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骨形态发生蛋白与Smad在羊肌腱-骨愈合中的表达

Bone morphogenetic proteins and Smad expression in ovine tendon-bone healing.

作者信息

Yu Yan, Bliss James P, Bruce Warrick J M, Walsh William R

机构信息

Surgical & Orthopaedic Research Laboratories, Prince of Wales Clinical School, University of New South Wales, Sydney, New South Wales, Australia.

出版信息

Arthroscopy. 2007 Feb;23(2):205-10. doi: 10.1016/j.arthro.2006.08.023.

Abstract

PURPOSE

Bone morphogenetic proteins (BMPs) are being developed to improve tendon-bone healing. To do this, it is essential to understand the endogenous expression of BMPs and their downstream signal transduction factors, Smads, during tendon-bone healing.

METHODS

An extra-articular patellar tendon-bone healing ovine model was set up, and histologic evaluation of the healing progress at the tendon-bone interface at 1, 2, 3, and 6 weeks was performed. Immunohistochemical staining of BMP-2, BMP-7, Smad1, Smad4, and Smad5 was carried out in all sections.

RESULTS

The model revealed formation of a loose granuloma tissue layer between the tendon and bone at 1 week, remodeling starting at 2 weeks, and Sharpey-like collagen fiber formation at 3 and 6 weeks. All detected factors were elevated at the tendon-bone interface during healing, and the expression peaked at 2 to 3 weeks. The cells involved were osteoblastic-like cells, osteoclastic-like cells, mesenchymal cells, and fibroblasts. BMP-7 staining was mainly at the interface close to the bony side, whereas BMP-2 expression shifted to the tendon side at 6 weeks. The expression pattern of Smad1 and Smad5 was similar to that of BMP-7. Smad1 was also found to be expressed in osteoclastic-like cells at 1 and 2 weeks. Smad4 expression was the highest among all of the factors at all time points.

CONCLUSIONS

The data suggest that endogenous BMP-2 and BMP-7 participate in tendon-bone healing and their functions involve their downstream signal transduction mediators, Smad1, Smad4, and Smad5.

CLINICAL RELEVANCE

The temporal expression of BMPs should be considered when setting up therapeutic strategies using BMPs.

摘要

目的

骨形态发生蛋白(BMPs)正被研发用于改善肌腱-骨愈合。为此,了解BMPs及其下游信号转导因子Smads在肌腱-骨愈合过程中的内源性表达至关重要。

方法

建立关节外髌腱-骨愈合绵羊模型,并在第1、2、3和6周对肌腱-骨界面的愈合进程进行组织学评估。对所有切片进行BMP-2、BMP-7、Smad1、Smad4和Smad5的免疫组织化学染色。

结果

该模型显示,在第1周时肌腱与骨之间形成疏松的肉芽肿组织层,2周时开始重塑,3周和6周时出现类Sharpey胶原纤维形成。在愈合过程中,所有检测因子在肌腱-骨界面均升高,且表达在2至3周达到峰值。涉及的细胞有成骨样细胞、破骨样细胞、间充质细胞和成纤维细胞。BMP-7染色主要位于靠近骨侧的界面,而BMP-2在6周时表达转移至肌腱侧。Smad1和Smad5的表达模式与BMP-7相似。在第1周和第2周时,还发现Smad1在破骨样细胞中表达。在所有时间点,Smad4的表达在所有因子中最高。

结论

数据表明内源性BMP-2和BMP-7参与肌腱-骨愈合,其功能涉及其下游信号转导介质Smad1、Smad4和Smad5。

临床意义

在制定使用BMPs的治疗策略时,应考虑BMPs的时间表达。

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