[骨形态发生蛋白-12 (BMP-12)转基因诱导骨缺损组织再生]。

Nobuhiro Goto
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引用次数: 1

摘要

除BMP-2、bmp - 4和bmp - 7外,已知BMP-12可诱导肌腱/韧带样组织的形成。然而,蛋白质在骨或软骨愈合过程中的作用尚未得到充分研究。本研究的目的是研究编码BMP-12的质粒载体是否会诱导大鼠骨缺损模型的肌腱/韧带形成。将含有100 μ g编码BMP-12或BMP-2的质粒载体的冻干间胶原颗粒植入大鼠股骨干骺端骨缺损。于术后2周、4周和8周取标本,进行组织学和实时PCR分析。BMP-12转基因在2周时显示明显的纤维形成。因此,在8周时用骨代替组织。BMP-12基因转染2周后,III型胶原基因表达上调,4周后,弹性蛋白和Six1基因表达上调。这些与肌腱/韧带形成密切相关的基因在8周后为成骨做准备时表达减少。另一方面,BMP-2转基因可快速诱导I型胶原、ALP等骨相关基因的合成。由此可见,BMP-12可以促进大鼠骨缺损早期愈合阶段肌腱/韧带样组织的发育。在骨上维持这种组织的生成可能有助于改进牙周组织工程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Tissue regeneration induced by a transgene for bone morphogenetic protein-12 (BMP-12) in a bone defect].

BMP-12, other than BMP-2, 4, and 7, is known to induce the formation of tendon/ligament-like tissues. However, the role of the protein in the process of bone or cartilage healing has not been adequately examined. The purpose of the present study was to examine if a plasmid vector encoding BMP-12 would induce tendon/ ligament formation in a rat bone defect model. A lyophilized atelocollagen pellet with 100 microg of a plasmid vector encoding BMP-12 or BMP-2 was implanted in a bone defect of a rat femoral metaphysis. The samples were retrieved at 2, 4 and 8 weeks post-operation and subjected to histology and real-time PCR analysis. BMP-12 transgene indicated prominent fibrogenesis at 2 weeks. Consequently, the tissue was substituted by bone at 8 weeks. The gene expression of collagen type III was up-regulated by BMP-12 gene transfer after 2 weeks, followed by an increase of elastin and Six1 genes after 4 weeks. These genes, which are intimately related to tendon/ligament formation, decreased in expression at 8 weeks in preparation for osteogenesis afterward. On the other hand, the BMP-2 transgene quickly induced the synthesis of bone-related genes such as collagen type I and ALP. It is concluded that BMP-12 can initiate the development of tendon/ligament-like tissue in a rat bone defect at early healing stages. Maintaining such generation of tissue on bone could be useful for modifying periodontal tissue engineering.

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