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hOP-1、hTGF-β3 的协同诱导成骨作用和唑来膦酸在大孔珊瑚衍生羟磷灰石中的抑制作用。

Synergistic induction of bone formation by hOP-1, hTGF-beta3 and inhibition by zoledronate in macroporous coral-derived hydroxyapatites.

机构信息

Bone Research Unit, Medical Research Council/University of the Witwatersrand, Johannesburg, South Africa.

出版信息

Biomaterials. 2010 Sep;31(25):6400-10. doi: 10.1016/j.biomaterials.2010.04.037. Epub 2010 May 21.

Abstract

Thirty coral-derived calcium carbonate-based macroporous constructs with limited hydrothermal conversion to hydroxyapatite (7% HA/CC) were implanted in the rectus abdominis of three adult non-human primate Papio ursinus to investigate the intrinsic induction of bone formation. Macroporous constructs with 125 microg human recombinant osteogenic protein-1 (hOP-1) or 125 microg human recombinant transforming growth factor-beta(3) (hTGF-beta(3)) were also implanted. The potential synergistic interaction between morphogens was tested by implanting binary applications of hOP-1 and hTGF-beta(3) 5:1 by weight, respectively. To evaluate the role of osteoclastic activity on the implanted macroporous surfaces, coral-derived constructs were pre-loaded with 0.24 mg of bisphosphonate zoledronate (Zometa). To correlate the morphology of tissue induction with osteogenic gene expression and activation, harvested specimens on day 90 were analyzed for changes in OP-1 and TGF-beta(3) mRNA synthesis by quantitative real-time polymerase chain reaction (qRT-PCR). The induction of bone formation in 7% HA/CC solo correlated with OP-1 expression. Massive bone induction formed by binary applications of the recombinant morphogens. Single applications of hOP-1 and hTGF-beta(3) also resulted in substantial bone formation, not comparable however to synergistic binary applications. Zoledronate-treated macroporous constructs showed limited bone formation and in two specimens bone formation was altogether absent; qRT-PCR showed a prominent reduction of OP-1 gene expression whilst TGF-beta(3) expression was far greater than OP-1. The lack of bone formation by zoledronate-treated specimens indicates that osteoclastic activity on the implanted coral-derived constructs is critical for the spontaneous induction of bone formation. Indirectly, zoledronate-treated samples showing lack of OP-1 gene expression and absent or very limited bone formation by induction confirm that the spontaneous induction of bone formation by coral-derived macroporous constructs is initiated by secreted BMPs/OPs, in context the OP-1 isoform.

摘要

三十个珊瑚衍生的碳酸钙基大孔构建体,经过有限的水热转化为羟基磷灰石(7%HA/CC),被植入三只成年非人类灵长类动物狒狒的腹直肌中,以研究骨形成的内在诱导作用。还植入了 125μg 人重组骨形成蛋白-1(hOP-1)或 125μg 人重组转化生长因子-β3(hTGF-β3)的大孔构建体。通过分别以重量比 5:1 植入 hOP-1 和 hTGF-β3 的二元应用,测试了形态发生素之间的潜在协同相互作用。为了评估破骨细胞活性对植入大孔表面的作用,用 0.24mg 双膦酸盐唑来膦酸(Zometa)对珊瑚衍生的构建体进行预加载。为了将组织诱导的形态与成骨基因表达和激活相关联,对第 90 天收获的标本进行分析,通过定量实时聚合酶链反应(qRT-PCR)检测 OP-1 和 TGF-β3 mRNA 合成的变化。在 7%HA/CC 单一应用中,骨形成的诱导与 OP-1 表达相关。重组形态发生素的二元应用形成了大量的骨诱导。单一应用 hOP-1 和 hTGF-β3 也导致了大量的骨形成,但与协同的二元应用相比并不相当。唑来膦酸处理的大孔构建体显示出有限的骨形成,并且在两个标本中骨形成完全不存在;qRT-PCR 显示 OP-1 基因表达显著减少,而 TGF-β3 表达远高于 OP-1。唑来膦酸处理标本的骨形成缺失表明,植入珊瑚衍生的大孔构建体上的破骨细胞活性对于骨形成的自发诱导至关重要。间接地,唑来膦酸处理的样本显示缺乏 OP-1 基因表达,并且诱导的骨形成缺失或非常有限,这证实了珊瑚衍生的大孔构建体的自发诱导骨形成是由分泌的 BMPs/OPs 启动的,在这种情况下是 OP-1 同工型。

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