TLR4 内源性配体在小胶质细胞中的作用:相关神经疾病的潜在靶点。
Endogenous Ligands of TLR4 in Microglia: Potential Targets for Related Neurological Diseases.
机构信息
School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, P.R. China.
Office of China National Narcotics Control Commission, China Pharmaceutical University, Joint Laboratory on Key Technologies of Narcotics Control, Nanjing, 210009, P.R. China.
出版信息
Curr Drug Targets. 2024;25(14):953-970. doi: 10.2174/0113894501316051240821060249.
Chronic inflammation mediated by microglia is a cause of some neuroinflammatory diseases. TLR4, a natural immune receptor on microglia, plays an important role in the occurrence of inflammation and the process of diseases. TLR4 can be activated by a variety of ligands to trigger inflammatory responses, including endogenous ligands HMGB1, S100A8/9, Heme, and Fetuin-A. As ligands derived from the body itself, they have the ability to bind directly to TLR4 and can be used as inducers of aseptic inflammation. In the past 20 years, targeting ligands rather than receptors has become an emerging therapeutic strategy for the treatment of diseases, so understanding the relationship between microglia, TLR4, TLR4 ligands, and corresponding diseases may have new implications for the treatment of diseases. In the article, we will discuss the TLR4 and the endogenous substances that can activate the TLR4 signaling pathway and present literature support for their role in neuroinflammatory diseases.
小胶质细胞介导的慢性炎症是一些神经炎症性疾病的病因。TLR4 是小胶质细胞上的天然免疫受体,在炎症的发生和疾病的进展过程中起着重要作用。TLR4 可以被多种配体激活,从而引发炎症反应,包括内源性配体 HMGB1、S100A8/9、血红素和胎球蛋白-A。作为源自于身体自身的配体,它们能够直接与 TLR4 结合,并可作为无菌性炎症的诱导剂。在过去的 20 年中,靶向配体而非受体已成为治疗疾病的一种新兴治疗策略,因此,了解小胶质细胞、TLR4、TLR4 配体以及相应疾病之间的关系,可能对疾病的治疗具有新的意义。在本文中,我们将讨论 TLR4 以及能够激活 TLR4 信号通路的内源性物质,并为它们在神经炎症性疾病中的作用提供文献支持。