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  Amygdalar MicroRNA-15a Is Essential for Coping with Chronic Stress.

Volk, N., Pape, J. C., Engel, M., Zannas, A. S., Cattane, N., Cattaneo, A., et al. (2016). Amygdalar MicroRNA-15a Is Essential for Coping with Chronic Stress. Cell reports, 17(7), 1882-1891. doi:10.1016/j.celrep.2016.10.038.

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 Urheber:
Volk, Naama1, 2, Autor           
Pape, Julius C.1, 3, Autor           
Engel, Mareen2, Autor           
Zannas, Anthony S.3, Autor           
Cattane, Nadia1, Autor
Cattaneo, Annamaria1, Autor
Binder, Elisabeth B.1, 3, Autor           
Chen, Alon1, 2, Autor           
Affiliations:
1external, ou_persistent22              
2Dept. Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Max Planck Society, ou_2035294              
3Dept. Translational Research in Psychiatry, Max Planck Institute of Psychiatry, Max Planck Society, ou_2035295              

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 Zusammenfassung: MicroRNAs are important regulators of gene expression and associated with stress-related psychiatric disorders. Here, we report that exposing mice tochronic stress led to a specific increase in microRNA-15a levels in the amygdala-Ago2 complex and a concomitant reduction in the levels of its predicted target, FKBP51, which is implicated in stress-related psychiatric disorders. Reciprocally, mice expressing reduced levels of amygdalar microRNA-15a following exposure to chronic stress exhibited increased anxiety-like behaviors. In humans, pharmacological activation of the glucocorticoid receptor, as well as exposure to childhood trauma, was associated with increased microRNA-15a levels in peripheral blood. Taken together, our results support an important role for microRNA-15ain stress adaptation and the pathogenesis of stress-related psychopathologies.

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Sprache(n): eng - English
 Datum: 2016
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: ISI: 27829158
DOI: 10.1016/j.celrep.2016.10.038
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Projektname : Gxe Molmech, Grant ID: 281338; FP7, Grant ID 260463
Grant ID : -
Förderprogramm : Funding Programme 7 (FP7)
Förderorganisation : European Commission (EC)

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Titel: Cell reports
Genre der Quelle: Zeitschrift
 Urheber:
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Ort, Verlag, Ausgabe: Cambridge, MA 02139 USA : Cell Press
Seiten: - Band / Heft: 17 (7) Artikelnummer: - Start- / Endseite: 1882 - 1891 Identifikator: -