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大鼠激素性骨坏死股骨头中 Runx2、Osterix 和 AJ18 的动态表达。

Dynamic expression of Runx2, Osterix and AJ18 in the femoral head of steroid-induced osteonecrosis in rats.

机构信息

Tianjin Hospital Department of Orthopaedics, Tianjin Medical University General Hospital, Tianjin, China.

出版信息

Orthop Surg. 2010 Nov;2(4):278-84. doi: 10.1111/j.1757-7861.2010.00100.x.

Abstract

OBJECTIVE

To study dynamic changes in gene expression and protein synthesis of runt-related transcription factor-2 (Runx2), Osterix and AJ18 in the femoral head of steroid-induced osteonecrosis in rats.

METHODS

Forty mature Wistar rats, 250-270 g (mean, 260 g) in weight, were randomly divided into model (30 rats) and control groups (10 rats). An early rat model of femoral head necrosis (FHN) was created by weekly injections of dexamethasone (20 mg/kg) into alternate sides of the gluteus maximus and twice-weekly training on a laboratory animal treadmill for 8 weeks. Hematoxylin and eosin (HE) staining was used to determine whether osteonecrosis had been successfully induced, and the model was then divided into equal 8, 10 and 12 week groups. At the end of the appropriate time period, total RNA and total protein were extracted from the femoral heads, and then real-time quantitative polymerase chain reaction and Western blot were performed to detect dynamic changes in the expression of Runx2, Osterix and AJ18 and protein synthesis in femoral heads with steroid-induced osteonecrosis in rats.

RESULTS

At the post-modeling eighth, tenth and twelfth week, expression of Runx2 mRNA, Osterix mRNA and related protein synthesis were significantly down-regulated compared to that of the control group, which showed a downward trend with time; while expression of AJ18 mRNA and protein synthesis in the model group was much higher than in the control group, which showed an upward trend with time.

CONCLUSION

Glucocorticoids may induce femoral head osteonecrosis by down-regulating Runx2/Osterix mRNA and up-regulating AJ18 mRNA.

摘要

目的

研究 Runt 相关转录因子 2(Runx2)、成骨相关转录因子 2(Osterix)和 A 框锌指蛋白 18(AJ18)在大鼠激素性股骨头坏死模型中的基因表达和蛋白合成的动态变化。

方法

40 只成熟 Wistar 大鼠,体重 250-270 g(平均 260 g),随机分为模型组(30 只)和对照组(10 只)。每周向大鼠臀肌两侧注射地塞米松(20 mg/kg),并在实验室动物跑步机上进行双周训练 8 周,建立大鼠早期股骨头坏死(FHN)模型。苏木精和伊红(HE)染色法确定是否成功诱导了骨坏死,然后将模型分为 8、10 和 12 周组,每组 10 只。在适当的时间段结束时,从股骨头中提取总 RNA 和总蛋白,然后进行实时定量聚合酶链反应和 Western blot 检测,以检测大鼠激素性股骨头坏死模型中 Runx2、Osterix 和 AJ18 的表达和蛋白合成的动态变化。

结果

在造模后第 8、10 和 12 周,与对照组相比,Runx2mRNA、OsterixmRNA 及其相关蛋白的表达均明显下调,且随时间呈下降趋势;而模型组 AJ18mRNA 和蛋白的表达均明显高于对照组,且随时间呈上升趋势。

结论

糖皮质激素可能通过下调 Runx2/OsterixmRNA 并上调 AJ18mRNA 诱导股骨头坏死。

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