Glycanogenomics: A qPCR-approach to investigate biological glycan function

被引:21
作者
Krenn, Evelyn C. [1 ]
Wille, Iris [1 ]
Gesslbauer, Bernd [1 ]
Poteser, Michael [2 ]
van Kuppevelt, Toin H. [3 ]
Kungl, Andreas J. [1 ,4 ]
机构
[1] Graz Univ, Dept Pharmaceut Chem, Inst Pharmaceut Sci, A-8010 Graz, Austria
[2] Graz Univ, Dept Pharmaceut Sci, A-8010 Graz, Austria
[3] Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Biochem, NL-6500 HB Nijmegen, Netherlands
[4] ProtAffin Biotechnol AG, A-8020 Graz, Austria
关键词
heparan sulfate; endothelium; inflammation; TNF-alpha; N-deacetylase/N-sulfotransferase; 3-O-sulfotransferase; real-time PCR;
D O I
10.1016/j.bbrc.2008.07.144
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As an indirect approach towards glycan structures, qRT-PCR analyses using the Delta Delta C-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. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:297 / 302
页数:6
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