Hoff Norman-Philipp, Degrandi Daniel, Hengge Ulrich, Pfeffer Klaus, Wurthner Jens Ulrich
Institute for Medical Microbiology, University of Duesseldorf, 40225, Duesseldorf, Germany.
J Clin Immunol. 2007 Nov;27(6):568-79. doi: 10.1007/s10875-007-9118-7. Epub 2007 Jul 20.
Transforming growth factor-beta (TGF-beta) is a multifunctional cytokine that mainly acts as an inhibitor of immune functions. A lack of functional TGF-beta leads to autoimmune disease in animal models and dysregulated TGF-beta signaling is implicated in human autoimmune diseases. To define target genes that play a part in the inhibitory role of TGF-beta in the immune system, we have identified genes stimulated by TGF-beta in macrophages by gene-chip analysis. One of the TGF-beta regulated genes is carboxypeptidase D (CpD), a 180-kDa type I membrane protein. We have demonstrated that CpD is regulated by TGF-beta in various cell types of both, murine and human origin and, interestingly, is significantly downregulated in CD14 positive cells isolated from patients with lupus erythematosus (LE). Moreover, we show that downregulation of CpD leads to downmodulation of TGF-beta itself, suggesting a role for CpD in a positive feedback loop, providing further evidence for a role of this enzyme in LE. To our knowledge, this is the first report that demonstrates carboxypeptidase D as a TGF-beta target gene that is implicated in the pathogenesis of LE.
转化生长因子-β(TGF-β)是一种多功能细胞因子,主要作为免疫功能的抑制剂发挥作用。在动物模型中,功能性TGF-β的缺乏会导致自身免疫性疾病,而TGF-β信号失调与人类自身免疫性疾病有关。为了确定在免疫系统中参与TGF-β抑制作用的靶基因,我们通过基因芯片分析鉴定了巨噬细胞中受TGF-β刺激的基因。TGF-β调节的基因之一是羧肽酶D(CpD),一种180 kDa的I型膜蛋白。我们已经证明,CpD在源自小鼠和人类的多种细胞类型中受TGF-β调节,有趣的是,在从红斑狼疮(LE)患者分离的CD14阳性细胞中显著下调。此外,我们表明CpD的下调导致TGF-β本身的下调,提示CpD在正反馈回路中发挥作用,为该酶在LE中的作用提供了进一步的证据。据我们所知,这是第一份证明羧肽酶D作为与LE发病机制相关的TGF-β靶基因的报告。