D'Andrea Michael R, Cole Gregory M, Ard March D
Drug Discovery, Johnson & Johnson Pharmaceutical Research and Development, D404, Spring House, PA 19477, USA.
Neurobiol Aging. 2004 May-Jun;25(5):675-83. doi: 10.1016/j.neurobiolaging.2003.12.026.
Alzheimer disease (AD) involves glial inflammation associated with amyloid plaques. The role of the microglial cells in the AD brain is controversial, as it remains unclear if the microglia form the amyloid fibrils of plaques or react to them in a macrophage-phagocytic role. Also, it is not known why microglia are preferentially associated with some amyloid plaque types. This review will provide substantial evidence to support the phagocytic role of microglia in the brain as well as explain why microglia are generally associated with specific plaque types that may be explained through their unique mechanisms of formation. In summary, the data presented suggests that plaque associated microglial activation is typically subsequent to specific amyloid plaque formations in the AD brain.
阿尔茨海默病(AD)涉及与淀粉样斑块相关的神经胶质炎症。小胶质细胞在AD大脑中的作用存在争议,因为目前尚不清楚小胶质细胞是形成斑块的淀粉样纤维还是以巨噬细胞吞噬的作用对其做出反应。此外,也不清楚为什么小胶质细胞优先与某些类型的淀粉样斑块相关联。本综述将提供大量证据来支持小胶质细胞在大脑中的吞噬作用,并解释为什么小胶质细胞通常与特定的斑块类型相关,这可能通过其独特的形成机制来解释。总之,所呈现的数据表明,在AD大脑中,与斑块相关的小胶质细胞激活通常发生在特定淀粉样斑块形成之后。