Burns K, Clatworthy J, Martin L, Martinon F, Plumpton C, Maschera B, Lewis A, Ray K, Tschopp J, Volpe F
Institute of Biochemistry, University of Lausanne, BIL Biomedical Research centre, Chemin des Boveresses 155, CH-1066 Epalinges, Switzerland.
Nat Cell Biol. 2000 Jun;2(6):346-51. doi: 10.1038/35014038.
Interleukin-1 (IL-1) is a proinflammatory cytokine that elicits its pleiotropic effects through activation of the transcription factors NF-kappaB and AP-1. Binding of IL-1 to its receptor results in rapid assembly of a membrane-proximal signalling complex that consists of two different receptor chains (IL-1Rs), IL-1RI and IL-1RAcP, the adaptor protein MyD88, the serine/threonine kinase IRAK and a new protein, which we have named Tollip. Here we show that, before IL-1beta treatment, Tollip is present in a complex with IRAK, and that recruitment of Tollip-IRAK complexes to the activated receptor complex occurs through association of Tollip with IL-1RAcP. Co-recruited MyD88 then triggers IRAK autophosphorylation, which in turn leads to rapid dissociation of IRAK from Tollip (and IL-1Rs). As overexpression of Tollip results in impaired NF-kappaB activation, we conclude that Tollip is an important constituent of the IL-1R signalling pathway.
白细胞介素-1(IL-1)是一种促炎细胞因子,它通过激活转录因子NF-κB和AP-1发挥其多效性作用。IL-1与其受体结合会导致膜近端信号复合物的快速组装,该复合物由两条不同的受体链(IL-1Rs)、IL-1RI和IL-1RAcP、衔接蛋白MyD88、丝氨酸/苏氨酸激酶IRAK以及一种我们命名为Tollip的新蛋白组成。我们在此表明,在IL-1β处理之前,Tollip与IRAK存在于一个复合物中,并且Tollip-IRAK复合物向活化受体复合物的募集是通过Tollip与IL-1RAcP的结合实现的。随后共同募集的MyD88触发IRAK的自磷酸化,这进而导致IRAK从Tollip(和IL-1Rs)迅速解离。由于Tollip的过表达导致NF-κB激活受损,我们得出结论,Tollip是IL-1R信号通路的重要组成部分。