Molecular mechanisms underlying stress vulnerability and resilience in the chronic mild stress model: New insights from mRNA and miRNAs data combining

• Published in: Brain, behavior, and immunity Vol. 121; pp. 340 - 350
• Main Authors: Cattane, Nadia, Mazzelli, Monica, Begni, Veronica, Mombelli, Elisa, Papp, Mariusz, Maj, Carlo, Riva, Marco Andrea, Cattaneo, Annamaria
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 01.10.2024
• Subjects: Chronic mild stress; Gene expression; microRNAs; Resilience; Ventral hippocampus; Vulnerability; microRNAs; Ventral hippocampus; Chronic mild stress; Vulnerability; Gene expression; Resilience
• ISSN: 0889-1591; 1090-2139; 1090-2139
• DOI: 10.1016/j.bbi.2024.07.035

•Transcriptomic analyses revealed the activation of inflammatory-related pathways in VULN rats.•Transcriptomic analyses revealed the inhibition of pathways involved in protein synthesis in VULN rats.•Transcriptomic analyses suggested the activation of pathways involved in neurotransmission in RES rats.•Most significant mRNA-miRNA pairs were involved in inflammation and in the olfactory sensory system in VULN rats. Stress is a major risk factor for the development of psychiatric disorders, including depression. However, its effects are not the same in all the subjects as only a portion of individuals exposed to stress will eventually develop negative mental outcomes, while others can be considered resilient. However, the biological processes underlying the development of a vulnerable or resilient phenotype are still poor understood. In order to cover this, we here used both transcriptomic and miRNomic based approaches in the ventral hippocampus of control (CON) and rats exposed to the chronic mild stress (CMS) paradigm, which were then divided into vulnerable (VULN) or resilient (RES) animals according to the sucrose consumption test. Transcriptomic analyses in VULN rats, compared to both the group of CON and RES animals, revealed the activation of inflammatory/immune-related pathways, specifically involved in antibodies and cytokine production, and the inhibition of pathways involved in protein synthesis. Conversely, transcriptomic data in RES animals suggested the activation of several pathways involved in neurotransmission. We then performed a mRNA-miRNA integration analysis by using miRComb R package, and we found that the most significant mRNA-miRNA pairs were involved in promoting the inflammatory status in VULN animals and, vice versa, by decreasing it in RES rats. Moreover, in VULN animals, the mRNA-miRNA combining analyses revealed the modulation of the olfactory sensory system, a key biological process that has been already found involved in the etiology of stress related disorders such as depression. Overall, our mRNA-miRNA integration-based approach identified distinct biological processes that are relevant for the development of a vulnerable or resilient phenotype in response to the negative effects of CMS exposure, which could allow the identification of novel targets for prevention or treatment.