Maternal n-3 enriched diet reprograms the offspring neurovascular transcriptome and blunts inflammation induced by endotoxin in the neonate.

IF 9.3 1区 医学 Q1 IMMUNOLOGY
Tetyana Chumak, Amandine Jullienne, C Joakim Ek, Maryam Ardalan, Pernilla Svedin, Ryan Quan, Arjang Salehi, Sirus Salari, Andre Obenaus, Zinaida S Vexler, Carina Mallard
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引用次数: 0

Abstract

Infection during the perinatal period can adversely affect brain development, predispose infants to ischemic stroke and have lifelong consequences. We previously demonstrated that diet enriched in n-3 polyunsaturated fatty acids (n-3 PUFA) transforms brain lipid composition in the offspring and protects the neonatal brain from stroke, in part by blunting injurious immune responses. Critical to the interface between the brain and systemic circulation is the vasculature, endothelial cells in particular, that support brain homeostasis and provide a barrier to systemic infection. Here, we examined whether maternal PUFA-enriched diets exert reprograming of endothelial cell signalling in postnatal day 9 mice after modeling aspects of infection using LPS. Transcriptome analysis was performed on microvessels isolated from brains of pups from dams maintained on 3 different maternal diets from gestation day 1: standard, n-3 enriched or n-6 enriched diets. Depending on the diet, in endothelial cells LPS produced distinct regulation of pathways related to immune response, cell cycle, extracellular matrix, and angiogenesis. N-3 PUFA diet enabled higher immune reactivity in brain vasculature, while preventing imbalance of cell cycle regulation and extracellular matrix cascades that accompanied inflammatory response in standard diet. Cytokine analysis revealed a blunted LPS response in blood and brain of offspring from dams on n-3 enriched diet. Analysis of cerebral vasculature in offspring in vivo revealed no differences in vessel density. However, vessel complexity was decreased in response to LPS at 72 h in standard and n-6 diets. Thus, LPS modulates specific transcriptomic changes in brain vessels of offspring rather than major structural vessel characteristics during early life. N-3 PUFA-enriched maternal diet in part prevents an imbalance in homeostatic processes, alters inflammation and ultimately mitigates changes to the complexity of surface vessel networks that result from infection. Importantly, maternal diet may presage offspring neurovascular outcomes later in life.

母体富含 n-3 的饮食可重编后代神经血管转录组,并减缓新生儿由内毒素诱发的炎症。
围产期感染会对大脑发育产生不利影响,使婴儿易患缺血性中风,并造成终生后果。我们以前曾证实,富含 n-3 多不饱和脂肪酸(n-3 PUFA)的饮食能改变后代的脑脂质组成,并保护新生儿大脑免受中风的影响,部分原因是它能抑制损伤性免疫反应。血管尤其是内皮细胞对大脑和全身循环之间的界面至关重要,它们支持大脑的平衡并为全身感染提供屏障。在此,我们研究了母体富含 PUFA 的膳食是否会在使用 LPS 模拟感染后对出生后第 9 天小鼠的内皮细胞信号进行重编程。研究人员对从妊娠第 1 天起使用 3 种不同母体膳食(标准膳食、富含 n-3 脂肪酸膳食或富含 n-6 脂肪酸膳食)的母鼠所产幼鼠大脑中分离出的微血管进行了转录组分析。根据饮食的不同,LPS 对内皮细胞中与免疫反应、细胞周期、细胞外基质和血管生成有关的通路产生了不同的调节作用。N-3 PUFA饮食可提高脑血管的免疫反应性,同时防止标准饮食中伴随炎症反应的细胞周期调节和细胞外基质级联失衡。细胞因子分析表明,食用富含 n-3 脂肪酸膳食的母鼠后代血液和大脑中的 LPS 反应减弱。对后代体内脑血管的分析表明,血管密度没有差异。然而,在标准膳食和 n-6 膳食中,72 h 后代的血管复杂性对 LPS 的反应有所降低。因此,LPS 在生命早期会调节后代脑血管的特定转录组变化,而不是主要的血管结构特征。富含 N-3 PUFA 的母体膳食在一定程度上防止了体内平衡过程的失衡,改变了炎症,并最终减轻了感染导致的表面血管网络复杂性的变化。重要的是,母体饮食可能预示着后代神经血管日后的结果。
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来源期刊
Journal of Neuroinflammation
Journal of Neuroinflammation 医学-神经科学
CiteScore
15.90
自引率
3.20%
发文量
276
审稿时长
1 months
期刊介绍: The Journal of Neuroinflammation is a peer-reviewed, open access publication that emphasizes the interaction between the immune system, particularly the innate immune system, and the nervous system. It covers various aspects, including the involvement of CNS immune mediators like microglia and astrocytes, the cytokines and chemokines they produce, and the influence of peripheral neuro-immune interactions, T cells, monocytes, complement proteins, acute phase proteins, oxidative injury, and related molecular processes. Neuroinflammation is a rapidly expanding field that has significantly enhanced our knowledge of chronic neurological diseases. It attracts researchers from diverse disciplines such as pathology, biochemistry, molecular biology, genetics, clinical medicine, and epidemiology. Substantial contributions to this field have been made through studies involving populations, patients, postmortem tissues, animal models, and in vitro systems. The Journal of Neuroinflammation consolidates research that centers around common pathogenic processes. It serves as a platform for integrative reviews and commentaries in this field.
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