Discipline of Physiology, School of Medicine, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, Ireland.
Discipline of Physiology, School of Medicine, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, Ireland; Transpharmation Ireland Limited, Institute of Neuroscience, Trinity College, Dublin 2, Ireland.
Biochem Pharmacol. 2024 Apr;222:116082. doi: 10.1016/j.bcp.2024.116082. Epub 2024 Mar 2.
Toll-like receptors (TLRs) have become a focus in biomedicine and biomedical research given the roles of this unique family of innate immune proteins in immune activation, infection, and autoimmunity. It is evident that TLR dysregulation, and subsequent alterations in TLR-mediated inflammatory signalling, can contribute to disease pathogenesis, and TLR targeted therapies are in development. This review highlights evidence that cannabinoids are key regulators of TLR signalling. Cannabinoids include component of the plant Cannabis sativa L. (C. sativa), synthetic and endogenous ligands, and overall represent a class of compounds whose therapeutic potential and mechanism of action continues to be elucidated. Cannabinoid-based medicines are in the clinic, and are furthermore under intense investigation for broad clinical development to manage symptoms of a range of disorders. In this review, we present an overview of research evidence that signalling linked to a range of TLRs is targeted by cannabinoids, and such cannabinoid mediated effects represent therapeutic avenues for further investigation. First, we provide an overview of TLRs, adaptors and key signalling events, alongside a summary of evidence that TLRs are linked to disease pathologies. Next, we discuss the cannabinoids system and the development of cannabinoid-based therapeutics. Finally, for the bulk of this review, we systematically outline the evidence that cannabinoids (plant-derived cannabinoids, synthetic cannabinoids, and endogenous cannabinoid ligands) can cross-talk with innate immune signalling governed by TLRs, focusing specifically on each member of the TLR family. Cannabinoids should be considered as key regulators of signalling controlled by TLRs, and such regulation should be a major focus in terms of the anti-inflammatory propensity of the cannabinoid system.
Toll 样受体 (TLRs) 已成为生物医学和生物医学研究的焦点,因为该家族独特的先天免疫蛋白在免疫激活、感染和自身免疫中具有重要作用。显然,TLR 失调以及随后 TLR 介导的炎症信号改变可能导致疾病发病机制,并且正在开发 TLR 靶向疗法。这篇综述强调了证据表明大麻素是 TLR 信号的关键调节剂。大麻素包括植物大麻 sativa L.(C. sativa)的成分、合成和内源性配体,总体上代表了一类化合物,其治疗潜力和作用机制仍在阐明中。基于大麻素的药物已在临床中使用,并且正在进行广泛的临床开发研究,以治疗一系列疾病的症状。在这篇综述中,我们概述了研究证据,表明大麻素靶向与一系列 TLR 相关的信号,并且这种大麻素介导的作用代表了进一步研究的治疗途径。首先,我们概述了 TLRs、衔接蛋白和关键信号事件,并总结了 TLRs 与疾病病理相关的证据。接下来,我们讨论了大麻素系统和大麻素为基础的治疗方法的发展。最后,在这篇综述的大部分内容中,我们系统地概述了证据,表明大麻素(植物衍生的大麻素、合成大麻素和内源性大麻素配体)可以与 TLR 调节的先天免疫信号相互作用,特别关注 TLR 家族的每个成员。大麻素应被视为 TLR 控制的信号的关键调节剂,并且这种调节应该是大麻素系统抗炎倾向的主要重点。