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转录因子EB(TFEB)是衰老过程及年龄相关疾病的核心调节因子。

TFEB is a central regulator of the aging process and age-related diseases.

作者信息

Abokyi Samuel, Ghartey-Kwansah George, Tse Dennis Yan-Yin

机构信息

School of Optometry, The Hong Kong Polytechnic University, Kowloon, Hong Kong SAR of China; Research Centre for SHARP Vision, The Hong Kong Polytechnic University, Kowloon, Hong Kong SAR of China.

Department of Biomedical Sciences, College of Health and Allied Sciences, University of Cape Coast, Cape Coast, Ghana.

出版信息

Ageing Res Rev. 2023 Aug;89:101985. doi: 10.1016/j.arr.2023.101985. Epub 2023 Jun 14.

Abstract

Old age is associated with a greater burden of disease, including neurodegenerative disorders such as Alzheimer's disease and Parkinson's disease, as well as other chronic diseases. Coincidentally, popular lifestyle interventions, such as caloric restriction, intermittent fasting, and regular exercise, in addition to pharmacological interventions intended to protect against age-related diseases, induce transcription factor EB (TFEB) and autophagy. In this review, we summarize emerging discoveries that point to TFEB activity affecting the hallmarks of aging, including inhibiting DNA damage and epigenetic modifications, inducing autophagy and cell clearance to promote proteostasis, regulating mitochondrial quality control, linking nutrient-sensing to energy metabolism, regulating pro- and anti-inflammatory pathways, inhibiting senescence and promoting cell regenerative capacity. Furthermore, the therapeutic impact of TFEB activation on normal aging and tissue-specific disease development is assessed in the contexts of neurodegeneration and neuroplasticity, stem cell differentiation, immune responses, muscle energy adaptation, adipose tissue browning, hepatic functions, bone remodeling, and cancer. Safe and effective strategies of activating TFEB hold promise as a therapeutic strategy for multiple age-associated diseases and for extending lifespan.

摘要

衰老与更大的疾病负担相关,包括神经退行性疾病,如阿尔茨海默病和帕金森病,以及其他慢性疾病。巧合的是,除了旨在预防与年龄相关疾病的药物干预措施外,流行的生活方式干预措施,如热量限制、间歇性禁食和定期锻炼,会诱导转录因子EB(TFEB)和自噬。在这篇综述中,我们总结了一些新发现,这些发现表明TFEB活性会影响衰老的特征,包括抑制DNA损伤和表观遗传修饰、诱导自噬和细胞清除以促进蛋白质稳态、调节线粒体质量控制、将营养感知与能量代谢联系起来、调节促炎和抗炎途径、抑制衰老并促进细胞再生能力。此外,还在神经退行性变和神经可塑性、干细胞分化、免疫反应、肌肉能量适应、脂肪组织褐变、肝功能、骨重塑和癌症等背景下评估了TFEB激活对正常衰老和组织特异性疾病发展的治疗影响。激活TFEB的安全有效策略有望成为治疗多种与年龄相关疾病和延长寿命的治疗策略。

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