Disease-Association Analysis of an Inflammation-Related Feedback Loop

作者:Murakami Masaaki*; Harada Masaya; Kamimura Daisuke; Ogura Hideki; Okuyama Yuko; Kumai Noriko; Okuyama Azusa; Singh Rajeev; Jiang Jing Jing; Atsumi Toru; Shiraya Sayaka; Nakatsuji Yuji; Kinoshita Makoto; Kohsaka Hitoshi; Nishida Makoto; Sakoda Saburo; Miyasaka Nobuyuki; Yamaguchi Takihara Keiko; Hirano Toshio
来源:Cell Reports, 2013, 3(3): 946-959.
DOI:10.1016/j.celrep.2013.01.028

摘要

The IL-6-triggered positive feedback loop for NFkB signaling (or the IL-6 amplifier/Inflammation amplifier) was originally discovered as a synergistic-activation signal that follows IL-17/IL-6 stimulation in nonimmune cells. Subsequent results from animal models have shown that the amplifier is activated by stimulation of NFkB and STAT3 and induces chemokines and inflammation via an NF kappa B loop. However, its role in human diseases is unclear. Here, we combined two genome-wide mouse screens with SNP-based disease association studies, revealing 1,700 genes related to the IL-6 amplifier, 202 of which showed 492 indications of association with ailments beyond autoimmune diseases. We followed up on ErbB1 from our list. Blocking ErbB1 signaling suppressed the IL-6 amplifier, whereas the expression of epiregulin, an ErbB1 ligand, was higher in patients with inflammatory diseases. These results indicate that the IL-6 amplifier is indeed associated with human diseases and disorders and that the identified genes may make for potential therapeutic targets.

  • 出版日期2013-3