Dean and Betty Gallo Prostate Cancer Center and Section of Urologic Oncology, Division of Urology, Department of Surgery, the Cancer Institute of New Jersey, Robert Wood Johnson Medical School, New Brunswick, New Jersey 08903, USA.
J Biol Chem. 2010 Dec 10;285(50):39401-8. doi: 10.1074/jbc.M110.103705. Epub 2010 Oct 1.
Unlike the prototype transforming growth factor-β (TGF-β), bone morphogenetic protein-6 (BMP-6) activates macrophages. Here, we report that BMP-6 induces the expression of IL-6 in macrophages. Using overexpression and knockdown experiments, we demonstrate that BMP receptor type II and activin-like kinase-2 are necessary for IL-6 induction by BMP-6. At the intracellular level, both Smad and p38 signaling pathways are required for the induction of IL-6. The cross-talk between the two pathways occurs at the level of transcription factor GATA4 and Smad 1/4. These results, taken together, demonstrate a novel BMP-6 signaling mechanism in which both the Smad and non-Smad pathways directly interact to activate the transcription of a target gene.
与原型转化生长因子-β(TGF-β)不同,骨形态发生蛋白-6(BMP-6)可激活巨噬细胞。在这里,我们报告 BMP-6 可诱导巨噬细胞中白细胞介素-6(IL-6)的表达。通过过表达和敲低实验,我们证明 BMP 受体 II 型和激活素样激酶-2 是 BMP-6 诱导 IL-6 所必需的。在细胞内水平,Smad 和 p38 信号通路都需要诱导 IL-6。两条通路之间的串扰发生在转录因子 GATA4 和 Smad1/4 的水平。这些结果表明,存在一种新的 BMP-6 信号机制,其中 Smad 和非 Smad 通路直接相互作用以激活靶基因的转录。