Beauchef Gallic, Kypriotou Magdalini, Chadjichristos Christos, Widom Russell L, Porée Benoît, Renard Emmanuelle, Moslemi Safa, Wegrowski Yanusz, Maquart François-Xavier, Pujol Jean-Pierre, Galéra Philippe
Laboratory of Connective Tissue Biochemistry, Faculty of Medicine, Caen, France.
Biochem Biophys Res Commun. 2005 Aug 12;333(4):1123-31. doi: 10.1016/j.bbrc.2005.06.020.
Chondrocyte glycosaminoglycan (GAG) synthesis is regulated by the availability of UDP-glucuronate, the substrate of glucuronosyl transferases which form the GAG chains in proteoglycans and hyaluronan. UDP-glucose dehydrogenase (UDPGD) is therefore a key enzyme in the synthesis of UDP-glucuronate from glucose. However, the mechanisms regulating its expression in chondrocytes are not fully understood. We investigated the effect of c-Krox, a zinc-finger transcription factor previously shown to modulate several matrix genes, on the synthesis of GAG and transcriptional activity of several UDPGD gene promoter constructs, using transient transfection and decoy experiments in rabbit articular chondrocytes (RACs). We show that overexpression of c-Krox inhibits radiosulfate incorporation into neosynthesized GAG and that the effect was mediated by a cis-sequence located between +18 and +39bp of the UDPGD gene. Since that sequence can also bind Sp1/Sp3 factors, it is likely that c-Krox acts in concert with these proteins to modulate the UDPGD gene expression in articular chondrocytes.
软骨细胞糖胺聚糖(GAG)的合成受UDP-葡萄糖醛酸可用性的调节,UDP-葡萄糖醛酸是葡萄糖醛酸基转移酶的底物,该酶在蛋白聚糖和透明质酸中形成GAG链。因此,UDP-葡萄糖脱氢酶(UDPGD)是从葡萄糖合成UDP-葡萄糖醛酸的关键酶。然而,调节其在软骨细胞中表达的机制尚未完全了解。我们使用兔关节软骨细胞(RACs)的瞬时转染和诱饵实验,研究了c-Krox(一种先前显示可调节多个基质基因的锌指转录因子)对GAG合成和几种UDPGD基因启动子构建体转录活性的影响。我们发现,c-Krox的过表达抑制了放射性硫酸盐掺入新合成的GAG中,并且该效应由UDPGD基因+18至+39bp之间的顺式序列介导。由于该序列也可以结合Sp1/Sp3因子,因此c-Krox可能与这些蛋白质协同作用,以调节关节软骨细胞中UDPGD基因的表达。