...
首页> 外文期刊>Histochemistry and cell biology >Morphological, genetic and phenotypic comparison between human articular chondrocytes and cultured chondrocytes
【24h】

Morphological, genetic and phenotypic comparison between human articular chondrocytes and cultured chondrocytes

机译:人关节软骨细胞和培养的软骨细胞的形态,遗传和表型比较

获取原文
获取原文并翻译 | 示例

摘要

Articular cartilage is an avascular and aneural tissue with limited capacity for regeneration. On large articular lesions, it is recommended to use regenerative medicine strategies, like autologous chondrocyte implantation. There is a concern about morphological changes that chondrocytes suffer once they have been isolated and cultured. Due to the fact that there is little evidence that compares articular cartilage chondrocytes with cultured chondrocytes, in this research we proposed to obtain chondrocytes from human articular cartilage, compare them with themselves once they have been cultured and characterize them through genetic, phenotypic and morphological analysis. Knee articular cartilage samples of 10 mm were obtained, and each sample was divided into two fragments; a portion was used to determine gene expression, and from the other portion, chondrocytes were obtained by enzymatic disaggregation, in order to be cultured and expanded in vitro. Subsequently, morphological, genetic and phenotypic characteristics were compared between in situ (articular cartilage) and cultured chondrocytes. Obtained cultured chondrocytes were rounded in shape, possessing a large nucleus with condensed chromatin and a clear cytoplasm; histological appearance was quite similar to typical chondrocyte. The expression levels of COL2A1 and COL10A1 genes were higher in cultured chondrocytes than in situ chondrocytes; moreover, the expression of COL1A1 was almost undetectable on cultured chondrocytes; likewise, COL2 and SOX9 proteins were detected by immunofluorescence. We concluded that chondrocytes derived from adult human cartilage cultured for 21 days do not tend to dedifferentiate, maintaining their capacity to produce matrix and also retaining their synthesis capacity and morphology.
机译:关节软骨是再生能力有限的无血管和无神经的组织。对于大的关节病变,建议使用再生医学策略,例如自体软骨细胞植入。软骨细胞一旦被分离和培养就会遭受形态变化的困扰。由于几乎没有证据可以将关节软骨软骨细胞与培养的软骨细胞进行比较,因此在这项研究中,我们建议从人关节软骨中获取软骨细胞,将其与自身软骨进行培养后进行比较,并通过遗传,表型和形态分析对其进行表征。获得了10mm的膝关节软骨样品,并且将每个样品分成两个片段。一部分用于确定基因表达,另一部分通过酶促分解获得软骨细胞,以便在体外培养和扩增。随后,比较了原位(关节软骨)和培养的软骨细胞的形态,遗传和表型特征。获得的培养的软骨细胞呈圆形,具有大核,浓缩的染色质和透明的细胞质。组织学外观与典型的软骨细胞非常相似。培养的软骨细胞中COL2A1和COL10A1基因的表达水平高于原位软骨细胞。此外,在培养的软骨细胞上几乎检测不到COL1A1的表达。同样,通过免疫荧光检测COL2和SOX9蛋白。我们得出的结论是,培养了21天的成年人类软骨软骨细胞不会趋于去分化,保持了它们产生基质的能力,并且还保留了它们的合成能力和形态。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号