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类固醇和胰岛素样生长因子I对解剖结构完整的小鼠关节软骨中大型蛋白聚糖合成的维持作用。

Maintenance of the synthesis of large proteoglycans in anatomically intact murine articular cartilage by steroids and insulin-like growth factor I.

作者信息

van der Kraan P M, Vitters E L, Postma N S, Verbunt J, van den Berg W B

机构信息

Department of Rheumatology, University Hospital, Nijmegen, The Netherlands.

出版信息

Ann Rheum Dis. 1993 Oct;52(10):734-41. doi: 10.1136/ard.52.10.734.

Abstract

OBJECTIVES

The exact regulation of the synthesis of cartilage specific molecules, such as collagen type II and aggrecan, by articular chondrocytes is unknown, but growth factors and hormones probably play an important part. The effects of glucocorticosteroids (prednisolone and triamcinolone), in combination with insulin-like growth factor I (IGF-I), on the synthesis and hydrodynamic volume of proteoglycans from murine patellar cartilage were investigated.

METHODS

The in vitro effect of IGF-I and steroids on proteoglycan synthesis in murine patellar cartilage was evaluated by [35S]sulphate incorporation in combination with dissociative gel chromatography using a Sephacryl S-1000 column. The impact of in vivo prednisolone (0-5 mg/kg) on proteoglycan synthesis in murine patellar cartilage was analysed by [35S]sulphate incorporation immediately after dissection from the knee joint.

RESULTS

Prednisolone stimulated proteoglycan synthesis in murine patellar cartilage from normal knees and in cartilage from knees injected with papain in vitro in the absence and presence of IGF-I. Moreover, oral administration of prednisolone for seven days to C57Bl10 mice resulted in enhanced proteoglycan synthesis in patellar cartilage. The incubation of patellar cartilage for 48 hours without serum or growth factors led to the synthesis of proteoglycans with a smaller hydrodynamic volume than those synthesised immediately after dissection of the patellae. This could either be circumvented by the addition of IGF-I or by the addition of glucocorticosteroids (prednisolone or triamcinolone) to the culture medium.

CONCLUSIONS

These results show that in a dose range of 0.0003-0.3 mmol/l, glucocorticosteroids, like IGF-I, stimulate proteoglycan synthesis and maintain the synthesis of hydrodynamically large proteoglycans by chondrocytes from murine articular cartilage. This indicates that glucocorticosteroids might play a part in the preservation of matrix integrity in articular cartilage.

摘要

目的

关节软骨细胞对软骨特异性分子(如Ⅱ型胶原蛋白和聚集蛋白聚糖)合成的确切调控机制尚不清楚,但生长因子和激素可能起着重要作用。本研究探讨了糖皮质激素(泼尼松龙和曲安奈德)与胰岛素样生长因子I(IGF-I)联合使用对小鼠髌软骨蛋白聚糖合成及流体动力学体积的影响。

方法

采用[35S]硫酸盐掺入法结合使用Sephacryl S-1000柱的解离凝胶色谱法,评估IGF-I和类固醇对小鼠髌软骨蛋白聚糖合成的体外作用。通过从膝关节解剖后立即进行[35S]硫酸盐掺入分析,研究体内泼尼松龙(0-5mg/kg)对小鼠髌软骨蛋白聚糖合成的影响。

结果

在无IGF-I和有IGF-I存在的情况下,泼尼松龙均能刺激正常膝关节小鼠髌软骨以及注射木瓜蛋白酶的膝关节软骨中的蛋白聚糖合成。此外,对C57Bl10小鼠口服泼尼松龙7天可增强髌软骨中的蛋白聚糖合成。髌软骨在无血清或生长因子的情况下孵育48小时,所合成的蛋白聚糖流体动力学体积比髌骨解剖后立即合成的蛋白聚糖小。添加IGF-I或向培养基中添加糖皮质激素(泼尼松龙或曲安奈德)均可避免这种情况。

结论

这些结果表明,在0.0003-0.3mmol/l的剂量范围内,糖皮质激素与IGF-I一样能刺激蛋白聚糖合成,并维持小鼠关节软骨细胞合成流体动力学体积大的蛋白聚糖。这表明糖皮质激素可能在维持关节软骨基质完整性方面发挥作用。

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