Laboratorio de Neuroinmunología, Fundación Ciencia & Vida, Ñuñoa 7780272, Santiago, Chile.
Laboratorio de Neuroinmunología, Fundación Ciencia & Vida, Ñuñoa 7780272, Santiago, Chile; Facultad de Ciencias Biológicas, Universidad Andrés Bello, 8370146 Santiago, Chile.
J Neuroimmunol. 2014 Sep 15;274(1-2):1-13. doi: 10.1016/j.jneuroim.2014.07.012. Epub 2014 Jul 23.
Neuroinflammation constitutes a fundamental process involved in the progression of several neurodegenerative disorders, such as Parkinson's disease, Alzheimer's disease, amyotrophic lateral sclerosis and multiple sclerosis. Microglial cells play a central role in neuroinflammation, promoting neuroprotective or neurotoxic microenvironments, thus controlling neuronal fate. Acquisition of different microglial functions is regulated by intercellular interactions with neurons, astrocytes, the blood-brain barrier, and T-cells infiltrating the central nervous system. In this study, an overview of the regulation of microglial function mediated by different intercellular communications is summarised and discussed. Afterward, we focus in T-cell-mediated regulation of neuroinflammation involved in neurodegenerative disorders.
神经炎症是几种神经退行性疾病(如帕金森病、阿尔茨海默病、肌萎缩侧索硬化症和多发性硬化症)进展过程中的一个基本过程。小胶质细胞在神经炎症中起着核心作用,促进神经保护或神经毒性的微环境,从而控制神经元的命运。不同的小胶质细胞功能的获得受到与神经元、星形胶质细胞、血脑屏障以及浸润中枢神经系统的 T 细胞的细胞间相互作用的调节。在这项研究中,总结和讨论了不同细胞间通讯介导的小胶质细胞功能调节概述。之后,我们将重点关注 T 细胞介导的神经退行性疾病相关神经炎症的调节。