TY - JOUR
T1 - TFEB is a central regulator of the aging process and age-related diseases
AU - Abokyi, Samuel
AU - Ghartey-Kwansah, George
AU - Tse, Yan Yin
N1 - Publisher Copyright:
© 2023 The Authors
PY - 2023/6/14
Y1 - 2023/6/14
N2 - 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.
AB - 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.
KW - Hallmarks of aging
KW - Caloric restriction
KW - Lifespan extension
KW - Senescence
KW - Cell regenerative capacity
KW - Neuroplasticity
UR - http://www.scopus.com/inward/record.url?scp=85162117359&partnerID=8YFLogxK
U2 - 10.1016/j.arr.2023.101985
DO - 10.1016/j.arr.2023.101985
M3 - Journal article
SN - 1568-1637
VL - 89
JO - Ageing Research Reviews
JF - Ageing Research Reviews
M1 - 101985
ER -