Krenn Evelyn C, Wille Iris, Gesslbauer Bernd, Poteser Michael, van Kuppevelt Toin H, Kungl Andreas J
Institute for Pharmaceutical Sciences, Department of Pharmaceutical Chemistry, University of Graz, Universitätsplatz 1, A-8010 Graz, Austria.
Biochem Biophys Res Commun. 2008 Oct 24;375(3):297-302. doi: 10.1016/j.bbrc.2008.07.144. Epub 2008 Aug 8.
As an indirect approach towards glycan structures, qRT-PCR analyses using the DeltaDeltaC(T) method were performed to investigate changes in expression levels of heparan sulfate-synthesising enzymes of stimulated and unstimulated HMVECs. We chose NDSTs as early enzymes initiating sulfation and 3OSTs which act late generating specific binding sites. Major changes in expression patterns were found for the NDST3 and 3OST1 isoforms. Both enzymes were down-regulated 7- and 6-fold, respectively, following TNF-alpha stimulation, and 3.5- and 7.6-fold following LPS-stimulation suggesting a common restructuring process of HS in inflammation leading to a less diverse sulfation pattern. Immunostaining of TNF-alpha-stimulated cells using a phage display-derived antibody specific for 3-O-sulfation and unsulfated regions of HS resulted in significant fluorescence changes between unstimulated and stimulated.
作为一种研究聚糖结构的间接方法,采用ΔΔC(T)法进行qRT-PCR分析,以研究刺激和未刺激的人微血管内皮细胞(HMVECs)中硫酸乙酰肝素合成酶表达水平的变化。我们选择硫酸乙酰肝素N-硫酸转移酶(NDSTs)作为启动硫酸化的早期酶,以及硫酸转移酶3(3OSTs)作为后期产生特定结合位点的酶。在硫酸乙酰肝素N-硫酸转移酶3(NDST3)和硫酸转移酶3-1(3OST1)亚型中发现了表达模式的主要变化。在肿瘤坏死因子-α(TNF-α)刺激后,这两种酶分别下调了7倍和6倍,在脂多糖(LPS)刺激后分别下调了3.5倍和7.6倍,这表明炎症中硫酸乙酰肝素(HS)存在一个共同的重组过程,导致硫酸化模式的多样性降低。使用针对硫酸乙酰肝素3-O-硫酸化和未硫酸化区域的噬菌体展示衍生抗体对TNF-α刺激的细胞进行免疫染色,结果显示未刺激和刺激细胞之间存在显著的荧光变化。