首页> 外文期刊>Journal of Materials Chemistry, C. materials for optical and electronic devices >Monitoring in vitro neural stem cell differentiation based on surface-enhanced Raman spectroscopy using a gold nanostar array
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Monitoring in vitro neural stem cell differentiation based on surface-enhanced Raman spectroscopy using a gold nanostar array

机译:使用金纳米星阵列基于表面增强拉曼光谱监测体外神经干细胞分化

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The development of neurochips for non-invasive monitoring of neural stem cell stimulation is highly desirable and can enable the efficient optimization of tissue development protocols. Traditional methods, including cell staining and sorting, have long been used, but these techniques are time-consuming and may damage cells. Here, we have developed a cell-based chip to monitor the in vitro stepwise differentiation process of isolated mouse neural stem cells, the one-step differentiation of adult human neural stem cells (HB1.F3), and the electrochemical stimulation of rat pheochromocytoma PC12 cells. Results showed that each cell line exhibited a different behavior during differentiation. The DNA contents changed irregularly during the differentiation of HB1.F3 cells, while the percentage of proteins increased. In addition, the results revealed that the electrochemical stimulation of PC12 cells induced changes in the synthesis of DNA and proteins. The differentiation of isolated mouse neural stem cells showed a decrease in some peaks corresponding to the DNA content and an increase in the percentage of protein, in addition to the irregular behavior of some peaks related to both nucleic acids and proteins. The increase in protein percentage could indicate local variations in protein structure and a maturation shift. These results demonstrate that the SERS technique allows for more rapid biological sample analysis without time-consuming staining, enabling researchers to monitor engineered tissues and optimize culture conditions in a near real-time manner.
机译:非常需要开发用于无创监测神经干细胞刺激的神经芯片,并且可以有效优化组织发育方案。长期以来一直使用包括细胞染色和分选在内的传统方法,但是这些技术非常耗时,并且可能会损坏细胞。在这里,我们开发了一种基于细胞的芯片,用于监测离体小鼠神经干细胞的体外逐步分化过程,成年人类神经干细胞(HB1.F3)的一步分化以及大鼠嗜铬细胞瘤PC12的电化学刺激细胞。结果表明,每种细胞系在分化过程中表现出不同的行为。在HB1.F3细胞分化过程中,DNA含量无规律地变化,而蛋白质的百分比却增加了。另外,结果表明,PC12细胞的电化学刺激诱导了DNA和蛋白质合成的变化。分离的小鼠神经干细胞的分化显示出与DNA含量相对应的某些峰减少,蛋白质百分数增加,此外与核酸和蛋白质相关的某些峰的不规则行为。蛋白质百分比的增加可能表明蛋白质结构的局部变化和成熟度的变化。这些结果表明,SERS技术无需进行费时的染色即可进行更快速的生物样品分析,从而使研究人员能够以近乎实时的方式监测工程组织并优化培养条件。

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