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MicroRNA-126 attenuates palmitate-induced apoptosis by targeting TRAF7 in HUVECs.
Wang, Yi; Wang, Feng; Wu, Yan; Zuo, Li; Zhang, Sumei; Zhou, Qing; Wei, Wei; Wang, Yuan; Zhu, Huaqing.
Afiliación
  • Wang Y; Institute of Clinical Pharmacology, Anhui Medical University, Hefei, 230032, Anhui, People's Republic of China.
Mol Cell Biochem ; 399(1-2): 123-30, 2015 Jan.
Article en En | MEDLINE | ID: mdl-25318608
ABSTRACT
The aim of the present study was to explore the role of miR-126 in palmitate-induced HUVECs apoptosis and the possible mechanisms. Palmitate inhibited miR-126 expression in HUVECs, increased reactive oxygen species (ROS) production, and induced apoptosis as determined by up-regulation of caspase-3 activity and DNA fragmentation. Overexpression of miR-126 decreased ROS production, TNF-α expression, and apoptosis in palmitate-stimulated HUVECs. In contrast, miR-126 antagomir enhanced palmitate-induced ROS production, TNF-α expression, and apoptosis. The induction of miR-126 correlated with a reduction in TRAF7. We further showed that miR-126 targeted and inhibited TRAF7 expression through target sites located in the 3' untranslated region of TRAF7 mRNA. In concordance, miR-126 mimic reduced TRAF7 protein in HUVECs, whereas the inhibition of miR-126 increased it. This study demonstrates an anti-apoptotic role of miR-126 in HUVECs and identifies TRAF7 as a direct target of miR-126 in HUVECs.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Palmitatos / Apoptosis / MicroARNs / Péptidos y Proteínas Asociados a Receptores de Factores de Necrosis Tumoral / Células Endoteliales de la Vena Umbilical Humana Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Mol Cell Biochem Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Palmitatos / Apoptosis / MicroARNs / Péptidos y Proteínas Asociados a Receptores de Factores de Necrosis Tumoral / Células Endoteliales de la Vena Umbilical Humana Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Mol Cell Biochem Año: 2015 Tipo del documento: Article