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Updated: Nov 12, 2025

Techniques to Induce and Quantify Cellular Senescence
Published on: May 1, 2017
Caffeine promotes the expression of telomerase reverse transcriptase to regulate cellular senescence and aging
Li Tao1, Wei Zhang, Yaxin Zhang
1School of Biotechnology, Tianjin University of Science and Technology, Key Lab of Industrial Fermentation Microbiology of the Ministry of Education, State Key Laboratory of Food Nutrition and Safety, Tianjin 300457, China. diaoaipo@tust.edu.cn liyuyin@tust.edu.cn.
Caffeine extends telomere length by promoting telomerase reverse transcriptase (TERT) expression, thereby delaying cellular senescence and aging. This finding explains health benefits associated with caffeine consumption.
Area of Science:
- Cellular and Molecular Biology
- Gerontology
- Nutritional Science
Background:
- Telomere shortening is a key driver of cellular senescence and aging.
- Caffeine, a common stimulant in coffee and tea, has potential health benefits.
- The molecular mechanisms underlying caffeine's anti-aging effects require further investigation.
Purpose of the Study:
- To investigate the effect of caffeine on telomere length and cellular senescence.
- To elucidate the role of telomerase reverse transcriptase (TERT) in caffeine's action.
- To evaluate caffeine's impact on age-related organ changes in animal models.
Main Methods:
- In vitro studies measuring TERT expression (mRNA and protein) and telomere length.
- TERT knockdown experiments to assess its necessity for caffeine's effects.
- In vivo studies involving long-term caffeine administration to mice.
- Analysis of organ indices and histological changes in aged mice.
Main Results:
- Caffeine significantly increased TERT expression at both mRNA and protein levels.
- Caffeine treatment led to telomere elongation and prevention of cellular senescence.
- TERT knockdown abolished caffeine-induced telomere extension.
- Long-term caffeine administration in mice increased TERT expression and telomere length in thymus and spleen.
- Caffeine improved organ indices and reversed age-related histological damage in thymus, spleen, and liver.
Conclusions:
- Caffeine promotes TERT expression, leading to telomere elongation and delayed cellular senescence.
- Caffeine's ability to counteract age-related organ decline suggests a significant role in mitigating aging processes.
- These findings provide a molecular basis for the health benefits of caffeine-containing foods.
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