| Literature DB >> 31482401 |
Luisa Lo Iacono1,2, Donald Ielpo1,3, Alessandra Accoto1, Matteo Di Segni1,2, Lucy Babicola4, Sebastian Luca D'Addario1,3, Fabio Ferlazzo1, Tiziana Pascucci1,2, Rossella Ventura5,6, Diego Andolina7,8.
Abstract
Chronic stress exposure is known to increase vulnerability to the expression of psychiatric disorders, such as depression. Clinical and preclinical evidences support the involvement of the microRNA-34 family in stress-related psychiatric conditions and in the regulation of stress responses. However, the mechanism and the multiple targets by which the microRNA-34 family can affect the stress response and stress-related behavioral alteration are not fully known. Here, with the aid of constitutive and conditional genetic strategy, we examined the role of microRNA-34 family in the expression of depression-like phenotype in mice induced by chronic stress exposure, and we identified their "in vivo" targets during the stressful challenge. We found that microRNA-34a, under chronic stress, is significantly up-regulated in the mouse raphe nuclei, where its recruitment is necessary to induce depression-like behavioral alterations and impact the function of the serotonergic system. Moreover, by next-generation RNA-seq of Ago-2-bound mRNAs, we identified genes that are targeted by microRNA-34a in response to chronic stress and that are likely to mediate its effects.Entities:
Keywords: Ago2, RISC-Seq; Chronic stress; Depression-like behavior; MicroRNA-34; Raphe nuclei; Serotonin
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Year: 2019 PMID: 31482401 DOI: 10.1007/s12035-019-01750-2
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.590