Department of Rehabilitation Medicine, The Third Hospital of Hebei Medical University, Shijiazhuang 050051, China.
Department of Pathophysiology, Hebei Medical University, Shijiazhuang 050051, China.
Mediators Inflamm. 2022 Aug 21;2022:7924199. doi: 10.1155/2022/7924199. eCollection 2022.
Alzheimer's disease (AD) is a progressive neurodegenerative disease that primarily manifests as memory deficits and cognitive impairment and has created health challenges for patients and society. In AD, amyloid -protein (A) induces Toll-like receptor 4 (TLR4) activation in microglia. Activation of TLR4 induces downstream signaling pathways and promotes the generation of proinflammatory cytokines, such as tumor necrosis factor- (TNF-), interleukin-6 (IL-6), and interleukin-1 (IL-1), which also trigger the activation of astrocytes and influence amyloid-dependent neuronal death. Therefore, TLR4 may be an important molecular target for treating AD by regulating neuroinflammation. Moreover, TLR4 regulates apoptosis, autophagy, and gut microbiota and is closely related to AD. This article reviews the role of TLR4 in the pathogenesis of AD and a range of potential therapies targeting TLR4 for AD. Elucidating the regulatory mechanism of TLR4 in AD may provide valuable clues for developing new therapeutic strategies for AD.
阿尔茨海默病(AD)是一种进行性神经退行性疾病,主要表现为记忆缺陷和认知障碍,给患者和社会带来了健康挑战。在 AD 中,淀粉样蛋白(A)诱导小胶质细胞中 Toll 样受体 4(TLR4)的激活。TLR4 的激活诱导下游信号通路,并促进促炎细胞因子的产生,如肿瘤坏死因子-(TNF-)、白细胞介素-6(IL-6)和白细胞介素-1(IL-1),这也触发星形胶质细胞的激活,并影响淀粉样蛋白依赖性神经元死亡。因此,TLR4 可能通过调节神经炎症成为治疗 AD 的重要分子靶点。此外,TLR4 调节细胞凋亡、自噬和肠道微生物群,与 AD 密切相关。本文综述了 TLR4 在 AD 发病机制中的作用以及针对 TLR4 的一系列潜在 AD 治疗方法。阐明 TLR4 在 AD 中的调节机制可能为开发 AD 的新治疗策略提供有价值的线索。