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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.
Abstract:
MicroRNAs (miRNAs) are associated with healing or deteriorating degenerated intervertebral disc (IVD) tissues in spinal cord diseases, including intervertebral disc degeneration (IDD). IDD represents a chronic process of extracellular matrix destruction, but the relevant molecular mechanisms implicated in the regenerative effects of miRNAs are unclear. Here, we investigated the regenerative effects of microRNA-140 (miR-140-3p) in an IDD model induced by annulus needle puncture. Bioinformatics analysis was conducted to identify regulatory factors (KLF5/N-cadherin/MDM2/Slug) linked to miR-140-3p effects in IDD. Mesenchymal stem cells (MSCs) were extracted from degenerated IVD nucleus pulposus (NP), and the expression of miR-140-3p/KLF5/N-cadherin/MDM2/Slug was manipulated to explore their effects on cell proliferation, migration, apoptosis and differentiation. The results showed that miR-140-3p was under-expressed in the degenerated IVD NP, whereas its overexpression alleviated IDD. Mechanistic studies suggested that miR-140-3p targeted KLF5 expression, and high KLF5 expression impeded the migration and differentiation of MSCs. In degenerated IVD NP-derived MSCs, MiR-140-3p-mediated KLF5 downregulation simultaneously elevated N-cadherin expression and transcriptionally inhibited MDM2, thus upregulating Slug expression. The experimental data indicated that miR-140-3p enhanced the proliferation, migration and differentiation of degenerated IVD NP-derived MSCs and repressed their apoptosis. The in vivo validation experiment also demonstrated that miR-140-3p inhibited IDD by modulating the KLF5/N-cadherin/MDM2/Slug axis. Collectively, our results uncovered the regenerative role of miR-140-3p in IDD via regulation of the KLF5/N-cadherin/MDM2/Slug axis, which could be a potential therapeutic target for IDD.Abbreviations: miR-140-3p: microRNA-140-3p; IDD: intervertebral disc degeneration; MSCs: Mesenchymal stem cells; IVD: intervertebral disc; MSCs: mesenchymal stem cells; KLF5: Kruppel-like factor 5; MDM2: mouse double minute 2; NC: negative control; DHI: disc height index.
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.
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