Department of Immunology and Cell Biology, Cancer Research Pavilion, Faculty of Medicine and Health Sciences, Université de Sherbrooke, 3201, rue Jean Mignault, Sherbrooke, QC, J1E4K8, Canada.
Cell Commun Signal. 2021 Jan 25;19(1):10. doi: 10.1186/s12964-020-00693-9.
Over the past 2 decades, pattern recognition receptors (PRRs) have been shown to be on the front line of many illnesses such as autoimmune, inflammatory, and neurodegenerative diseases as well as allergies and cancer. Among PRRs, toll-like receptors (TLRs) are the most studied family. Dissecting TLRs signaling turned out to be advantageous to elaborate efficient treatments to cure autoimmune and chronic inflammatory disorders. However, a broad understanding of TLR effectors is required to propose a better range of cures. In addition to kinases and E3 ubiquitin ligases, phosphatases emerge as important regulators of TLRs signaling mediated by NF-κB, type I interferons (IFN I) and Mitogen-Activated Protein Kinases signaling pathways. Here, we review recent knowledge on TLRs signaling modulation by different classes and subclasses of phosphatases. Thus, it becomes more and more evident that phosphatases could represent novel therapeutic targets to control pathogenic TLRs signaling. Video Abstract.
在过去的 20 年中,模式识别受体(PRRs)已被证明处于许多疾病的前沿,如自身免疫、炎症和神经退行性疾病以及过敏和癌症。在 PRRs 中, Toll 样受体(TLRs)是研究最多的家族。对 TLRs 信号的剖析被证明有利于制定有效的治疗方法来治疗自身免疫和慢性炎症性疾病。然而,需要广泛了解 TLR 效应物,才能提出更好的治疗方案。除了激酶和 E3 泛素连接酶外,磷酸酶作为 NF-κB、I 型干扰素(IFN I)和丝裂原激活蛋白激酶信号通路介导的 TLRs 信号的重要调节剂而出现。在这里,我们综述了不同类别和子类的磷酸酶对 TLRs 信号转导的调节的最新知识。因此,越来越明显的是,磷酸酶可能代表控制致病 TLRs 信号的新型治疗靶标。视频摘要。