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探索睾丸衰老的机制:生物标志物研究进展

Exploring the Mechanisms of Testicular Aging: Advances in Biomarker Research.

作者信息

Chen Wenkang, Zou Hede, Xu Haoran, Cao Rui, Zhang Yapeng, Ma Yongjie, Lin Wei, Zhang Hekun, Zhao Jiayou

机构信息

Graduate School of China Academy of Chinese Medical Sciences, Beijing, China.

Graduate School of Hebei University of Chinese Medicine, Shijiazhuang, China.

出版信息

Aging Dis. 2025 Mar 26. doi: 10.14336/AD.2025.0070.

Abstract

Aging biomarkers quantify aging progression and provide actionable targets for therapeutic interventions to mitigate age-related decline. This review synthesizes emerging evidence on testicular aging biomarkers, focusing on cellular senescence (Leydig, Sertoli, and endothelial cells), protein homeostasis disruption, mitochondrial dysfunction, germ stem cell depletion, sperm telomere length, epigenetic alterations, oxidative stress, inflammation, and gut microbiota dysbiosis. We propose that testicular aging serves as a critical nexus linking reproductive decline with systemic aging processes, with its pathological progression being quantifiable through specific biomarkers including the Leydig, Sertoli, and endothelial cells, INSL3, ribosomal protein RPL39L, sperm telomere length, relative telomere length mitochondrial translocator protein, and sialic acid. By bridging systemic aging paradigms with testis-specific mechanisms, we emphasize the urgency to identify organ-selective biomarkers for targeted interventions, advancing strategies to preserve male fertility and address population aging challenges.

摘要

衰老生物标志物可量化衰老进程,并为减轻与年龄相关衰退的治疗干预提供可操作的靶点。本综述综合了关于睾丸衰老生物标志物的新证据,重点关注细胞衰老(睾丸间质细胞、支持细胞和内皮细胞)、蛋白质稳态破坏、线粒体功能障碍、生殖干细胞耗竭、精子端粒长度、表观遗传改变、氧化应激、炎症和肠道微生物群失调。我们提出,睾丸衰老作为连接生殖功能衰退与全身衰老过程的关键节点,其病理进展可通过特定生物标志物进行量化,包括睾丸间质细胞、支持细胞和内皮细胞、松弛素/胰岛素样肽3(INSL3)、核糖体蛋白RPL39L、精子端粒长度、相对端粒长度、线粒体转位蛋白以及唾液酸。通过将全身衰老范式与睾丸特异性机制相联系,我们强调识别用于靶向干预的器官选择性生物标志物的紧迫性,推进旨在保护男性生育能力和应对人口老龄化挑战的策略。

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