Biological Psychiatry Unit, IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Brescia, Italy.
Behavioral Pharmacology Laboratory, Maj Institute of Pharmacology, Polish Academy of Sciences, Kraków, Poland.
Brain Behav Immun. 2024 Oct;121:340-350. doi: 10.1016/j.bbi.2024.07.035. Epub 2024 Jul 27.
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.
压力是精神障碍发展的一个主要风险因素,包括抑郁症。然而,其影响并非在所有个体中都相同,因为只有一部分暴露于压力下的个体最终会出现负面的心理结果,而另一些个体则可以被认为是有弹性的。然而,导致脆弱或有弹性表型发展的生物学过程仍知之甚少。为了弥补这一不足,我们在这里使用了基于转录组和 miRNA 组学的方法,研究了对照组(CON)和慢性轻度应激(CMS)范式暴露的大鼠腹侧海马中的生物过程,然后根据蔗糖消耗测试将这些大鼠分为脆弱(VULN)或有弹性(RES)动物。与 CON 和 RES 动物组相比,VULN 大鼠的转录组分析显示炎症/免疫相关途径的激活,特别是涉及抗体和细胞因子产生的途径,以及参与蛋白质合成的途径的抑制。相反,RES 动物的转录组数据表明,几种涉及神经递质传递的途径被激活。然后,我们通过 miRComb R 包进行了 mRNA-miRNA 整合分析,发现最显著的 mRNA-miRNA 对参与促进 VULN 动物的炎症状态,并在 RES 大鼠中降低其水平。此外,在 VULN 动物中,mRNA-miRNA 联合分析揭示了嗅觉感觉系统的调节,这是一个关键的生物学过程,已经发现其与抑郁症等与压力相关的疾病的发病机制有关。总的来说,我们基于 mRNA-miRNA 整合的方法确定了不同的生物学过程,这些过程与 CMS 暴露的负面效应下脆弱或有弹性表型的发展相关,这可能为预防或治疗提供新的靶点。