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Effect of microRNA-21 on the proliferation of human degenerated nucleus pulposus by targeting programmed cell death 4
Chen, B; Huang, S G; Ju, L; Li, M; Nie, F F; Zhang, Y; Zhang, Y H; Chen, X; Gao, F.
Afiliação
  • Chen, B; Linyi Second People's Hospital. Department of Orthopedics. Linyi. CN
  • Huang, S G; Linyi Second People's Hospital. Department of Orthopedics. Linyi. CN
  • Ju, L; Linyi Second People's Hospital. Department of Orthopedics. Linyi. CN
  • Li, M; Linyi Second People's Hospital. Department of Orthopedics. Linyi. CN
  • Nie, F F; Linyi Second People's Hospital. Department of Orthopedics. Linyi. CN
  • Zhang, Y; Taishan Medical University. Department of General Surgery. Taian. CN
  • Zhang, Y H; Linyi Second People's Hospital. Department of Orthopedics. Linyi. CN
  • Chen, X; Linyi Second People's Hospital. Department of Orthopedics. Linyi. CN
  • Gao, F; Linyi Second People's Hospital. Department of Orthopedics. Linyi. CN
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;49(6): e5020, 2016. tab, graf
Article em En | LILACS | ID: biblio-951681
Biblioteca responsável: BR1.1
ABSTRACT
This study aims to explore the effect of microRNA-21 (miR-21) on the proliferation of human degenerated nucleus pulposus (NP) by targeting programmed cell death 4 (PDCD4) tumor suppressor. NP tissues were collected from 20 intervertebral disc degeneration (IDD) patients, and from 5 patients with traumatic spine fracture. MiR-21 expressions were tested. NP cells from IDD patients were collected and divided into blank control group, negative control group (transfected with miR-21 negative sequences), miR-21 inhibitor group (transfected with miR-21 inhibitors), miR-21 mimics group (transfected with miR-21 mimics) and PDCD4 siRNA group (transfected with PDCD4 siRNAs). Cell growth was estimated by Cell Counting Kit-8; PDCD4, MMP-2,MMP-9 mRNA expressions were evaluated by qRT-PCR; PDCD4, c-Jun and p-c-Jun expressions were tested using western blot. In IDD patients, the expressions of miR-21 and PDCD4 mRNA were respectively elevated and decreased (both P<0.05). The miR-21 expressions were positively correlated with Pfirrmann grades, but negatively correlated with PDCD4 mRNA (both P<0.001). In miR-21 inhibitor group, cell growth, MMP-2 and MMP-9 mRNA expressions, and p-c-Jun protein expressions were significantly lower, while PDCD4 mRNA and protein expressions were higher than the other groups (all P<0.05). These expressions in the PDCD4 siRNA and miR-21 mimics groups was inverted compared to that in the miR-21 inhibitor group (all P<0.05). MiR-21 could promote the proliferation of human degenerated NP cells by targeting PDCD4, increasing phosphorylation of c-Jun protein, and activating AP-1-dependent transcription of MMPs, indicating that miR-21 may be a crucial biomarker in the pathogenesis of IDD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Assunto principal: Proteínas de Ligação a RNA / MicroRNAs / Proliferação de Células / Proteínas Reguladoras de Apoptose / Núcleo Pulposo Limite: Adult / Aged / Female / Humans / Male Idioma: En Revista: Braz. j. med. biol. res / Rev. bras. pesqui. méd. biol Assunto da revista: BIOLOGIA / MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China País de publicação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Assunto principal: Proteínas de Ligação a RNA / MicroRNAs / Proliferação de Células / Proteínas Reguladoras de Apoptose / Núcleo Pulposo Limite: Adult / Aged / Female / Humans / Male Idioma: En Revista: Braz. j. med. biol. res / Rev. bras. pesqui. méd. biol Assunto da revista: BIOLOGIA / MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China País de publicação: Brasil