| Literature DB >> 29339486 |
Mitra Heshmati1,2, Hossein Aleyasin1,2, Caroline Menard1,2, Daniel J Christoffel3, Meghan E Flanigan1,2, Madeline L Pfau1,2, Georgia E Hodes1,2, Ashley E Lepack1,2, Lucy K Bicks1,2, Aki Takahashi1,2,4, Ramesh Chandra5, Gustavo Turecki6, Mary Kay Lobo5, Ian Maze1,2, Sam A Golden7, Scott J Russo8,2.
Abstract
Behavioral coping strategies are critical for active resilience to stress and depression; here we describe a role for neuroligin-2 (NLGN-2) in the nucleus accumbens (NAc). Neuroligins (NLGN) are a family of neuronal postsynaptic cell adhesion proteins that are constituents of the excitatory and inhibitory synapse. Importantly, NLGN-3 and NLGN-4 mutations are strongly implicated as candidates underlying the development of neuropsychiatric disorders with social disturbances such as autism, but the role of NLGN-2 in neuropsychiatric disease states is unclear. Here we show a reduction in NLGN-2 gene expression in the NAc of patients with major depressive disorder. Chronic social defeat stress in mice also decreases NLGN-2 selectively in dopamine D1-positive cells, but not dopamine D2-positive cells, within the NAc of stress-susceptible mice. Functional NLGN-2 knockdown produces bidirectional, cell-type-specific effects: knockdown in dopamine D1-positive cells promotes subordination and stress susceptibility, whereas knockdown in dopamine D2-positive cells mediates active defensive behavior. These findings establish a behavioral role for NAc NLGN-2 in stress and depression; provide a basis for targeted, cell-type specific therapy; and highlight the role of active behavioral coping mechanisms in stress susceptibility.Entities:
Keywords: depression; dominance; medium spiny neuron; neuroligin-2; social defeat stress
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Year: 2018 PMID: 29339486 PMCID: PMC5798379 DOI: 10.1073/pnas.1719014115
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205