Sirt3-mediated mitophagy regulates AGEs-induced BMSCs senescence and senile osteoporosis

Senile osteoporosis (SOP) is widely regarded as one of the typical aging-related diseases due to a decrease in bone mass and the destruction in microarchitecture. The inhibition of mitophagy can promote bone marrow mesenchymal stem cells (BMSCs) senescence, and increasing studies have shown that int...

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Published in:Redox biology 2021-05, Vol.41, p.101915-101915, Article 101915
Main Authors: Guo, Yuanyuan, Jia, Xiong, Cui, Yongzhi, Song, Yu, Wang, Siyuan, Geng, Yongtao, Li, Rui, Gao, Weihang, Fu, Dehao
Format: Article
Language:English
Subjects:
Advanced glycation end products
Aging
Cell senescence
Cellular Senescence
Humans
Mesenchymal Stem Cells
Mitophagy
Osteoporosis
Research Paper
Senile osteoporosis
Sirtuin 3
Sirtuin3
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Summary:Senile osteoporosis (SOP) is widely regarded as one of the typical aging-related diseases due to a decrease in bone mass and the destruction in microarchitecture. The inhibition of mitophagy can promote bone marrow mesenchymal stem cells (BMSCs) senescence, and increasing studies have shown that interventions targeting BMSCs senescence can ameliorate osteoporosis, exhibiting their potential for use as therapeutic strategies. Sirtuin-3 (Sirt3) is an essential mitochondria metabolic regulatory enzyme that plays an important role in mitochondrial homeostasis, but its role in bone homeostasis remains largely unknown. This study seeks to investigate whether advanced glycation end products (AGEs) accumulation aggravated BMSCs senescence and SOP, and explored the mechanisms underlying these effects. We observed that AGEs significantly aggravated BMSCs senescence, as well as promoted mitochondrial dysfunction and inhibited mitophagy in a concentration-dependent manner. In addition, this effect could be further strengthened by Sirt3 silencing. Importantly, we identified that the reduction of Sirt3 expression and the mitophagy were vital mechanisms in AGEs-induced BMSCs senescence. Furthermore, overexpression of Sirt3 by intravenously injection with recombinant adeno-associated virus 9 carrying Sirt3 plasmids (rAAV-Sirt3) significantly alleviated BMSCs senescence and the formation of SOP in SAMP6. In conclusion, our data demonstrated that Sirt3 protects against AGEs-induced BMSCs senescence and SOP. Targeting Sirt3 to improve mitophagy may represent a potential therapeutic strategy for attenuating AGEs-associated SOP.
ISSN:2213-2317
2213-2317
DOI:10.1016/j.redox.2021.101915