卡路里限制如何延缓衰老:表观遗传学视角。

IF 4.8 3区 医学 Q1 GENETICS & HEREDITY Journal of Molecular Medicine-Jmm Pub Date : 2024-05-01 Epub Date: 2024-03-08 DOI:10.1007/s00109-024-02430-y
Gyeong Min Lim, Nagarajan Maharajan, Gwang-Won Cho
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引用次数: 0

摘要

基因组不稳定性和表观遗传学改变是影响衰老的一些重要因素。与年龄相关的异染色质丢失和全基因组 DNA 甲基化减少与基因表达异常有关,从而导致疾病和基因组不稳定。调节这些表观遗传变化对保持基因组完整性至关重要,而控制细胞特性对延缓衰老过程也很重要。大量研究表明,在从啮齿动物到灵长类动物等不同物种中,热量限制是促进长寿和健康衰老的黄金标准。可以推断,通过热量限制等主要效应物延缓衰老涉及细胞特性和表观遗传修饰。因此,通过限制卡路里来了解衰老可能会寻求更深入的理解。在这篇综述中,我们讨论了热量限制如何通过基因组稳定性和表观遗传学改变促进长寿和健康衰老。我们还强调了热量限制的效应物如何参与调节基于染色质的屏障。
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How calorie restriction slows aging: an epigenetic perspective.

Genomic instability and epigenetic alterations are some of the prominent factors affecting aging. Age-related heterochromatin loss and decreased whole-genome DNA methylation are associated with abnormal gene expression, leading to diseases and genomic instability. Modulation of these epigenetic changes is crucial for preserving genomic integrity and controlling cellular identity is important for slowing the aging process. Numerous studies have shown that caloric restriction is the gold standard for promoting longevity and healthy aging in various species ranging from rodents to primates. It can be inferred that delaying of aging through the main effector such as calorie restriction is involved in cellular identity and epigenetic modification. Thus, an understanding of aging through calorie restriction may seek a more in-depth understanding. In this review, we discuss how caloric restriction promotes longevity and healthy aging through genomic stability and epigenetic alterations. We have also highlighted how the effectors of caloric restriction are involved in modulating the chromatin-based barriers.

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来源期刊
Journal of Molecular Medicine-Jmm
Journal of Molecular Medicine-Jmm 医学-医学:研究与实验
CiteScore
9.30
自引率
0.00%
发文量
100
审稿时长
1.3 months
期刊介绍: The Journal of Molecular Medicine publishes original research articles and review articles that range from basic findings in mechanisms of disease pathogenesis to therapy. The focus includes all human diseases, including but not limited to: Aging, angiogenesis, autoimmune diseases as well as other inflammatory diseases, cancer, cardiovascular diseases, development and differentiation, endocrinology, gastrointestinal diseases and hepatology, genetics and epigenetics, hematology, hypoxia research, immunology, infectious diseases, metabolic disorders, neuroscience of diseases, -omics based disease research, regenerative medicine, and stem cell research. Studies solely based on cell lines will not be considered. Studies that are based on model organisms will be considered as long as they are directly relevant to human disease.
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