Center for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
J Immunol. 2011 Feb 1;186(3):1369-76. doi: 10.4049/jimmunol.1002047. Epub 2010 Dec 27.
Repulsive guidance molecule (RGM) family members RGMa, RGMb/Dragon, and RGMc/hemojuvelin were found recently to act as bone morphogenetic protein (BMP) coreceptors that enhance BMP signaling activity. Although our previous studies have shown that hemojuvelin regulates hepcidin expression and iron metabolism through the BMP pathway, the role of the BMP signaling mediated by Dragon remains largely unknown. We have shown previously that Dragon is expressed in neural cells, germ cells, and renal epithelial cells. In this study, we demonstrate that Dragon is highly expressed in macrophages. Studies with RAW264.7 and J774 macrophage cell lines reveal that Dragon negatively regulates IL-6 expression in a BMP ligand-dependent manner via the p38 MAPK and Erk1/2 pathways but not the Smad1/5/8 pathway. We also generated Dragon knockout mice and found that IL-6 is upregulated in macrophages and dendritic cells derived from whole lung tissue of these mice compared with that in respective cells derived from wild-type littermates. These results indicate that Dragon is an important negative regulator of IL-6 expression in immune cells and that Dragon-deficient mice may be a useful model for studying immune and inflammatory disorders.
排斥性导向分子(RGM)家族成员 RGMa、RGMb/Dragon 和 RGMc/hemojuvelin 最近被发现作为骨形态发生蛋白(BMP)的辅助受体,增强 BMP 信号活性。尽管我们之前的研究表明 hemojuvelin 通过 BMP 途径调节铁调素的表达和铁代谢,但 Dragon 介导的 BMP 信号的作用在很大程度上仍然未知。我们之前已经表明,Dragon 在神经细胞、生殖细胞和肾上皮细胞中表达。在这项研究中,我们证明 Dragon 在巨噬细胞中高度表达。对 RAW264.7 和 J774 巨噬细胞系的研究表明,Dragon 通过 p38 MAPK 和 Erk1/2 途径而非 Smad1/5/8 途径负调控 BMP 配体依赖性的 IL-6 表达。我们还生成了 Dragon 敲除小鼠,并发现与野生型同窝小鼠的相应细胞相比,这些小鼠的整个肺组织来源的巨噬细胞和树突状细胞中的 IL-6 上调。这些结果表明,Dragon 是免疫细胞中 IL-6 表达的重要负调节剂,Dragon 缺陷小鼠可能是研究免疫和炎症性疾病的有用模型。