| Literature DB >> 27791080 |
Hirobumi Tada1, Tomoyuki Miyazaki1, Kiwamu Takemoto1,2, Kenkichi Takase3, Susumu Jitsuki1, Waki Nakajima1, Mayu Koide1, Naoko Yamamoto1, Kasane Komiya1, Kumiko Suyama1, Akane Sano1, Akiko Taguchi4, Takuya Takahashi5.
Abstract
Social separation early in life can lead to the development of impaired interpersonal relationships and profound social disorders. However, the underlying cellular and molecular mechanisms involved are largely unknown. Here, we found that isolation of neonatal rats induced glucocorticoid-dependent social dominance over nonisolated control rats in juveniles from the same litter. Furthermore, neonatal isolation inactivated the actin-depolymerizing factor (ADF)/cofilin in the juvenile medial prefrontal cortex (mPFC). Isolation-induced inactivation of ADF/cofilin increased stable actin fractions at dendritic spines in the juvenile mPFC, decreasing glutamate synaptic AMPA receptors. Expression of constitutively active ADF/cofilin in the mPFC rescued the effect of isolation on social dominance. Thus, neonatal isolation affects spines in the mPFC by reducing actin dynamics, leading to altered social behavior later in life.Entities:
Keywords: AMPA receptor trafficking; actin dynamics; medial prefrontal cortex; social dominance; social isolation stress
Year: 2016 PMID: 27791080 PMCID: PMC5111648 DOI: 10.1073/pnas.1606351113
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205