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.

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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