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Published on: July 20, 2022
MiR-125b-1-3p-mediated UQCRB inhibition facilitates mitochondrial metabolism disorders in a rat cellular
Sha Lu1, Cong'e Tan1, Xue Xiao1
1College of Basic Medicine, Shaanxi University of Chinese Medicine, Xianyang, Shaanxi, China.
Backgroud:
Cellular senescence is closely related to human aging and multiple aging-related diseases, and impaired mitochondrial energy metabolism is an important mechanism of cellular senescence. Notably, microRNA-125b-1-3p (miR-125b-1-3p) is a microRNA (miR, miRNA) that may be associated with mitochondrial energy metabolism. Ubiquinol-cytochrome c reductase binding protein (UQCRB) gene, predicted by bioinformatics tools to be targeted by miR-125b-1-3p, could serve as a novel diagnostic indicator and therapeutic target for cellular senescence-associated diseases, as well as a new idea for delaying aging.
Methods:
First, the dual-luciferase reporter gene assay was used to identify UQCRB as a target gene of miR-125b-1-3p. Next, miRNA interference technology was conducted to verify that miR-125b-1-3p could negatively regulate the expression of UQCRB. Subsequently, the influence of miR-125b-1-3p on mitochondrial energy metabolism function was explored by observing the internal substances and ultrastructure of mitochondria. Further, an in vitro model of cellular senescence was established in rat renal tubular epithelial cells, which was characterized by detecting senescence-related proteins p16 and p21 and beta-galactosidase (β-gal) activity. Finally, the mitochondrial energy metabolism function of hydrogen peroxide (H2O2)-incubated cells was explored.
Results:
The experimental results revealed that miR-125b-1-3p affected the mitochondrial energy metabolism function by inhibiting the target gene UQCRB. Meanwhile, the level of mitochondrial energy metabolism function in H2O2-incubated senescent cells was lower than that in normal cells.
Conclusion:
In this study, we identified the target gene, UQCRB, of miR-125b-1-3p, and demonstrated its role in the pathway of mitochondrial energy metabolism, as well as its possible effect on cellular senescence through this pathway. The ameliorative effects on cellular senescence can be further explored in subsequent studies to provide additional options for delaying aging or treating aging-related diseases.
Insights
MicroRNA-125b-1-3p regulates mitochondrial energy metabolism by inhibiting the UQCRB gene, offering potential therapeutic targets for cellular senescence and aging-related diseases.
Area of Science:
- Cellular and Molecular Biology
- Aging Research
- Mitochondrial Biology
Background:
- Cellular senescence is linked to aging and age-related diseases, with impaired mitochondrial energy metabolism as a key mechanism.
- MicroRNA-125b-1-3p (miR-125b-1-3p) is implicated in mitochondrial energy metabolism.
- The Ubiquinol-cytochrome c reductase binding protein (UQCRB) gene is a predicted target of miR-125b-1-3p and a potential biomarker for senescence.
Purpose of the Study:
- To investigate the regulatory role of miR-125b-1-3p in mitochondrial energy metabolism.
- To confirm UQCRB as a direct target of miR-125b-1-3p.
- To explore the potential of this pathway in cellular senescence and aging.
Main Methods:
- Dual-luciferase reporter gene assay to identify UQCRB as a miR-125b-1-3p target.
- MiRNA interference to assess the regulatory effect of miR-125b-1-3p on UQCRB expression.
- Analysis of mitochondrial function and senescence markers in vitro models.
Main Results:
- miR-125b-1-3p was confirmed to inhibit UQCRB expression, impacting mitochondrial energy metabolism.
- Senescent cells induced by hydrogen peroxide (H2O2) exhibited reduced mitochondrial energy metabolism compared to normal cells.
Conclusions:
- miR-125b-1-3p regulates mitochondrial energy metabolism via the UQCRB gene.
- This pathway plays a role in cellular senescence.
- Targeting miR-125b-1-3p and UQCRB may offer strategies for delaying aging and treating senescence-associated diseases.
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