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首页> 外文期刊>Genesis: the journal of genetics and development >Biochemical, biophysical, and genetic changes of porcine trophoblast-derived stem-like cells during differentiation as evaluated using Raman microspectroscopy, Atomic force microscopy, and quantitative polymerase chain reaction
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Biochemical, biophysical, and genetic changes of porcine trophoblast-derived stem-like cells during differentiation as evaluated using Raman microspectroscopy, Atomic force microscopy, and quantitative polymerase chain reaction

机译:使用拉曼光谱,原子力显微镜和定量聚合酶链反应评估的猪滋养层来源干细胞样分化过程中的生化,生物物理和遗传变化

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Porcine trophoblast-derived stem-like cells grown into serum medium start to differentiate and become senescent within 30 days. However, trophoblast-derived cells, cultured in vitro in a defined and non-serum medium, have the regenerative properties, such as indefinite passage and foreign DNA receptivity, similar to stem cells. To evaluate the biochemical, biophysical, and genetic changes of the terminal differentiation of trophoblast derived cells, Raman microspectroscopy, atomic force microscopy, and qPCR were applied. It was found that Raman spectral intensities of characteristic peaks, cell morphology, and Young's modulus can be used to distinguish differentiated and undifferentiated trophoblast cells. In addition, 17 cytoskeleton and extracellular matrix-related genes were significantly impacted by medium type (non-serum versus serum). Our findings suggest that Raman microspectroscopy and atomic force microscopyboth considered as label-free, non-invasive techniquescan be applied to distinguish differentiated trophoblast cells, and cellular biochemical information and biophysical properties can be indicative of cellular differences during cell differentiation. In addition, most of cytoskeleton-related genes exhibit similar pattern to that of Young's modulus during trophoblast cell differentiation, indicating the potential connection between cytoskeleton-related genes and cellular stiffness. genesis 53:749-761, 2015. (c) 2015 Wiley Periodicals, Inc.
机译:生长在血清培养基中的猪滋养细胞来源的干样细胞在30天内开始分化并衰老。但是,在特定的非血清培养基中体外培养的滋养细胞来源的细胞具有与干细胞相似的再生特性,例如无限传代和外源DNA接受性。为了评估滋养细胞衍生细胞终末分化的生化,生物物理和遗传变化,应用了拉曼光谱,原子力显微镜和qPCR。发现特征峰的拉曼光谱强度,细胞形态和杨氏模量可用于区分分化和未分化的滋养层细胞。此外,培养基类型(非血清与血清)显着影响了17个细胞骨架和细胞外基质相关基因。我们的发现表明,拉曼光谱法和原子力显微镜均被视为无标签非侵入性技术,可用于区分分化的滋养细胞,细胞生化信息和生物物理特性可指示细胞分化过程中的细胞差异。此外,大多数与细胞骨架相关的基因在滋养层细胞分化过程中表现出与杨氏模量相似的模式,表明细胞骨架相关基因与细胞硬度之间存在潜在的联系。创刊53:749-761,2015.(c)2015 Wiley Periodicals,Inc.

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