Dowds Theresa A, Masumoto Junya, Chen Felicia F, Ogura Yasunori, Inohara Naohiro, Núñez Gabriel
Department of Pathology and Comprehensive Cancer Center, The University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Biochem Biophys Res Commun. 2003 Mar 14;302(3):575-80. doi: 10.1016/s0006-291x(03)00221-3.
Cryopyrin, a member of the Nod protein family mutated in familial cold urticaria and Muckle-Wells syndrome, has been recently implicated in inflammation. However, the mechanism of activation and regulation of the cryopyrin signaling pathway remains poorly understood. We report here that co-expression of cryopyrin with its binding partner, ASC, induced both apoptosis and NF-kappaB activation. This signaling was mimicked by oligomerization of ASC, suggesting that cryopyrin activates downstream targets as reported for other Nod family members. Notably, pyrin, the product of the familial Mediterranean fever gene, inhibited cryopyrin-mediated apoptosis and NF-kappaB activation by disrupting the cryopyrin-ASC interaction. These results provide evidence for a cryopyrin signaling pathway activated through the induced proximity of ASC, which is negatively regulated by pyrin.
冷吡啉是家族性寒冷性荨麻疹和穆克勒-韦尔斯综合征中发生突变的Nod蛋白家族成员之一,最近被认为与炎症有关。然而,冷吡啉信号通路的激活和调节机制仍知之甚少。我们在此报告,冷吡啉与其结合伴侣ASC共表达可诱导细胞凋亡和NF-κB激活。ASC的寡聚化模拟了这种信号传导,表明冷吡啉如其他Nod家族成员一样激活下游靶点。值得注意的是,家族性地中海热基因的产物吡啉通过破坏冷吡啉-ASC相互作用,抑制冷吡啉介导的细胞凋亡和NF-κB激活。这些结果为通过诱导ASC接近而激活的冷吡啉信号通路提供了证据,该通路受到吡啉的负调节。