Nash Family Department of Neuroscience, Center for Glial Biology, Ronald M. Loeb Center for Alzheimer's Disease, Precision Immunology Institute, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Nash Family Department of Neuroscience, Center for Glial Biology, Ronald M. Loeb Center for Alzheimer's Disease, Precision Immunology Institute, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Curr Opin Immunol. 2020 Feb;62:123-130. doi: 10.1016/j.coi.2020.01.003. Epub 2020 Feb 10.
External organic or inorganic objects (foreign bodies) that are inadvertently or purposefully placed in the human or animal tissues can trigger local tissue responses that aim at the elimination and/or segregation of foreign bodies from the tissue. The foreign body response (FBR) may have major implications for neurodegeneration associated with the formation of aberrant protein-based aggregates or plaques. The distinct physical features of the plaques, including high rigidity and varying surface properties, may trigger microglial mechanosensing of the plaque as a foreign body. The microglial FBR may have a dual function by promoting and/or suppressing the plaque driven neurodegeneration. Microglial contact with the plaque may trigger inflammatory activation of microglia and support microglia-driven neuronal damage. Conversely, persistent microglial activation may trigger the formation of a microglia-supported cell barrier that segregates and compacts the plaques thus preventing further plaque-induced damage to healthy neurons.
无意中或有意放置在人体或动物组织中的外部有机或无机物体(异物)会引发局部组织反应,旨在将异物从组织中清除和/或隔离。异物反应(FBR)可能与形成异常蛋白为基础的聚集物或斑块相关的神经退行性变有重大关系。斑块的独特物理特征,包括高刚性和不同的表面性质,可能会触发小胶质细胞对斑块作为异物的机械感应。小胶质细胞的 FBR 可能具有双重功能,既能促进又能抑制斑块驱动的神经退行性变。小胶质细胞与斑块的接触可能会引发小胶质细胞的炎症激活,并支持小胶质细胞驱动的神经元损伤。相反,持续的小胶质细胞激活可能会触发小胶质细胞支持的细胞屏障的形成,将斑块隔离和压缩,从而防止进一步的斑块诱导的健康神经元损伤。