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肝素衍生寡糖对肝细胞生长因子产生的刺激作用。

Stimulation of hepatocyte growth factor production by heparin-derived oligosaccharides.

作者信息

Sakiyama Ryoichi, Fukuta Kazuhiro, Matsumoto Kunio, Furukawa Masumi, Takahashi Yoshihiro, Nakamura Toshikazu

机构信息

Division of Molecular Regenerative Medicine, Department of Biochemistry and Molecular Biology, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

出版信息

J Biochem. 2007 May;141(5):653-60. doi: 10.1093/jb/mvm067. Epub 2007 Feb 22.

DOI:10.1093/jb/mvm067
PMID:17317686
Abstract

We previously reported that heparin post-transcriptionally stimulates the production of hepatocyte growth factor (HGF). In this study, we addressed the size-dependency of heparin fragments on the HGF-inducing activity aiming to obtain fragments without antiblood coagulant activity. Heparin fragments, produced by digestion with heparinase, were size-fractionated and tested for HGF-inducing activity in cultured human fibroblasts. The HGF-inducing activity deceased with the reduction in oligosaccharide size. Decasaccharides exerted an activity comparable with undigested heparin, while smaller oligosaccharides showed lesser activities. The anticoagulant activity of heparin fragments also decreased with size and anticoagulant activity of decasaccharides was <13% that of undigested heparin. Further fractionation of decasaccharides by anion-exchange chromatography revealed that most of the decasaccharides had HGF-inducing activity and the extent of sulfation was roughly related to the activity. The lack of N-sulfation in heparin markedly reduced HGF-inducing activity, whereas 2-O-desulfation or 6-O-desulation had a lesser influence. Moreover, an N-sulfated disaccharide showed significant HGF-inducing activity, suggesting the involvement of N-sulfation in HGF-inducing activity. Because of the much reduced anticoagulant activity, potential applications of heparin-derived oligosaccharides such as decasaccharides is considerable as a therapeutic agent for many diseases.

摘要

我们之前报道过,肝素在转录后刺激肝细胞生长因子(HGF)的产生。在本研究中,我们探讨了肝素片段大小对HGF诱导活性的影响,旨在获得无抗凝血活性的片段。用肝素酶消化产生的肝素片段进行大小分级,并在培养的人成纤维细胞中测试其HGF诱导活性。HGF诱导活性随着寡糖大小的减小而降低。十糖表现出与未消化肝素相当的活性,而较小的寡糖活性较低。肝素片段的抗凝血活性也随大小而降低,十糖的抗凝血活性小于未消化肝素的13%。通过阴离子交换色谱对十糖进一步分级显示,大多数十糖具有HGF诱导活性,硫酸化程度与活性大致相关。肝素中N-硫酸化的缺失显著降低了HGF诱导活性,而2-O-去硫酸化或6-O-去硫酸化的影响较小。此外,一种N-硫酸化二糖表现出显著的HGF诱导活性,表明N-硫酸化参与了HGF诱导活性。由于抗凝血活性大大降低,肝素衍生的寡糖如十糖作为许多疾病的治疗剂具有相当大的潜在应用价值。

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