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Orphan receptor GPR158 controls stress-induced depression.
Sutton, Laurie P; Orlandi, Cesare; Song, Chenghui; Oh, Won Chan; Muntean, Brian S; Xie, Keqiang; Filippini, Alice; Xie, Xiangyang; Satterfield, Rachel; Yaeger, Jazmine D W; Renner, Kenneth J; Young, Samuel M; Xu, Baoji; Kwon, Hyungbae; Martemyanov, Kirill A.
Afiliación
  • Sutton LP; Department of Neuroscience, The Scripps Research Institute, Jupiter, United States.
  • Orlandi C; Department of Neuroscience, The Scripps Research Institute, Jupiter, United States.
  • Song C; Department of Neuroscience, The Scripps Research Institute, Jupiter, United States.
  • Oh WC; Max Planck Florida Institute for Neuroscience, Jupiter, United States.
  • Muntean BS; Department of Neuroscience, The Scripps Research Institute, Jupiter, United States.
  • Xie K; Department of Neuroscience, The Scripps Research Institute, Jupiter, United States.
  • Filippini A; Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
  • Xie X; Department of Neuroscience, The Scripps Research Institute, Jupiter, United States.
  • Satterfield R; Max Planck Florida Institute for Neuroscience, Jupiter, United States.
  • Yaeger JDW; Center for Brain and Behavior Research, University of South Dakota, Vermillion, United States.
  • Renner KJ; Department of Biology, University of South Dakota, Vermillion, United States.
  • Young SM; Center for Brain and Behavior Research, University of South Dakota, Vermillion, United States.
  • Xu B; Department of Biology, University of South Dakota, Vermillion, United States.
  • Kwon H; Max Planck Florida Institute for Neuroscience, Jupiter, United States.
  • Martemyanov KA; Department of Anatomy and Cell Biology, University of Iowa, Iowa, United States.
Elife ; 72018 02 08.
Article en En | MEDLINE | ID: mdl-29419376
Stress can be a motivational force for decisive action and adapting to novel environment; whereas, exposure to chronic stress contributes to the development of depression and anxiety. However, the molecular mechanisms underlying stress-responsive behaviors are not fully understood. Here, we identified the orphan receptor GPR158 as a novel regulator operating in the prefrontal cortex (PFC) that links chronic stress to depression. GPR158 is highly upregulated in the PFC of human subjects with major depressive disorder. Exposure of mice to chronic stress also increased GPR158 protein levels in the PFC in a glucocorticoid-dependent manner. Viral overexpression of GPR158 in the PFC induced depressive-like behaviors. In contrast GPR158 ablation, led to a prominent antidepressant-like phenotype and stress resiliency. We found that GPR158 exerts its effects via modulating synaptic strength altering AMPA receptor activity. Taken together, our findings identify a new player in mood regulation and introduce a pharmacological target for managing depression.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 Problema de salud: 1_doencas_nao_transmissiveis Asunto principal: Estrés Psicológico / Regulación de la Expresión Génica / Corteza Prefrontal / Receptores Acoplados a Proteínas G / Depresión Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Elife Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 Problema de salud: 1_doencas_nao_transmissiveis Asunto principal: Estrés Psicológico / Regulación de la Expresión Génica / Corteza Prefrontal / Receptores Acoplados a Proteínas G / Depresión Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Elife Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos
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