氨基葡萄糖可降低人骨关节炎软骨外植体中合成代谢和分解代谢基因的表达。

Glucosamine decreases expression of anabolic and catabolic genes in human osteoarthritic cartilage explants.

作者信息

Uitterlinden E J, Jahr H, Koevoet J L M, Jenniskens Y M, Bierma-Zeinstra S M A, Degroot J, Verhaar J A N, Weinans H, van Osch G J V M

机构信息

Erasmus MC, University Medical Center Rotterdam, Department of Orthopaedics, The Netherlands.

出版信息

Osteoarthritis Cartilage. 2006 Mar;14(3):250-7. doi: 10.1016/j.joca.2005.10.001. Epub 2005 Nov 18.

Abstract

OBJECTIVE

To investigate the effect of glucosamine (GlcN) in a human osteoarthritic explant model on expression of genes involved in anabolic and catabolic activities of chondrocytes.

METHODS

Human osteoarthritic explants, obtained during knee arthroplasty surgery, were pre-cultured (3 days) and treated with glucosamine-hydrochloride (GlcN-HCl) or glucosamine-3-sulphate (GlcN-S) at 0.5mM and 5mM (4 days). RNA was isolated from the explants and real time RT-PCR was performed. Additionally, total matrix metalloproteinase (MMP) activity was measured in culture medium.

RESULTS

Addition of 5mM GlcN led to significant down-regulation of aggrecan (2.65-7.73-fold) and collagen type II (7.75-22.17-fold) gene expression, indicating inhibited anabolic activity. Considering catabolic activities, 5mM GlcN significantly down-regulated aggrecanase-1 and MMP3 and 5mM GlcN-S additionally down-regulated aggrecanase-2 and tissue inhibitor of MMP gene expression significantly. Gene expression was not significantly altered by 0.5mM GlcN. Total MMP activity in culture medium was only significantly reduced after addition of 5mM GlcN-HCl.

CONCLUSION

The effects of GlcN on gene expression in a human osteoarthritic explant model suggest that enzymatic breakdown of the extra-cellular matrix might be reduced by the addition of 5mM GlcN. Additionally, restoration of already damaged cartilage is not to be expected, because gene expression of anabolic genes is also down-regulated. We suggest that chondroprotective properties of GlcN in vivo may be based on inhibiting further degradation due to catabolic activities, rather than on the ability to rebuild cartilage.

摘要

目的

研究氨基葡萄糖(GlcN)在人骨关节炎外植体模型中对软骨细胞合成代谢和分解代谢相关基因表达的影响。

方法

在膝关节置换手术中获取人骨关节炎外植体,先预培养(3天),然后用0.5mM和5mM的盐酸氨基葡萄糖(GlcN-HCl)或硫酸氨基葡萄糖(GlcN-S)处理(4天)。从外植体中提取RNA并进行实时逆转录聚合酶链反应。此外,在培养基中测量总基质金属蛋白酶(MMP)活性。

结果

添加5mM GlcN导致聚集蛋白聚糖(2.65 - 7.73倍)和Ⅱ型胶原(7.75 - 22.17倍)基因表达显著下调,表明合成代谢活性受到抑制。考虑分解代谢活性,5mM GlcN显著下调聚集蛋白聚糖酶-1和MMP3,5mM GlcN-S还显著下调聚集蛋白聚糖酶-2和MMP组织抑制剂基因表达。0.5mM GlcN对基因表达无显著影响。仅在添加5mM GlcN-HCl后,培养基中的总MMP活性才显著降低。

结论

GlcN在人骨关节炎外植体模型中对基因表达的影响表明,添加5mM GlcN可能会减少细胞外基质的酶促降解。此外,由于合成代谢基因的表达也下调,因此不能期望恢复已受损的软骨。我们认为,GlcN在体内的软骨保护特性可能基于抑制分解代谢活动导致的进一步降解,而非重建软骨的能力。

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