MicroRNA-140-3p alleviates intervertebral disc degeneration via KLF5/N-cadherin/MDM2/Slug axis

Zhenyu Wang1, Shaokun Zhang1, Yuguang Zhao1

  • 1Department of Spinal Surgery, The First Hospital of Jilin University, Changchun, P.R. China.

RNA Biology
|April 27, 2021
PubMed

Insights

MicroRNA-140-3p (miR-140-3p) overexpression alleviates intervertebral disc degeneration (IDD) by promoting mesenchymal stem cell (MSC) regeneration. This study reveals miR-140-3p

Area of Science:

  • Biomedical research
  • Molecular biology
  • Regenerative medicine

Background:

  • Intervertebral disc degeneration (IDD) involves extracellular matrix destruction, with unclear miRNA roles.
  • MicroRNAs (miRNAs) influence tissue healing or deterioration in spinal cord diseases like IDD.

Purpose of the Study:

  • Investigate the regenerative effects of microRNA-140-3p (miR-140-3p) in an IDD model.
  • Elucidate the molecular mechanisms underlying miR-140-3p's role in IDD.
  • Identify potential therapeutic targets for IDD.

Main Methods:

  • Induced an IDD model via annulus needle puncture.
  • Performed bioinformatics analysis to identify regulatory factors (KLF5/N-cadherin/MDM2/Slug).
  • Extracted and manipulated mesenchymal stem cells (MSCs) from degenerated nucleus pulposus (NP) to assess miR-140-3p effects on cell functions.

Main Results:

  • miR-140-3p was underexpressed in degenerated IVD NP; its overexpression alleviated IDD.
  • miR-140-3p targeted KLF5, inhibiting MSC migration and differentiation.
  • miR-140-3p enhanced MSC proliferation, migration, and differentiation while repressing apoptosis by modulating the KLF5/N-cadherin/MDM2/Slug axis.

Conclusions:

  • miR-140-3p demonstrates a regenerative role in IDD.
  • The KLF5/N-cadherin/MDM2/Slug axis is a key pathway regulated by miR-140-3p in IDD.
  • miR-140-3p represents a potential therapeutic target for IDD treatment.