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Gold Nanoparticle-Based Surface-Enhanced Raman Scattering for Noninvasive Molecular Probing of Embryonic Stem Cell Differentiation

机译:基于金纳米粒子的表面增强拉曼散射用于胚胎干细胞分化的无创分子探测。

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This study reports the use of gold nanoparticle-based surface-enhanced Raman scattering (SERS) for probing the differentiation of mouse embryonic stem (mES) cells, including undifferentiated single cells, embryoid bodies (EBs), and terminally differentiated cardiomyocytes. Gold nanoparticles (GNPs) were successfully delivered into all 3 mES cell differentiation stages without affecting cell viability or proliferation. Transmission electron microscopy (TEM) confirmed the localization of GNPs inside the following cell organelles: mitochondria, secondary lysosome, and endoplasmic reticulum. Using bright- and dark-field imaging, the bright scattering of GNPs and nanoaggregates in all 3 ES cell differentiation stages could be visualized. EB (an early differentiation stage) and terminally differentiated cardiomyocytes both showed SERS peaks specific to metabolic activity in the mitochondria and to protein translation (amide I, amide II, and amide III peaks). These peaks have been rarely identified in undifferentiated single ES cells. Spatiotemporal changes observed in the SERS spectra from terminally differentiated cardiomyocyte tissues revealed local and dynamic molecular interactions as well as transformations during ES cell differentiation.
机译:这项研究报告了基于金纳米粒子的表面增强拉曼散射(SERS)用于探测小鼠胚胎干(mES)细胞的分化,包括未分化的单细胞,胚状体(EBs)和终末分化的心肌细胞。金纳米颗粒(GNP)已成功交付到所有3个mES细胞分化阶段,而不会影响细胞活力或增殖。透射电子显微镜(TEM)证实了GNP在以下细胞器内部的定位:线粒体,次级溶酶体和内质网。使用明场和暗场成像,可以观察到所有3个ES细胞分化阶段中GNP和纳米聚集体的明亮散射。 EB(早期分化阶段)和终末分化的心肌细胞均显示出针对线粒体代谢活性和蛋白质翻译的SERS峰(酰胺I,酰胺II和酰胺III峰)。在未分化的单个ES细胞中很少发现这些峰。从终末分化的心肌组织的SERS光谱中观察到的时空变化揭示了ES细胞分化过程中的局部和动态分子相互作用以及转化。

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