Laura Korobkova, Matthew E Thornton, Matthew A Collin, Elyse L Morin, Hadj Aoued, Soma Sannigrahi, Nabeel Bhinderwala, Kristie M Garza, Erin R Siebert, Hasse Walum, Ryan P Cabeen, Brendan H Grubbs, Mar M Sanchez, Brian G Dias
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Most investigations into biological processes that have been perturbed by ELA have profiled DNA methylation in whole blood and coalesced around perturbations of immunobiology being centrally insulted by ELA.</p><p><strong>Methods: </strong>To identify novel molecular signatures that are enduringly perturbed by childhood maltreatment, we isolated circulating extracellular vesicles (EVs) from plasma collected from adolescent rhesus macaques that had either experienced nurturing maternal care (CONT, n = 7, 4M 3F) or maltreatment in infancy (MALT, n = 6, 3M 3F). Next, we profiled the RNA found in these EVs.</p><p><strong>Results: </strong>RNA associated with genes related to translation, ATP synthesis, mitochondrial function and immune response were downregulated in circulating EVs collected from adolescent macaques that had experienced maltreatment during infancy, while those involved in ion transport, metabolism and cell differentiation were upregulated in these EVs. Additionally, a significant proportion of EV RNA aligned to the microbiome and maltreatment during infancy altered the diversity of microbiome-associated RNA signatures found in EVs.</p><p><strong>Conclusions: </strong>Our findings provide evidence that alterations in RNA associated with immune function, cellular energetics and the microbiome in circulating EVs may serve as enduring biomarkers of prior exposure to ELA. As a corollary, perturbations of these RNA profiles may offer novel molecular insight into how biology can remain altered long after the shadow of ELA has passed.</p>","PeriodicalId":8918,"journal":{"name":"Biological Psychiatry","volume":" ","pages":""},"PeriodicalIF":9.0000,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"RNA in plasma extracellular vesicles of adolescent rhesus macaques reveal immune, bioenergetic and microbial imprints of early life adversity - an exploratory analysis.\",\"authors\":\"Laura Korobkova, Matthew E Thornton, Matthew A Collin, Elyse L Morin, Hadj Aoued, Soma Sannigrahi, Nabeel Bhinderwala, Kristie M Garza, Erin R Siebert, Hasse Walum, Ryan P Cabeen, Brendan H Grubbs, Mar M Sanchez, Brian G Dias\",\"doi\":\"10.1016/j.biopsych.2025.08.020\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Exposure to early life adversity (ELA), including childhood maltreatment, is one of the most significant risk factors for the emergence of psychosomatic disorders in adolescence and adulthood. 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引用次数: 0
摘要
背景:暴露于早期生活逆境(ELA),包括童年虐待,是青春期和成年期出现心身疾病的最重要危险因素之一。大多数对受ELA干扰的生物过程的研究都描述了全血中的DNA甲基化,并结合了受ELA集中侮辱的免疫生物学的扰动。方法:为了鉴定受童年虐待持续干扰的新分子特征,我们从青春期恒河猴的血浆中分离出循环细胞外囊泡(ev),这些恒河猴要么经历过养育性的母亲照顾(CONT, n = 7, 4M 3F),要么经历过婴儿期的虐待(MALT, n = 6, 3M 3F)。接下来,我们分析了在这些ev中发现的RNA。结果:从幼年遭受虐待的青春期猕猴收集的循环ev中,与翻译、ATP合成、线粒体功能和免疫应答相关的基因RNA下调,而与离子转运、代谢和细胞分化相关的基因在这些ev中上调。此外,相当大比例的EV RNA与微生物组一致,婴儿期的虐待改变了EV中发现的微生物组相关RNA特征的多样性。结论:我们的研究结果提供了证据,证明循环ev中与免疫功能、细胞能量学和微生物组相关的RNA改变可能是先前暴露于ELA的持久生物标志物。作为推论,这些RNA谱的扰动可能提供新的分子见解,以了解在ELA阴影过去后,生物学是如何保持改变的。
RNA in plasma extracellular vesicles of adolescent rhesus macaques reveal immune, bioenergetic and microbial imprints of early life adversity - an exploratory analysis.
Background: Exposure to early life adversity (ELA), including childhood maltreatment, is one of the most significant risk factors for the emergence of psychosomatic disorders in adolescence and adulthood. Most investigations into biological processes that have been perturbed by ELA have profiled DNA methylation in whole blood and coalesced around perturbations of immunobiology being centrally insulted by ELA.
Methods: To identify novel molecular signatures that are enduringly perturbed by childhood maltreatment, we isolated circulating extracellular vesicles (EVs) from plasma collected from adolescent rhesus macaques that had either experienced nurturing maternal care (CONT, n = 7, 4M 3F) or maltreatment in infancy (MALT, n = 6, 3M 3F). Next, we profiled the RNA found in these EVs.
Results: RNA associated with genes related to translation, ATP synthesis, mitochondrial function and immune response were downregulated in circulating EVs collected from adolescent macaques that had experienced maltreatment during infancy, while those involved in ion transport, metabolism and cell differentiation were upregulated in these EVs. Additionally, a significant proportion of EV RNA aligned to the microbiome and maltreatment during infancy altered the diversity of microbiome-associated RNA signatures found in EVs.
Conclusions: Our findings provide evidence that alterations in RNA associated with immune function, cellular energetics and the microbiome in circulating EVs may serve as enduring biomarkers of prior exposure to ELA. As a corollary, perturbations of these RNA profiles may offer novel molecular insight into how biology can remain altered long after the shadow of ELA has passed.
期刊介绍:
Biological Psychiatry is an official journal of the Society of Biological Psychiatry and was established in 1969. It is the first journal in the Biological Psychiatry family, which also includes Biological Psychiatry: Cognitive Neuroscience and Neuroimaging and Biological Psychiatry: Global Open Science. The Society's main goal is to promote excellence in scientific research and education in the fields related to the nature, causes, mechanisms, and treatments of disorders pertaining to thought, emotion, and behavior. To fulfill this mission, Biological Psychiatry publishes peer-reviewed, rapid-publication articles that present new findings from original basic, translational, and clinical mechanistic research, ultimately advancing our understanding of psychiatric disorders and their treatment. The journal also encourages the submission of reviews and commentaries on current research and topics of interest.