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Identification of molecular markers for articular cartilage.

机译:鉴定关节软骨的分子标记。

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OBJECTIVE: The aim of the current study was to identify molecular markers for articular cartilage (AC) that can be used as tools for the quality control of tissue engineered (TE) cartilage. DESIGN: A genome-wide expression analysis was performed using RNA isolated from articular and growth plate (GP) cartilage, both extracted from the knee joints of 6 weeks old minipigs. After confirming the specific expression for selected genes by RT-PCR, these were used as molecular markers for the quality control of TE cartilage. RESULTS: Albeit several known chondrocyte markers were expressed to a similar extent in articular and GP cartilage, our genome-wide expression analysis led us to identify genes being selectively expressed in either GP or articular chondrocytes. These findings led us to perform a RT-PCR expression analysis for the corresponding genes to demonstrate the absence of GP-specific markers in TE cartilage, while common or AC markers were expressed. CONCLUSIONS: Taken together, these results provide important novel insights into chondrocyte biology in general and AC in particular. In addition, it is reasonable to speculate, that some of the identified genes play distinct roles in the regulation of articular chondrocyte differentiation and/or function, thereby raising the possibility that they may serve as targets for non-operative therapies of osteoarthritis (OA).
机译:目的:本研究的目的是鉴定关节软骨(AC)的分子标记物,这些分子标记物可用作组织工程(TE)软骨质量控制的工具。设计:使用从关节软骨和生长板(GP)软骨中分离的RNA进行全基因组表达分析,两者均从6周龄小猪的膝关节中提取。通过RT-PCR确认所选基因的特异性表达后,将这些用作TE软骨质量控制的分子标记。结果:尽管几种已知的软骨细胞标记物在关节软骨和GP软骨中表达的程度相似,但我们的全基因组表达分析使我们能够鉴定在GP或关节软骨细胞中选择性表达的基因。这些发现使我们对相应的基因进行了RT-PCR表达分析,以证明TE软骨中没有GP特异性标志物,而表达了普通或AC标志物。结论:总的来说,这些结果为一般的软骨细胞生物学尤其是AC提供了重要的新颖见解。此外,有理由推测,某些已鉴定的基因在调节关节软骨细胞分化和/或功能中起着不同的作用,从而增加了它们可能用作骨关节炎(OA)非手术治疗靶点的可能性。 。

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