首页> 美国卫生研究院文献>Biochemical Journal >UDP-glucose pyrophosphorylase: up-regulation in hypertrophic cartilage and role in hyaluronan synthesis.
【2h】

UDP-glucose pyrophosphorylase: up-regulation in hypertrophic cartilage and role in hyaluronan synthesis.

机译:UDP-葡萄糖焦磷酸化酶:在肥大软骨中上调并在透明质酸合成中起作用。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Previously, we have performed subtractive hybridization to identify genes up-regulated in hypertrophic chondrocytes of the avian epiphyseal growth plate. In the present study, we report the identification of one of the clones as UDP-glucose pyrophosphorylase (UDPG-PPase) and propose a possible function for this enzyme in regulating hyaluronan (HA) synthesis in hypertrophic cartilage. We have cloned the 2.6 kb full-length cDNA for avian UDPG-PPase and confirmed its up-regulation in hypertrophic versus non-hypertrophic cartilage by Northern-blot analysis. The 6-fold increase in mRNA was paralleled by an equivalent increase in enzymic activity. The enzyme catalyses the conversion of glucose 1-phosphate into UDP-glucose, which is used to synthesize a number of cellular components, including HA. Overexpression of enzymically active UDPG-PPase in non-hypertrophic chondrocytes resulted in a 2-3-fold increase in total HA, as determined by a competitive binding assay and immunohistochemistry. In the developing growth plate, HA synthesis was elevated in the hypertrophic zone along with the up-regulation of the HA synthase (HAS)-2 gene. Our data suggest that an increase in both activities, UDPG-PPase and HAS-2, is required for non-hypertrophic chondrocytes to synthesize an amount of HA comparable with that in hypertrophic chondrocytes. Therefore we conclude that HA synthesis during chondrocyte differentiation is regulated at the level of the substrate-provider gene, UDPG-PPase, as well as the HAS genes.
机译:以前,我们已经进行了消减杂交,以鉴定在禽epi骨生长板的肥大软骨细胞中上调的基因。在本研究中,我们报告了一种克隆的鉴定为UDP-葡萄糖焦磷酸化酶(UDPG-PPase),并提出了该酶在调节肥大软骨中透明质酸(HA)合成中的可能功能。我们已经克隆了禽UDPG-PPase的2.6 kb全长cDNA,并通过Northern印迹分析证实了其在肥大性和非肥大性软骨中的上调。 mRNA的6倍增加与同等的酶活性增加平行。该酶催化将1-磷酸葡萄糖转化为UDP-葡萄糖,后者用于合成许多细胞成分,包括HA。通过竞争性结合测定和免疫组织化学测定,在非肥大性软骨细胞中酶活性UDPG-PPase的过表达导致总HA增加2-3倍。在发育中的生长板上,肥大区中的HA合成随着HA合酶(HAS)-2基因的上调而升高。我们的数据表明,非肥大性软骨细胞需要同时增加UDPG-PPase和HAS-2两种活性才能合成与肥大性软骨细胞相当的HA。因此,我们得出的结论是,软骨细胞分化过程中的HA合成受底物提供基因UDPG-PPase和HAS基因水平的调节。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号