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DHX33 RNA 解旋酶感知细胞质 RNA 并激活 NLRP3 炎性体。

The DHX33 RNA helicase senses cytosolic RNA and activates the NLRP3 inflammasome.

机构信息

Baylor Institute for Immunology Research, Baylor Research Institute, Baylor Health Care System, Dallas, TX 75204, USA.

出版信息

Immunity. 2013 Jul 25;39(1):123-35. doi: 10.1016/j.immuni.2013.07.001. Epub 2013 Jul 18.

Abstract

The NLRP3 inflammasome plays a major role in innate immune responses by activating caspase-1, resulting in secretion of interleukin-18 (IL-18) and IL-1β. Although cytosolic double-stranded RNA (dsRNA) and bacterial RNA are known to activate the NLRP3 inflammasome, the upstream sensor is unknown. We investigated the potential function of DExD/H-box RNA helicase family members (previously shown to sense cytosolic DNA and RNA to induce type 1 interferon responses) in RNA-induced NLRP3 inflammasome activation. Among the helicase family members tested, we found that targeting of DHX33 expression by short hairpin RNA efficiently blocked the activation of caspase-1 and secretion of IL-18 and IL-1β in human macrophages that were activated by cytosolic poly I:C, reoviral RNA, or bacterial RNA. DHX33 bound dsRNA via the helicase C domain. DHX33 interacted with NLRP3 and formed the inflammasome complex following stimulation with RNA. We therefore identified DHX33 as a cytosolic RNA sensor that activates the NLRP3 inflammasome.

摘要

NLRP3 炎性小体通过激活半胱天冬酶-1在先天免疫反应中起主要作用,导致白细胞介素-18(IL-18)和白细胞介素-1β的分泌。虽然已知细胞质双链 RNA(dsRNA)和细菌 RNA 能够激活 NLRP3 炎性小体,但上游传感器尚不清楚。我们研究了 DExD/H 框 RNA 解旋酶家族成员(先前显示能够感应细胞质 DNA 和 RNA 以诱导 I 型干扰素反应)在 RNA 诱导的 NLRP3 炎性小体激活中的潜在作用。在测试的解旋酶家族成员中,我们发现短发夹 RNA 靶向 DHX33 的表达可有效阻断人巨噬细胞中 caspase-1 的激活和 IL-18 和 IL-1β 的分泌,这些巨噬细胞被细胞质多聚 I:C、肠道病毒 RNA 或细菌 RNA 激活。DHX33 通过解旋酶 C 结构域与 dsRNA 结合。DHX33 与 NLRP3 相互作用,并在 RNA 刺激后形成炎性小体复合物。因此,我们确定 DHX33 为激活 NLRP3 炎性小体的细胞质 RNA 传感器。

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