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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Discrimination of micromass-induced chondrocytes from human mesenchymal stem cells by focal plane array-Fourier transform infrared microspectroscopy
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Discrimination of micromass-induced chondrocytes from human mesenchymal stem cells by focal plane array-Fourier transform infrared microspectroscopy

机译:焦平面阵列-傅里叶变换红外光谱法从人间充质干细胞中区分微质量诱导的软骨细胞

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摘要

Rapid and sensitive methods for identifying stem cell differentiation state are required for facilitating future stem cell therapies. We aimed to evaluate the capability of focal plane array-Fourier transform infrared (FPA-FTIR) microspectroscopy for characterising the differentiation of chondrocytes from human mesenchymal stem cells (hMSCs). Successful induction was validated by reverse transcription polymerase chain reaction (RT-PCR) and Western blot analysis for collagen and aggrecan expression as chondrocyte markers in parallel with the spectroscopy. Spectra derived from chondrocyte-induced cells revealed strong IR absorbance bands attributed to collagen near 1338 and 1234 cm~(-1) and proteoglycan at 1245 and 1175-960 cm~(-1) compared to the non-induced cells. In addition, spectra from control and induced cells are segregated into separate clusters in partial least squares discriminant analysis score plots at the very early stages of induction and discrimination of an independent set of validation spectra with 100% accuracy. The predominant bands responsible for this discrimination were associated with collagen and aggrecan protein concordant with those obtained from RT-PCR and Western blot techniques. Our findings support the capability of FPA-FTIR microspectroscopy as a label-free tool for stem cell characterization allowing rapid and sensitive detection of macromolecular changes during chondroenic differentiation.
机译:快速,灵敏的鉴定干细胞分化状态的方法是促进未来干细胞治疗所必需的。我们旨在评估焦平面阵列-傅立叶变换红外(FPA-FTIR)显微光谱技术表征人间充质干细胞(hMSCs)软骨细胞分化的能力。通过逆转录聚合酶链反应(RT-PCR)以及蛋白质和软骨聚集蛋白聚糖作为软骨细胞标记物的蛋白质印迹分析,Western blot分析与光谱学平行验证了成功的诱导。与未诱导的细胞相比,来自软骨细胞诱导的细胞的光谱显示出强的IR吸收带,归因于在1338和1234 cm〜(-1)附近的胶原和在1245和1175-960 cm〜(-1)的蛋白聚糖。此外,来自控制细胞和诱导细胞的光谱在诱导的最早期阶段以部分最小二乘判别分析得分图中的各个簇分离,并以100%的准确性区分独立的一组验证光谱。造成这种区别的主要条带与胶原蛋白和聚集蛋白聚糖蛋白相关,与从RT-PCR和Western blot技术获得的蛋白一致。我们的发现支持FPA-FTIR显微技术作为无标记工具进行干细胞表征的能力,从而可以在软骨分化过程中快速灵敏地检测大分子变化。

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