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MicroRNA-124 inhibits TNF-α- and IL-6-induced osteoclastogenesis.
Ohnuma, Kenichiro; Kasagi, Shimpei; Uto, Kenichi; Noguchi, Yoriko; Nakamachi, Yuji; Saegusa, Jun; Kawano, Seiji.
Afiliação
  • Ohnuma K; Division of Laboratory Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Kasagi S; Department of Clinical Laboratory, Kobe University Hospital, Kobe, Japan.
  • Uto K; Division of Laboratory Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Noguchi Y; Department of Clinical Laboratory, Kobe University Hospital, Kobe, Japan.
  • Nakamachi Y; Department of Clinical Laboratory, Kobe University Hospital, Kobe, Japan.
  • Saegusa J; Department of Clinical Laboratory, Kobe University Hospital, Kobe, Japan.
  • Kawano S; Department of Clinical Laboratory, Kobe University Hospital, Kobe, Japan.
Rheumatol Int ; 39(4): 689-695, 2019 04.
Article em En | MEDLINE | ID: mdl-30547186
ABSTRACT
Receptor activator for nuclear factor κB ligand (RANKL)-independent osteoclastogenic pathway was reported recently. MicroRNA (miR)-124 has been known to suppress RANKL-dependent osteoclastogenesis by inhibiting NFATc1 expression. However, whether miR-124 regulates a RANKL-independent pathway has not been elucidated. In this study, we examined whether a RANKL-independent pathway is regulated by miR-124 in addition to the RANKL-dependent one. Using osteoclastogenic culture and pit-formation assay, we found that a miR-124 mimic inhibited osteoclastogenesis in mouse bone marrow-derived macrophages stimulated by TNF-α, IL-6, and M-CSF in the presence of osteoprotegerin. We also showed that the expression levels of osteoclast-specific genes and NFATc1 protein were suppressed in the miR-124 mimic-transfected cells by performing quantitative-polymerase chain reaction and western blotting. Our results indicate that miR-124 is important in inhibiting both RANKL-dependent and -independent osteoclast differentiation by suppressing NFATc1-mediated pathway.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteogênese / MicroRNAs / Macrófagos Limite: Animals Idioma: En Revista: Rheumatol Int Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteogênese / MicroRNAs / Macrófagos Limite: Animals Idioma: En Revista: Rheumatol Int Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Japão