Early life stress confers lifelong stress susceptibility in mice via ventral tegmental area OTX2
Author(s) -
Catherine J. Peña,
Hope Kronman,
Deena M. Walker,
Hannah M. Cates,
Rosemary C. Bagot,
Immanuel Purushothaman,
Orna Issler,
YongHwee Eddie Loh,
Tin Leong,
Drew D. Kiraly,
Emma Goodman,
Rachael L. Neve,
Li Shen,
Eric J. Nestler
Publication year - 2017
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aan4491
Subject(s) - ventral tegmental area , stress (linguistics) , biology , neuroscience , psychology , dopamine , dopaminergic , linguistics , philosophy
Early life stress increases risk for depression. Here we establish a "two-hit" stress model in mice wherein stress at a specific postnatal period increases susceptibility to adult social defeat stress and causes long-lasting transcriptional alterations that prime the ventral tegmental area (VTA)-a brain reward region-to be in a depression-like state. We identify a role for the developmental transcription factor orthodenticle homeobox 2 ( Otx2 ) as an upstream mediator of these enduring effects. Transient juvenile-but not adult-knockdown of Otx2 in VTA mimics early life stress by increasing stress susceptibility, whereas its overexpression reverses the effects of early life stress. This work establishes a mechanism by which early life stress encodes lifelong susceptibility to stress via long-lasting transcriptional programming in VTA mediated by Otx2 .
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