Schaible Philipp, Henschel Julia, Erny Daniel
Institute of Neuropathology, Medical Faculty, University of Freiburg, Breisacher Str. 64, 79106, Freiburg, Germany.
Faculty of Biology, University of Freiburg, Freiburg im Breisgau, Germany.
J Neuroinflammation. 2025 Mar 3;22(1):60. doi: 10.1186/s12974-025-03371-0.
Alzheimer's disease (AD) is the most common neurodegenerative disease worldwide. Amyloid-β (Aβ) accumulation and neurofibrillary tangles are two key histological features resulting in progressive and irreversible neuronal loss and cognitive decline. The macrophages of the central nervous system (CNS) belong to the innate immune system and comprise parenchymal microglia and CNS-associated macrophages (CAMs) at the CNS interfaces (leptomeninges, perivascular space and choroid plexus). Microglia and CAMs have received attention as they may play a key role in disease onset and progression e. g., by clearing amyloid beta (Aβ) through phagocytosis. Genome-wide association studies (GWAS) have revealed that human microglia and CAMs express numerous risk genes for AD, further highlighting their potentially critical role in AD pathogenesis. Microglia and CAMs are tightly controlled by environmental factors, such as the host microbiota. Notably, it was further reported that the composition of the gut microbiota differed between AD patients and healthy individuals. Hence, emerging studies have analyzed the impact of gut bacteria in different preclinical mouse models for AD as well as in clinical studies, potentially enabling promising new therapeutic options.
阿尔茨海默病(AD)是全球最常见的神经退行性疾病。淀粉样β蛋白(Aβ)的积累和神经纤维缠结是导致神经元进行性不可逆丧失和认知能力下降的两个关键组织学特征。中枢神经系统(CNS)的巨噬细胞属于固有免疫系统,包括脑实质小胶质细胞和位于CNS界面(软脑膜、血管周围间隙和脉络丛)的CNS相关巨噬细胞(CAMs)。小胶质细胞和CAMs受到关注,因为它们可能在疾病的发生和发展中起关键作用,例如通过吞噬作用清除淀粉样β蛋白(Aβ)。全基因组关联研究(GWAS)表明,人类小胶质细胞和CAMs表达众多AD风险基因,进一步凸显了它们在AD发病机制中潜在的关键作用。小胶质细胞和CAMs受到环境因素的严格调控,如宿主微生物群。值得注意的是,进一步报道显示AD患者和健康个体的肠道微生物群组成存在差异。因此,新出现的研究分析了肠道细菌在不同AD临床前小鼠模型以及临床研究中的影响,这可能带来有前景的新治疗选择。