在全身炎症和感染刺激下,血液如何与脑实质和下丘脑室旁核对话。

S Rivest, S Lacroix, L Vallières, S Nadeau, J Zhang, N Laflamme
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引用次数: 158

摘要

在系统性免疫挑战中,血脑屏障(BBB)细胞内循环促炎分子影响的分子机制有了令人兴奋的新进展。当这些分子存在于循环中时,具有触发一系列级联事件的能力,导致在中枢神经系统(CNS)血管相关细胞中分裂原活化蛋白(MAP)激酶/核因子κ B (nf - κ B)或janus激酶(JAK)/信号转导和转录激活因子(STAT)转导途径。脑血管表现出不同促炎配体受体的组成和诱导表达,这些配体具有刺激这些信号分子的能力。根据所涉及的挑战和细胞因子,血脑屏障细胞中征求的转导信号可能以一种非常特定的方式定向神经元活动,以激活转录和产生可溶性因子,如前列腺素(pg)。有趣的是,细胞因子和全身性局部炎症以一种非选择性的方式刺激血脑屏障细胞(即,在大血管和小毛细血管中)。这种非选择性提出了几个关于由不同的炎症和细胞因子实验模型诱导的局部神经元激活的问题。神经元反应的选择性可能是可溶性介质的非实质合成和这些配体的特异性受体在不同脑核实质成分中的表达之间精细相互作用的结果。本文将介绍这一概念的最新进展,以及发生在血脑屏障细胞中的机制,在全身免疫原性挑战中,血脑屏障细胞导致神经元回路参与恢复机体的稳态。发热的诱导、下丘脑-垂体-肾上腺(HPA)轴和其他自主神经功能是哺乳动物机体在外来物质存在时保护所必需的生理结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
How the blood talks to the brain parenchyma and the paraventricular nucleus of the hypothalamus during systemic inflammatory and infectious stimuli.

There are exciting new developments regarding the molecular mechanisms involved in the influence of circulating proinflammatory molecules within cells of the blood-brain barrier (BBB) during systemic immune challenges. These molecules, when present in the circulation, have the ability to trigger a series of events in cascade, leading to either the mitogen-activated protein (MAP) kinases/nuclear factor kappa B (NF-kappaB) or the janus kinase (JAK)/signal transducer and activator of transcription (STAT) transduction pathways in vascular-associated cells of the central nervous system (CNS). The brain blood vessels exhibit both constitutive and induced expression of receptors for different proinflammatory ligands that have the ability to stimulate these signaling molecules. Depending on the challenges and the cytokines involved, the transduction signal(s) solicited in cells of the BBB may orient the neuronal activity in a very specific manner in activating the transcription and production of soluble factors, such as prostaglandins (PGs). It is interesting to note that cytokines as well as systemic localized inflammation stimulate the cells of the BBB in a nonselective manner (i.e., within both large blood vessels and small capillaries across the brain). This nonselectivity raises several questions with regard to the localized neuronal activation induced by different experimental models of inflammation and cytokines. It is possible that the selectivity of the neuronal response is a consequence of the fine interaction between nonparenchymal synthesis of soluble mediators and expression of specific receptors for these ligands within parenchymal elements of different brain nuclei. This review will present the recent developments on this concept and the mechanisms that take place in cells of the BBB, which lead to the neuronal circuits involved in restoring the body's homeostasis during systemic immunogenic challenges. The induction of fever, the hypothalamic-pituitary adrenal (HPA) axis, and other autonomic functions are among the physiological outcomes necessary for the protection of the mammalian organism in the presence of foreign material.

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