进的男科学分析方法。蛋白质稳态改变,即蛋白质合成与周转之间的失衡,是许多疾病的共同特征,包括但不限于癌症和神经退行性疾病。本章介绍细胞蛋白质稳态的概念,将其作为精子结构和功能完整性的衡量标准,以及对精子发生和精子成熟产生各种影响的终点,这些影响包括遗传因素、总体健康状况、生活方式以及职业和环境中的生殖毒性暴露。特别关注负责维持蛋白质结构以及保护精子免受氧化损伤的小分子蛋白质修饰剂、与精子结合的精浆蛋白、锌相互作用蛋白和氧化还原蛋白。虽然主要关注人类男性不育症,但也认真考虑了相关动物模型,尤其是来自人工授精服务且有丰富生育记录的雄性食用动物。总之,蛋白质稳态生物标志物的发现和验证研究为将精子蛋白质稳态蛋白质组学与基因组学和高通量表型组学方法相结合奠定了基础,以造福人类和动物生殖医学。