Sarkar Anasuya, Duncan Michelle, Hart Judy, Hertlein Erin, Guttridge Denis C, Wewers Mark D
Davis Heart and Lung Research Institute, The Ohio State University, Columbus 43210, USA.
J Immunol. 2006 Apr 15;176(8):4979-86. doi: 10.4049/jimmunol.176.8.4979.
Receptor interacting protein-2 (RIP2) is a caspase recruitment domain (CARD)-containing kinase that interacts with caspase-1 and plays an important role in NF-kappaB activation. Apoptosis-associated speck-like protein containing a CARD (ASC) is a PYRIN and CARD-containing molecule, important in the induction of apoptosis and caspase-1 activation. Although RIP2 has also been linked to caspase-1 activation, RIP2 knockout animals fail to show a defect in caspase-1-mediated processing of proIL-1beta to its active form. Therefore, RIP2 function in binding to caspase-1 remains poorly understood. We hypothesized that caspase-1 may serve as a scaffolding molecule that promotes RIP2 interaction with IkappaB kinase-gamma thus inducing NF-kappaB activation. We further hypothesized that ASC, which also interacts with caspase-1 via its CARD, may interfere with the caspase-1 RIP2 interaction. In HEK293 cells, ASC induced prominent activation of caspase-1 and proIL-1beta processing. RIP2 transient transfection induced transcription of an NF-kappaB reporter gene. This RIP2-induced NF-kappaB activity and caspase-1 binding was inhibited in a dose-dependent fashion by ASC. Consistent with a role for caspase-1 as a scaffold for RIP2, caspase-1 knockout macrophages were suppressed in their ability to activate NF-kappaB, and septic caspase-1 knockout animals produced less IL-6, a functional marker of NF-kappaB activity. Lastly, THP-1 cells treated with small interfering RNA for ASC decreased their caspase-1 activity while enhancing their NF-kappaB signal. These data suggest that ASC may direct caspase-1 away from RIP2-mediated NF-kappaB activation, toward caspase-1-mediated processing of proIL-1beta by interfering with the RIP2 caspase-1 interaction.
受体相互作用蛋白2(RIP2)是一种含半胱天冬酶募集结构域(CARD)的激酶,它与半胱天冬酶-1相互作用,并在核因子κB(NF-κB)激活中发挥重要作用。含CARD的凋亡相关斑点样蛋白(ASC)是一种含PYRIN和CARD的分子,在凋亡诱导和半胱天冬酶-1激活中起重要作用。尽管RIP2也与半胱天冬酶-1激活有关,但RIP2基因敲除动物在半胱天冬酶-1介导的前白细胞介素-1β加工成其活性形式方面未表现出缺陷。因此,RIP2与半胱天冬酶-1结合的功能仍知之甚少。我们推测半胱天冬酶-1可能作为一种支架分子,促进RIP2与IκB激酶γ相互作用,从而诱导NF-κB激活。我们进一步推测,同样通过其CARD与半胱天冬酶-1相互作用的ASC可能会干扰半胱天冬酶-1与RIP2的相互作用。在人胚肾293细胞中,ASC诱导了半胱天冬酶-1的显著激活和前白细胞介素-1β的加工。RIP2瞬时转染诱导了NF-κB报告基因的转录。ASC以剂量依赖的方式抑制了这种RIP2诱导的NF-κB活性和半胱天冬酶-1结合。与半胱天冬酶-1作为RIP2支架的作用一致,半胱天冬酶-1基因敲除巨噬细胞激活NF-κB的能力受到抑制,脓毒症半胱天冬酶-1基因敲除动物产生较少的白细胞介素-6,这是NF-κB活性的一个功能标志物。最后,用针对ASC的小干扰RNA处理的人单核细胞白血病细胞系THP-1细胞降低了其半胱天冬酶-1活性,同时增强了其NF-κB信号。这些数据表明,ASC可能通过干扰RIP2与半胱天冬酶-1的相互作用,使半胱天冬酶-1从RIP2介导的NF-κB激活转向半胱天冬酶-1介导的前白细胞介素-1β加工。