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J Immunol ; 204(9): 2392-2400, 2020 05 01.
Artículo en Inglés | MEDLINE | ID: mdl-32213561

RESUMEN

Deregulation of mRNA translation engenders many human disorders, including obesity, neurodegenerative diseases, and cancer, and is associated with pathogen infections. The role of eIF4E-dependent translational control in macrophage inflammatory responses in vivo is largely unexplored. In this study, we investigated the involvement of the translation inhibitors eIF4E-binding proteins (4E-BPs) in the regulation of macrophage inflammatory responses in vitro and in vivo. We show that the lack of 4E-BPs exacerbates inflammatory polarization of bone marrow-derived macrophages and that 4E-BP-null adipose tissue macrophages display enhanced inflammatory gene expression following exposure to a high-fat diet (HFD). The exaggerated inflammatory response in HFD-fed 4E-BP-null mice coincides with significantly higher weight gain, higher Irf8 mRNA translation, and increased expression of IRF8 in adipose tissue compared with wild-type mice. Thus, 4E-BP-dependent translational control limits, in part, the proinflammatory response during HFD. These data underscore the activity of the 4E-BP-IRF8 axis as a paramount regulatory mechanism of proinflammatory responses in adipose tissue macrophages.


Asunto(s)
Proteínas Adaptadoras Transductoras de Señales/genética , Tejido Adiposo/metabolismo , Inflamación/genética , Factores Reguladores del Interferón/genética , Macrófagos/metabolismo , Biosíntesis de Proteínas/genética , Animales , Médula Ósea/metabolismo , Dieta Alta en Grasa/métodos , Factor 4E Eucariótico de Iniciación/genética , Expresión Génica/genética , Inflamación/metabolismo , Masculino , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados
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