生物学杂志 ›› 2025, Vol. 42 ›› Issue (3): 22-.doi: 10.3969/j.issn.2095-1736.2025.03.022

• 研究报告 • 上一篇    下一篇

基于衰老分子标志物的小鼠衰老评估模型的建立及其初步应用

时景景, 何诗丹, 唐雨欣, 周宇荀, 李 凯, 肖君华   

  1. 东华大学 生物与医学工程学院, 上海 201620
  • 出版日期:2025-06-18 发布日期:2025-06-16
  • 通讯作者: 肖君华,教授,研究方向为分子遗传学,E-mail:xiaojunhua@dhu.edu.cn
  • 作者简介:时景景,硕士研究生,研究方向为分子检测,E-mail:19506504976@163.com
  • 基金资助:
    国家重点研发计划项目(2018YFA0801101)

Establishment of a mouse aging assessment model based on molecular markers of aging and its preliminary application

SHI Jingjing, HE Shidan, TANG Yuxin, ZHOU Yuxun, LI Kai, XIAO Junhua   

  1. College of Biological Science and Medical Engineering, Donghua University, Shanghai 201620, China
  • Online:2025-06-18 Published:2025-06-16

摘要: 端粒长度缩短和线粒体DNA拷贝数变化是公认的衰老分子标志物,研究利用定量PCR技术检测端粒长度和线粒体DNA拷贝数在2~24月龄雌、雄C57BL/6小鼠9种组织中的动态变化。通过多元线性回归构建基于两种分子标志物的小鼠衰老评估模型,回归模型的拟合度r2在0.4~0.8。通过该模型发现在雌性或雄性小鼠9种组织中,至少有一种衰老分子标志物与月龄显著性相关。作为实际应用,利用构建的衰老评估模型分析生殖压力是否对雌性衰老产生影响。通过研究发现,生殖加速了雌性衰老的进程,主要体现在外周血、心脏、皮质和脾脏组织。研究构建了9种组织的衰老评估模型,利用该模型可以评估各种实验干预对雌性或雄性C57BL/6小鼠9种组织的衰老加速效应。

关键词: 端粒长度, 线粒体DNA拷贝数, 生殖压力, 衰老评估模型, 荧光定量PCR技术

Abstract: Shortened telomere length and mitochondrial DNA copy number changes are recognized as molecular markers of aging. In this study, quantitative PCR technology was used to detect the dynamic changes of telomere length and mitochondrial DNA copy number in 9 tissues of female and male C57BL/6 mice aged 2-24 months. A mouse aging evaluation model based on two molecular markers was constructed by multiple linear regression, and the fit degree (r2) of the regression model was between 0.4-0.8. Through this model, it was found that at least one molecular marker of senescence was significantly associated with the age of the month in 9 tissues of female or male mice. As a practical application, whether reproductive stress had an effect on female aging was analyzed using the constructed aging assessment model. Studies have found that reproduction accelerates the aging process of the female mice, mainly in peripheral blood, heart, cortical and spleen tissues. In this study, an aging evaluation model was constructed for 9 tissues, which could be used to evaluate the accelerated aging effect of various experimental interventions on 9 tissues of female or male C57BL/6 mice.

Key words: telomere length, mitochondrial DNA copy number, reproductive pressure, aging evaluation model, real-time PCR technology

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