A shared transcriptional network in the nucleus accumbens supports resilience to chronic stress across sex.
Trevonn M. GylesiD, Leanne Melissa HoltiD, Lyonna F. PariseiD, Rachel L. Fisher-Foye, Arthur GodinoiD, Caleb J. BrowneiD, Brian T. Kipp, Angelica M. Minier-ToribioiD, Tamara MarkoviciD, Teagan Daly, Romain Durand-de CuttoliiD, Long LiiD, Aarthi RamakrishnaniD, Molly S. EstilliD, Matthew T. RiveraiD, Yun Young YimiD, Astrid Carona-Acosta, Omar K. SialiD, Chinonso A. NwakamaiD, Carlos A. Bolaños‐GuzmániD, Li SheniD, Bin Zhang, Scott J. RussoiD, Eric M. PariseiD, Eric J. NestleriD
Abstract
Although chronic stress increases the risk for depression, only a subset of exposed individuals develop psychiatric illness. The biological mechanisms that protect against depression remain incompletely understood, particularly at the molecular level. Here, we identify a transcriptional network in the nucleus accumbens (NAc), a central brain reward region, that supports stress resilience in both sexes and demonstrate the causal contribution of key hub genes. Using chronic social defeat stress, RNA-seq, and co-expression network analysis, we find sex-specific but overlapping gene modules linked to resilience, anchored by shared hub genes embedded within a common network architecture. Overexpression of these hub genes in stress-naive mice confers stress protection and induces a transcriptional state that is discrete from both susceptible and resilient profiles. These findings position resilience as a structured and targetable molecular phenotype and provide a basis for investigating sex-informed mechanisms of stress adaptation.
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