A shared transcriptional network in the nucleus accumbens supports resilience to chronic stress across sex.
Gyles, T. M.; Holt, L. M.; Parise, L. F.; Fisher, R.; Godino, A.; Browne, C. J.; Kipp, B.; Minier-Toribio, A.; Markovic, T.; Daly, T.; Durand, R.; Li, L.; Ramakrishnan, A.; Estill, M.; Rivera, M.; Yim, Y. Y.; Carona-Acosta, A.; Sial, O.; Nwakama, C.; Bolanos-Guzman, C.; Shen, L.; Zhang, B.; Russo, S.; Parise, E.; Nestler, E. J.
Show 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.
Matching journals
The top 3 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Early life stress alters transcriptomic patterning across reward circuitry in male and female mice 97%
- Stress-induced epigenetic regulation of transcription in neocortical excitatory neurons drives depression-like behavior 97%
- SWI/SNF chromatin remodeler complex within the reward pathway is required for behavioral adaptations to stress 95%
Similar papers in this journal
- Transcriptome signatures of the medial prefrontal cortex underlying GABAergic control of resilience to chronic stress exposure 97%
- Sex-specific GABAergic microcircuits that switch vulnerability into resilience to stress and reverse the effects of chronic stress exposure 96%
- ACh signaling modulates activity of the GABAergic signaling network in the basolateral amygdala and behavior in stress-relevant paradigms. 94%
Similar papers in this journal
- Identification of a stress-sensitive endogenous opioid-containing neuronal population in the paranigral ventral tegmental area. 96%
- Prefrontal allopregnanolone mediates the adverse effects of acute stress in a mouse model of tic pathophysiology 94%
- Transcriptomic signatures of sex-specific nicotine sensitization and imprinting of self-administration in rats inform GWAS findings on human addiction phenotypes 94%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.