Mindrescu Catalin, Le Junming, Wisniewski Hans-Georg, Vilcek Jan
Department of Microbiology, New York University School of Medicine, New York, USA.
Biochem Biophys Res Commun. 2005 May 13;330(3):737-45. doi: 10.1016/j.bbrc.2005.03.040.
TNF-stimulated gene 6 (TSG-6) encodes a 35 kDa inducible secreted glycoprotein important in inflammation and female fertility. Previous studies have shown that TSG-6 has anti-inflammatory activity in models of acute and chronic inflammation. In the present study, we show that treatment of the RAW 264.7 murine macrophage cell line with TSG-6 protein up-regulates the expression of inducible cyclooxygenase-2 (COX-2), a key enzyme in inflammation and immune responses. This action of TSG-6 protein was abolished by heat denaturation, trypsin digestion, or anti-TSG-6 antibodies. TSG-6 treatment also resulted in a rapid increase in COX-2 mRNA levels, suggesting that TSG-6 up-regulates COX-2 gene expression. Up-regulation of COX-2 was accompanied by an increase in the production of prostaglandins, especially PGD2. As the PGD2 metabolite, 15-deoxy-Delta12,14-PGJ2, can act as a negative regulator of inflammation, these TSG-6 actions may explain, at least in part, the anti-inflammatory effect of TSG-6 observed in the intact organism.
肿瘤坏死因子刺激基因6(TSG-6)编码一种35 kDa的可诱导分泌糖蛋白,在炎症和女性生育中起重要作用。先前的研究表明,TSG-6在急性和慢性炎症模型中具有抗炎活性。在本研究中,我们发现用TSG-6蛋白处理RAW 264.7小鼠巨噬细胞系可上调诱导型环氧化酶-2(COX-2)的表达,COX-2是炎症和免疫反应中的关键酶。TSG-6蛋白的这一作用可通过热变性、胰蛋白酶消化或抗TSG-6抗体消除。TSG-6处理还导致COX-2 mRNA水平迅速升高,表明TSG-6上调了COX-2基因表达。COX-2的上调伴随着前列腺素尤其是PGD2产生的增加。由于PGD2代谢产物15-脱氧-Δ12,14-PGJ2可作为炎症的负调节剂,这些TSG-6的作用可能至少部分解释了在完整生物体中观察到的TSG-6的抗炎作用。