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Glial Fibrillary Acidic Protein as Biomarker Indicates Purity and Property of Auricular Chondrocytes

机译:胶质纤维酸性蛋白质作为生物标志物表明耳廓软骨细胞的纯度和性质

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Instead of the silicone implants previously used for repair and reconstruction of the auricle and nose lost due to accidents and disease, a new treatment method using tissue-engineered cartilage has been attracting attention. The quality of cultured cells is important in this method because it affects treatment outcomes. However, a marker of chondrocytes, particularly auricular chondrocytes, has not yet been established. The objective of this study was to establish an optimal marker to evaluate the quality of cultured auricular chondrocytes as a cell source of regenerative cartilage tissue. Gene expression levels were comprehensively compared using the microarray method between human undifferentiated and dedifferentiated auricular chondrocytes to investigate a candidate quality control index with an expression level that is high in differentiated cells, but markedly decreases in dedifferentiated cells. We identified glial fibrillary acidic protein (GFAP) as a marker that decreased with serial passages in auricular chondrocytes. GFAP was not detected in articular chondrocytes, costal chondrocytes, or fibroblasts, which need to be distinguished from auricular chondrocytes in cell cultures. GFAP mRNA expression was observed in cultured auricular chondrocytes, and GFAP protein levels were also measured in the cell lysates and culture supernatants of these cells. However, GFAP levels detected from mRNA and protein in cell lysates were significantly decreased by increases in the incubation period. In contrast, the amount of protein in the cell supernatant was not affected by the incubation period. Furthermore, the protein level of GFAP in the supernatants of cultured cells correlated with the in vitro and in vivo production of the cartilage matrix by these cells. The productivity of the cartilage matrix in cultured auricular chondrocytes may be predicted by measuring GFAP protein levels in the culture supernatants of these cells. Thus, GFAP is regarded as a marker of the purity and properties of cultured auricular chondrocytes.
机译:代替以前用于修复和重建的硅氧烷植入物,由于事故和疾病导致耳廓和鼻子丢失,使用组织工程化软骨的新治疗方法一直引起注意。在这种方法中,培养细胞的质量很重要,因为它会影响治疗结果。然而,尚未建立软骨细胞,特别是耳廓的软骨细胞的标记。本研究的目的是建立最佳标记,以评估培养的耳廓软骨细胞的质量作为再生软骨组织的细胞来源。使用人未分化的和去除了的耳廓软骨细胞之间的微阵列方法进行全面地进行基因表达水平,以研究候选质量控制指数,其表达水平高在于分化细胞,但在去细胞的细胞中显着降低。我们将胶质纤维酸性蛋白(GFAP)鉴定为用耳廓软骨细胞的串行通道降低的标记。在关节软骨细胞,昂贵的软骨细胞或成纤维细胞中未检测到GFAP,其需要与细胞培养物中的耳廓软骨细胞区分开。在培养的耳廓软骨细胞中观察到GFAP mRNA表达,并且在细胞裂解物和这些细胞的培养上清液中也测量GFAP蛋白水平。然而,通过孵育期的增加,从细胞裂解物中检测到的mRNA和蛋白质中检测到的GFAP水平显着降低。相反,细胞上清液中的蛋白质的量不受培养期的影响。此外,培养细胞上清液中的GFAP的蛋白质水平与这些细胞的体外和体内生产的软骨基质相关。通过测量这些细胞的培养上清液中的GFAP蛋白水平,可以预测软骨基质在培养的耳廓内软骨细胞中的生产率。因此,GFAP被认为是培养的耳廓软骨细胞的纯度和性质的标志物。

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