Baylor Institute for Immunology Research, Baylor Research Institute, Baylor Health Care System, Dallas, TX 75204, USA.
Immunity. 2013 Jul 25;39(1):123-35. doi: 10.1016/j.immuni.2013.07.001. Epub 2013 Jul 18.
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.
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。