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肠道功能的神经免疫调节

Neuroimmune Modulation of Gut Function.

作者信息

Shea-Donohue Terez, Urban Joseph F

机构信息

Department of Radiation Oncology, University of Maryland School of Medicine, DTRS, MSTF Rm 700C, 10 Pine Street, Baltimore, MD, 21201, USA.

Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, 21201, USA.

出版信息

Handb Exp Pharmacol. 2017;239:247-267. doi: 10.1007/164_2016_109.

Abstract

Neuroimmune communications are facilitated by the production of neurotransmitters by immune cells and the generation of immune mediators by immune cells, which form a functional entity called the "neuroimmune synapse." There are several mechanisms that further facilitate neuroimmune interactions including the anatomic proximity between immune cells and nerves, the expression of receptors for neurotransmitters on immune cells and for immune mediators on nerves, and the receptor-mediated activation of intracellular signaling pathways that modulate nerve and immune phenotype and function. The bidirectional communication between nerves and immune cells is implicated in allostasis, a process that describes the continuous adaptation to an ever-changing environment. Neuroimmune interactions are amplified during inflammation by the influx of activated immune cells that significantly alter the microenvironment. In this context, the types of neurotransmitters released by activated neurons or immune cells can exert pro- or anti-inflammatory effects. Dysregulation of the enteric nervous system control of gastrointestinal functions, such as epithelial permeability and secretion as well as smooth muscle contractility, also contribute to the chronicity of inflammation. Persistent active inflammation in the gut leads to neuroimmune plasticity, which is a structural and functional remodeling in both the neural and immune systems. The importance of neuroimmune interactions has made them an emerging target in the development of novel therapies for GI pathologies.

摘要

神经免疫通讯通过免疫细胞产生神经递质以及免疫细胞产生免疫介质来促进,这些共同形成了一个被称为“神经免疫突触”的功能实体。还有几种机制进一步促进神经免疫相互作用,包括免疫细胞与神经之间的解剖学邻近性、免疫细胞上神经递质受体以及神经上免疫介质受体的表达,以及受体介导的细胞内信号通路激活,这些信号通路可调节神经和免疫表型及功能。神经与免疫细胞之间的双向通讯参与了适应性稳态,这是一个描述对不断变化的环境持续适应的过程。在炎症期间,活化免疫细胞的涌入会显著改变微环境,从而放大神经免疫相互作用。在这种情况下,活化神经元或免疫细胞释放的神经递质类型可发挥促炎或抗炎作用。肠道神经系统对胃肠道功能(如上皮通透性、分泌以及平滑肌收缩性)控制的失调,也会导致炎症的慢性化。肠道中持续的活动性炎症会导致神经免疫可塑性,这是神经和免疫系统的结构和功能重塑。神经免疫相互作用的重要性使其成为胃肠道疾病新型疗法开发中一个新兴的靶点。

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