Department of Chemistry & Biochemistry, University of Missouri-St. Louis, St. Louis, Missouri, USA.
Axe Neurosciences, Centre de Recherche du CHU de Québec-Université Laval, Québec, Quebec, Canada.
J Neurochem. 2019 Jun;149(5):562-581. doi: 10.1111/jnc.14674. Epub 2019 Mar 27.
This review discusses the profound connection between microglia, neuroinflammation, and Alzheimer's disease (AD). Theories have been postulated, tested, and modified over several decades. The findings have further bolstered the belief that microglia-mediated inflammation is both a product and contributor to AD pathology and progression. Distinct microglia phenotypes and their function, microglial recognition and response to protein aggregates in AD, and the overall role of microglia in AD are areas that have received considerable research attention and yielded significant results. The following article provides a historical perspective of microglia, a detailed discussion of multiple microglia phenotypes including dark microglia, and a review of a number of areas where microglia intersect with AD and other pathological neurological processes. The overall breadth of important discoveries achieved in these areas significantly strengthens the hypothesis that neuroinflammation plays a key role in AD. Future determination of the exact mechanisms by which microglia respond to, and attempt to mitigate, protein aggregation in AD may lead to new therapeutic strategies.
这篇综述讨论了小胶质细胞、神经炎症与阿尔茨海默病(AD)之间的深刻关联。几十年来,相关理论不断被提出、检验和修正。这些发现进一步证实了小胶质细胞介导的炎症既是 AD 病理和进展的产物,也是其促成因素。小胶质细胞表型及其功能的差异、小胶质细胞对 AD 中蛋白聚集的识别和反应,以及小胶质细胞在 AD 中的整体作用,是受到广泛关注并取得重要成果的领域。本文提供了小胶质细胞的历史视角,详细讨论了多种小胶质细胞表型,包括暗小胶质细胞,并回顾了小胶质细胞与 AD 和其他病理性神经过程交叉的多个领域。这些领域取得的重要发现范围广泛,有力地支持了神经炎症在 AD 中发挥关键作用的假说。未来确定小胶质细胞对 AD 中蛋白聚集的反应及试图减轻其影响的确切机制,可能会带来新的治疗策略。