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Updated: Sep 26, 2025

Calcification of Vascular Smooth Muscle Cells and Imaging of Aortic Calcification and Inflammation
Published on: May 31, 2016
MiR-708-5p/Pit-1 axis mediates high phosphate-induced calcification in vascular smooth muscle cells via
Na Wu1, Guo-Bing Liu1, Yu-Min Zhang1
1Department of Cardiology, The Third Hospital of Changsha, Changsha, China.
Abstract:
Recently, the underlying mechanism of vascular calcification (VC) has been partially elucidated. However, it is still high incidence, and no effective treatment has been found. This study aims at figuring out the underlying mechanisms of microRNA-708-5p (miR-708-5p)/sodium-phosphate transporter 1 (Pit-1) axis in high phosphate (HP)-induced VC of T/G HA-VSMCs. Alizarin Red S staining was used to evaluate calcium salt deposition, and the activity of alkaline phosphatase (ALP) was determined by measuring the absorbance at 405 nm. RT-qPCR and Western blot were performed to assess the levels of miR-708-5p and Pit-1, the levels of ALP, Pit-1, β-catenin, glycogen synthesis kinase 3 β (GSK3β), and p-GSK3β proteins, respectively. The interaction between miR-708-5p and Pit-1 was validated by luciferase reporter assay. Our findings illustrated that miR-708-5p was downregulated and Pit-1was upregulated in HP-induced VC. MiR-708-5p mimics inhibited HP-induced VC. Further experiments demonstrated that miR-708-5p targets Pit-1. In addition, miR-708-5p inactivates the Wnt8b/β-catenin pathway via targeting Pit-1 to reduce HP-induced VC. MiR-708-5p has a crucial effect on VC via targeting Pit-1 and inhibiting Wnt8b/β-catenin pathway, it may serve as a new target for VC treatment.
Insights
MicroRNA-708-5p (miR-708-5p) targets Pit-1, inhibiting the Wnt8b/β-catenin pathway. This mechanism reduces high phosphate-induced vascular calcification (VC), suggesting miR-708-5p as a potential therapeutic target for VC.
Area of Science:
- Cardiovascular Biology
- Molecular Medicine
- Biochemistry
Background:
- Vascular calcification (VC) remains a prevalent condition with limited treatment options.
- Understanding the molecular mechanisms driving VC is crucial for developing effective therapies.
Purpose of the Study:
- To investigate the role of the microRNA-708-5p (miR-708-5p)/sodium-phosphate transporter 1 (Pit-1) axis in high phosphate-induced VC.
- To elucidate the underlying molecular pathways involved in this process.
Main Methods:
- Assessed calcium deposition using Alizarin Red S staining and alkaline phosphatase (ALP) activity.
- Quantified miR-708-5p and Pit-1 levels via RT-qPCR and Western blot.
- Validated miR-708-5p and Pit-1 interaction using luciferase reporter assays.
Main Results:
- miR-708-5p was downregulated, while Pit-1 was upregulated in high phosphate-induced VC.
- miR-708-5p mimics significantly inhibited high phosphate-induced VC.
- miR-708-5p directly targets Pit-1, inactivating the Wnt8b/β-catenin pathway.
Conclusions:
- miR-708-5p plays a critical role in regulating vascular calcification by targeting Pit-1 and inhibiting the Wnt8b/β-catenin pathway.
- The miR-708-5p/Pit-1 axis presents a promising novel therapeutic target for vascular calcification treatment.
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