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高血糖状态通过刺激透明质酸合成调节人血管平滑肌细胞的结缔组织重构。

Hyperglycemic conditions modulate connective tissue reorganization by human vascular smooth muscle cells through stimulation of hyaluronan synthesis.

机构信息

Department of Medical Biochemistry and Genetics, University of Turku, FI-20520 Turku, Finland.

出版信息

Glycobiology. 2010 Sep;20(9):1117-26. doi: 10.1093/glycob/cwq076. Epub 2010 May 20.

DOI:10.1093/glycob/cwq076
PMID:20488939
Abstract

Changes in the extracellular matrix organization within vascular walls are critical events in the process of atherosclerosis including diabetic macroangiopathy. Here, we examined whether glucose can directly modulate connective tissue reorganization by human vascular smooth muscle cells (VSMCs). Using a collagen gel contraction (CGC) assay, we demonstrated that in comparison with normal glucose concentration (5 mM), high glucose concentration (25 mM) inhibits the efficacy of VSMCs to contract collagen gels. With human genome microarrays, we showed a significant increase in the expression of hyaluronan synthase 2 (HAS2) by VSMCs in hyperglycemic conditions. The finding was verified with quantitative real-time polymerase chain reaction, which also revealed that the expression of the other hyaluronan synthesizing enzymes, HAS1 and HAS3, was stimulated concomitantly. A corresponding increase was observed in hyaluronan (HA) production. Treatment of VSMCs either with hyaluronidase or with 4-methylumbelliferone, an inhibitor of HA synthesis, partially restored the diminished CGC efficacy of VSMCs in hyperglycemic conditions. In conclusion, high glucose concentration stimulated HA synthesis by VSMCs and modulated their ability to reorganize collagen-rich matrix. Because HA is known to enhance the development of atherosclerosis and restenosis after percutaneous coronary interventions, our study provides a new potential mechanism whereby hyperglycemia leads to disturbed vascular remodeling in diabetic patients through stimulation of HA synthesis.

摘要

血管壁细胞外基质组织的变化是动脉粥样硬化过程中的关键事件,包括糖尿病大血管病变。在这里,我们研究了葡萄糖是否可以直接调节人血管平滑肌细胞 (VSMC) 的结缔组织重构。通过胶原蛋白凝胶收缩 (CGC) 测定,我们证明与正常葡萄糖浓度 (5mM) 相比,高葡萄糖浓度 (25mM) 抑制了 VSMC 收缩胶原蛋白凝胶的效果。通过人类基因组微阵列,我们显示在高血糖条件下 VSMC 中透明质酸合酶 2 (HAS2) 的表达显著增加。定量实时聚合酶链反应也验证了这一发现,该反应还表明其他透明质酸合成酶 HAS1 和 HAS3 的表达也同时受到刺激。透明质酸 (HA) 的产生也相应增加。用透明质酸酶或 4-甲基伞形酮(HA 合成抑制剂)处理 VSMC,部分恢复了高血糖条件下 VSMC 收缩胶原蛋白丰富基质效果的降低。总之,高葡萄糖浓度刺激了 VSMC 中 HA 的合成,并调节了它们重塑富含胶原蛋白基质的能力。由于已知 HA 可增强经皮冠状动脉介入治疗后的动脉粥样硬化和再狭窄的发展,我们的研究提供了一个新的潜在机制,即通过刺激 HA 合成,高血糖导致糖尿病患者血管重构紊乱。

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