Muzio M, Ni J, Feng P, Dixit V M
University of Michigan Medical School, Department of Pathology, Ann Arbor, MI 48109, USA.
Science. 1997 Nov 28;278(5343):1612-5. doi: 10.1126/science.278.5343.1612.
The interleukin-1 receptor (IL-1R) signaling pathway leads to nuclear factor kappa B (NF-kappaB) activation in mammals and is similar to the Toll pathway in Drosophila: the IL-1R-associated kinase (IRAK) is homologous to Pelle. Two additional proximal mediators were identified that are required for IL-1R-induced NF-kappaB activation: IRAK-2, a Pelle family member, and MyD88, a death domain-containing adapter molecule. Both associate with the IL-1R signaling complex. Dominant negative forms of either attenuate IL-1R-mediated NF-kappaB activation. Therefore, IRAK-2 and MyD88 may provide additional therapeutic targets for inhibiting IL-1-induced inflammation.
白细胞介素-1受体(IL-1R)信号通路可导致哺乳动物体内核因子κB(NF-κB)的激活,且与果蝇中的Toll通路相似:IL-1R相关激酶(IRAK)与Pelle同源。另外还鉴定出了IL-1R诱导的NF-κB激活所需的两种近端介质:Pelle家族成员IRAK-2和含死亡结构域的接头分子MyD88。二者均与IL-1R信号复合物相关。二者的显性负性形式均可减弱IL-1R介导的NF-κB激活。因此,IRAK-2和MyD88可能为抑制IL-1诱导的炎症提供额外的治疗靶点。