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The interleukin-1 receptor/Toll-like receptor superfamily: 10 years of progress.

机译:白细胞介素1受体/ Toll样受体超家族:10年的发展。

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The interleukin-1 receptor (IL-1R)/Toll-like receptor (TLR) superfamily was first defined in 1998 as a family of proteins that contain the Toll-IL-1 receptor domain. At that time, there were a number of orphan receptors in the IL-1R branch, and the TLRs had yet to be shown to be key innate immune receptors that sense microbial products. We now know a great deal more about this superfamily, with the description of novel IL-1 family members such as IL-1F6 signaling via IL-1Rrp2 and IL33 signaling via ST2. Remarkable progress has been made in our understanding of the functions of the TLRs, leading to a renaissance of interest in innate immunity. The importance of IL-1 is also being rediscovered, with the observation that Nalp3 is a key regulator of caspase-1, the enzyme that processes pro-IL-1beta into the mature cytokine. This area has therefore proved very fruitful in terms of improving our knowledge of the molecular basis for innate immunity and inflammation, and we can anticipate further discoveries in the coming years.
机译:白介素-1受体(IL-1R)/ Toll样受体(TLR)超家族于1998年首次定义为包含Toll-IL-1受体域的蛋白质家族。当时,IL-1R分支中有许多孤儿受体,而且尚未证明TLR是检测微生物产物的关键先天免疫受体。现在,我们通过描述新的IL-1家族成员,例如通过IL-1Rrp2的IL-1F6信号和通过ST2的IL33信号,对这个超家族有了更多了解。在我们对TLR的功能的理解上取得了显着进展,从而引起了人们对先天免疫的兴趣的复兴。 IL-1的重要性也在重新发现,因为观察到Nalp3是caspase-1的关键调节剂,该酶将pro-IL-1beta加工成成熟的细胞因子。因此,在提高我们对先天免疫和炎症的分子基础的认识方面,这一领域被证明是非常富有成果的,并且我们可以预见在未来的几年中将有更多发现。

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