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MicroRNA-140-3p alleviates intervertebral disc degeneration via KLF5/N-cadherin/MDM2/Slug axis.
Wang, Zhenyu; Zhang, Shaokun; Zhao, Yuguang; Qu, Zhigang; Zhuang, Xinming; Song, Qingxu; Leng, Jiali; Liu, Yi.
Afiliación
  • Wang Z; Department of Spinal Surgery, The First Hospital of Jilin University, Changchun, P.R. China.
  • Zhang S; Department of Spinal Surgery, The First Hospital of Jilin University, Changchun, P.R. China.
  • Zhao Y; Department of Spinal Surgery, The First Hospital of Jilin University, Changchun, P.R. China.
  • Qu Z; Department of Spinal Surgery, The First Hospital of Jilin University, Changchun, P.R. China.
  • Zhuang X; Department of Spinal Surgery, The First Hospital of Jilin University, Changchun, P.R. China.
  • Song Q; Department of Spinal Surgery, The First Hospital of Jilin University, Changchun, P.R. China.
  • Leng J; Department of Hospice, The First Hospital of Jilin University, Changchun, P.R. China.
  • Liu Y; Department of Spinal Surgery, The First Hospital of Jilin University, Changchun, P.R. China.
RNA Biol ; 18(12): 2247-2260, 2021 12.
Article en En | MEDLINE | ID: mdl-33904383
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Regulación hacia Abajo / Biología Computacional / MicroARNs / Degeneración del Disco Intervertebral / Células Madre Mesenquimatosas Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Animals / Humans / Male Idioma: En Revista: RNA Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2021 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Regulación hacia Abajo / Biología Computacional / MicroARNs / Degeneración del Disco Intervertebral / Células Madre Mesenquimatosas Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Animals / Humans / Male Idioma: En Revista: RNA Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2021 Tipo del documento: Article Pais de publicación: Estados Unidos