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PMID: 27773352 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

DCC Confers Susceptibility to Depression-like Behaviors in Humans and Mice and Is Regulated by miR-218.

Biological psychiatry ·Vol. 81 ·No. 4 ·2017-00-15 ·页码 306-315

Torres-Berrío A, Lopez JP, Bagot RC, Nouel D, Dal Bo G, Cuesta S, Zhu L, Manitt C, Eng C, Cooper HM, Storch KF, Turecki G, Nestler EJ, Flores C

Abstract

Variations in the expression of the Netrin-1 guidance cue receptor DCC (deleted in colorectal cancer) appear to confer resilience or susceptibility to psychopathologies involving prefrontal cortex (PFC) dysfunction. With the use of postmortem brain tissue, mouse models of defeat stress, and in vitro analysis, we assessed microRNA (miRNA) regulation of DCC and whether changes in DCC levels in the PFC lead to vulnerability to depression-like behaviors. We identified miR-218 as a posttranscriptional repressor of DCC and detected coexpression of DCC and miR-218 in pyramidal neurons of human and mouse PFC. We found that exaggerated expression of DCC and reduced levels of miR-218 in the PFC are consistent traits of mice susceptible to chronic stress and of major depressive disorder in humans. Remarkably, upregulation of Dcc in mouse PFC pyramidal neurons causes vulnerability to stress-induced social avoidance and anhedonia. These data are the first demonstration of microRNA regulation of DCC and suggest that, by regulating DCC, miR-218 may be a switch of susceptibility versus resilience to stress-related disorders.

Keywords
Chronic social defeat stress Guidance cue Major depressive disorder Neurodevelopment Resilience microRNA
MeSH 主题词
Animals Cell Line, Tumor DCC Receptor Depressive Disorder, Major/etiology,metabolism Humans Male Mice Mice, Inbred C57BL MicroRNAs/metabolism Prefrontal Cortex/metabolism Pyramidal Cells/metabolism RNA, Messenger/metabolism Receptors, Cell Surface/metabolism Social Behavior Stress, Psychological/complications Tumor Suppressor Proteins/metabolism
化学物质
DCC Receptor DCC protein, human MIRN218 microRNA, human MicroRNAs RNA, Messenger Receptors, Cell Surface Tumor Suppressor Proteins
作者与单位
共 14 位作者,点击展开单位 / ORCID
Torres-Berrío Angélica
Integrated Program in Neuroscience, Montréal, Québec, Canada; Douglas Mental Health University Institute; Montréal, Québec, Canada.
Lopez Juan Pablo
Department of Human Genetics; Montréal, Québec, Canada; McGill Group for Suicide Studies, Montréal, Québec, Canada.
Bagot Rosemary C
Departments of Psychology ; Montréal, Québec, Canada.
Nouel Dominique
Douglas Mental Health University Institute; Montréal, Québec, Canada.
Dal Bo Gregory
Douglas Mental Health University Institute; Montréal, Québec, Canada; Département de Toxicologie et risques chimiques, IRBA, Brétigny sur Orge, France.
Cuesta Santiago
Psychiatry, McGill University; Montréal, Québec, Canada; Douglas Mental Health University Institute; Montréal, Québec, Canada.
Zhu Lei
Douglas Mental Health University Institute; Montréal, Québec, Canada.
Manitt Colleen
Douglas Mental Health University Institute; Montréal, Québec, Canada.
Eng Conrad
Douglas Mental Health University Institute; Montréal, Québec, Canada.
Cooper Helen M
Queensland Brain Institute, The University of Queensland, Brisbane, Queensland, Australia.
Storch Kai-Florian
Psychiatry, McGill University; Montréal, Québec, Canada; Douglas Mental Health University Institute; Montréal, Québec, Canada.
Turecki Gustavo
Psychiatry, McGill University; Montréal, Québec, Canada; Douglas Mental Health University Institute; Montréal, Québec, Canada; McGill Group for Suicide Studies, Montréal, Québec, Canada.
Nestler Eric J
Fishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Flores Cecilia
Psychiatry, McGill University; Montréal, Québec, Canada; Douglas Mental Health University Institute; Montréal, Québec, Canada. Electronic address: cecilia.flores@mcgill.ca.
Article Info
Journal
Biological psychiatry
Abbr.
Biol Psychiatry
ISSN
1873-2402
Corresponding email
Published
2017-00-15
电子出版
2016-00-18
页码
306-315
Language
English
Country/Region
United States
NLM ID
0213264
基金资助
NIMH NIH HHS · P50 MH096890 · United States
NIDA NIH HHS · R01 DA037911 · United States
CIHR · MOP-74709 · Canada
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