دورية أكاديمية

p53 in AgRP neurons is required for protection against diet-induced obesity via JNK1.

التفاصيل البيبلوغرافية
العنوان: p53 in AgRP neurons is required for protection against diet-induced obesity via JNK1.
المؤلفون: Quiñones, M., Al-Massadi, O., Folgueira, C., Bremser, S., Gallego, R., Torres-Leal, L., Haddad-Tóvolli, R., García-Cáceres, C., Hernandez-Bautista, R., Lam, B.Y.H., Beiroa, D., Sanchez-Rebordelo, E., Senra, A., Malagon, J.A., Valerio, P., Fondevila, M.F., Fernø, J., Malagon, M.M., Contreras, R., Pfluger, P.T., Brüning, J.C., Yeo, G., Tschöp, M.H., Diéguez, C., López, M., Claret, M., Kloppenburg, P., Sabio, G., Nogueiras, R.
المصدر: Nat. Commun. 9:3432 (2018)
بيانات النشر: Nature Publishing Group
سنة النشر: 2018
المجموعة: PuSH - Publikationsserver des Helmholtz Zentrums München
الوصف: p53 is a well-known tumor suppressor that has emerged as an important player in energy balance. However, its metabolic role in the hypothalamus remains unknown. Herein, we show that mice lacking p53 in agouti-related peptide (AgRP), but not proopiomelanocortin (POMC) or steroidogenic factor-1 (SF1) neurons, are more prone to develop diet-induced obesity and show reduced brown adipose tissue (BAT) thermogenic activity. AgRP-specific ablation of p53 resulted in increased hypothalamic c-Jun N-terminal kinase (JNK) activity before the mice developed obesity, and central inhibition of JNK reversed the obese phenotype of these mice. The overexpression of p53 in the ARC or specifically in AgRP neurons of obese mice decreased body weight and stimulated BAT thermogenesis, resulting in body weight loss. Finally, p53 in AgRP neurons regulates the ghrelin-induced food intake and body weight. Overall, our findings provide evidence that p53 in AgRP neurons is required for normal adaptations against diet-induced obesity.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
تدمد: 2041-1723
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30143607; info:eu-repo/semantics/altIdentifier/wos/WOS:000442594800034; info:eu-repo/semantics/altIdentifier/isbn/2041-1723; info:eu-repo/semantics; https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=54186Test; urn:isbn:2041-1723; urn:issn:2041-1723
DOI: 10.1038/s41467-018-05711-6
الإتاحة: https://doi.org/10.1038/s41467-018-05711-6Test
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=54186Test
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.9C576B1E
قاعدة البيانات: BASE
الوصف
تدمد:20411723
DOI:10.1038/s41467-018-05711-6