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首页> 外文期刊>Acta biomaterialia >Calcification of cartilage formed in vitro on calcium polyphosphate bone substitutes is regulated by inorganic polyphosphate.
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Calcification of cartilage formed in vitro on calcium polyphosphate bone substitutes is regulated by inorganic polyphosphate.

机译:无机多磷酸盐调节体外在多磷酸钙骨替代品上形成的软骨的钙化。

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摘要

A major challenge to the successful clinical application of bioengineered cartilage remains its integration to surrounding tissues upon implantation. One way to address this consists of generating biphasic constructs composed of articular cartilage formed in vitro on the top surface and integrated with the porous sub-surface of a bone substitute material - in the case of this study, calcium polyphosphate (CPP). To improve the mechanical integrity of the cartilage-bone substitute interface, attempts have been made to generate a zone of calcified cartilage (ZCC) within the CPP-cartilage interface, thereby mimicking the native joint architecture. The purpose of this work was to establish the effects of the degradation products of CPP on cartilage calcification in order to explain the observed positioning of a ZCC away from the interface junction. It was determined that polyphosphate released from the CPP accumulates within in vitro-grown cartilage and inhibits cartilage calcification in a concentration and chain length (i.e. molecular weight) dependent manner. It was found that this effect is transient as chondrocytes express exopolyphosphatases which hydrolyze polyphosphate to release orthophosphate. Hence, the generation of biphasic constructs with a properly located ZCC will require tailoring of CPP substrates with lower degradation rates or the upregulation of exopolyphosphatases by chondrocytes.
机译:生物工程软骨成功临床应用的主要挑战仍然是植入后其与周围组织的整合。解决此问题的一种方法是生成由关节软骨组成的双相结构,该关节软骨在体外形成于顶表面,并与骨替代材料的多孔子表面整合在一起(在本研究中为聚磷酸钙(CPP))。为了改善软骨-骨替代界面的机械完整性,已尝试在CPP-软骨界面内生成钙化软骨(ZCC)区域,从而模仿了天然的关节结构。这项工作的目的是确定CPP降解产物对软骨钙化的影响,以解释所观察到的ZCC远离界面交界处的位置。已确定从CPP释放的多磷酸盐在体外生长的软骨中积累,并以浓度和链长(即分子量)依赖性的方式抑制软骨钙化。发现该作用是瞬时的,因为软骨细胞表达胞外多磷酸酶,其水解多磷酸盐以释放正磷酸盐。因此,具有适当定位的ZCC的双相构建体的产生将需要定制CPP底物,使其具有较低的降解速率或软骨细胞对胞外多磷酸酶的上调。

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