School of Medicine, Tehran University of Medical Sciences, Tehran, Iran; Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
School of Medicine, Tehran University of Medical Sciences, Tehran, Iran; Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran; Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
Pharmacol Res. 2022 Jan;175:105960. doi: 10.1016/j.phrs.2021.105960. Epub 2021 Oct 28.
Diabetic retinopathy (DR) is the most frequent microvascular complication of diabetes mellitus (DM) and a leading cause of blindness worldwide. Evidence has shown that DR is an inflammatory disease with hyperglycemia playing a causative role in the development of its main features, including inflammation, cellular apoptosis, neurodegeneration, oxidative stress, and neovascularization. Toll-like receptors (TLRs) are a well-known family of pattern recognition receptors (PRRs) responsible for the initiation of inflammatory and immune responses. TLR4 identifies both endogenous and exogenous ligands and is associated with various physiological and pathological pathways in the body. While the detailed pathophysiology of DR is still unclear, increasing data suggests a crucial role for TLR4 in the development of DR. Due to hyperglycemia, TLR4 expression increases in diabetic retina, which activates various pathways leading to DR. Considering the role of TLR4 in DR, several studies have focused on the association of TLR4 polymorphisms and risk of DR development. Moreover, evidence concerning the effect of microRNAs in the pathogenesis of DR, through their interaction with TLR4, indicates the determinant role of TLR4 in this disease. Of note, several agents have proven as effective in alleviating DR through the inhibition of the TLR4 pathway, suggesting new avenues in DR treatment. In this review, we provided a brief overview of the TLR4 structure and biological function and a more comprehensive discussion about the mechanisms of TLR4 activation in DR. Furthermore, we summarized the relationship between TLR4 polymorphisms and risk of DR and the relationship between microRNAs and TLR4 in DR. Finally, we discussed the current progress in designing TLR4 inhibitors, which could be helpful in DR clinical management.
糖尿病视网膜病变 (DR) 是糖尿病 (DM) 最常见的微血管并发症,也是全球致盲的主要原因。有证据表明,DR 是一种炎症性疾病,高血糖在其主要特征(包括炎症、细胞凋亡、神经退行性变、氧化应激和新生血管形成)的发展中起致病作用。Toll 样受体 (TLR) 是一组已知的模式识别受体 (PRR),负责启动炎症和免疫反应。TLR4 识别内源性和外源性配体,与体内各种生理和病理途径相关。虽然 DR 的详细病理生理学仍不清楚,但越来越多的数据表明 TLR4 在 DR 的发展中起着至关重要的作用。由于高血糖,糖尿病视网膜中 TLR4 的表达增加,这激活了导致 DR 的各种途径。鉴于 TLR4 在 DR 中的作用,一些研究集中在 TLR4 多态性与 DR 发展风险的关联上。此外,关于 microRNAs 通过与 TLR4 相互作用在 DR 发病机制中的作用的证据表明 TLR4 在该疾病中的决定性作用。值得注意的是,几种通过抑制 TLR4 途径证明对缓解 DR 有效的药物表明,DR 的治疗有了新的途径。在这篇综述中,我们简要概述了 TLR4 的结构和生物学功能,并更全面地讨论了 TLR4 在 DR 中的激活机制。此外,我们总结了 TLR4 多态性与 DR 风险的关系以及 microRNAs 与 DR 中 TLR4 的关系。最后,我们讨论了设计 TLR4 抑制剂的最新进展,这可能有助于 DR 的临床管理。