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通过表面增强拉曼光谱对牙髓干细胞在细胞分化过程中的分子特征进行分析。

Molecular Profiling of Dental Pulp Stem Cells during Cell Differentiation by Surface Enhanced Raman Spectroscopy.

机构信息

Department of Endodontics, School and Hospital of Stomatology, Jilin University, Changchun 130021, Jilin P.R. China.

State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, Jilin P. R. China.

出版信息

Anal Chem. 2020 Mar 3;92(5):3735-3741. doi: 10.1021/acs.analchem.9b05026. Epub 2020 Feb 14.

Abstract

Dental pulp stem cells (DPSCs) are considered one of the key cells in tooth regeneration engineering. Understanding molecular biological information on DPSCs during differentiation is of great significance for the construction of tissue-engineered teeth. In this study, we investigated the differentiation process of DPSCs stimulated by drugs and gained molecular insights in the process. By using label-free and noninvasive surface enhanced Raman spectroscopy (SERS) to monitor molecular change profiling in the cell nucleus of single DPSCs during the differentiation process, we found that two pivotal differentiation biomarkers, alkaline phosphatase (ALP) and dentin sialophosphoprotein (DSPP), were overexpressed during the process. Continuous and intermittent monitoring of SERS spectra from the nuclear region indicated that the expression of proteins and related amino acids of tryptophan were markedly increased until peak period of differentiation (on day 14). Meanwhile corresponding transformation of DNA/RNA backbone vibrational modes was also observed during the differentiation process, indicating the occurrence of replication or transcription of DNA. The method provides a useful tool for the molecular biology studies of DPSCs differentiation, and the finding will broaden our understanding of DPSCs differentiation.

摘要

牙髓干细胞(DPSCs)被认为是牙齿再生工程中的关键细胞之一。了解 DPSCs 在分化过程中的分子生物学信息对于构建组织工程牙齿具有重要意义。在这项研究中,我们研究了药物刺激的 DPSCs 的分化过程,并在该过程中获得了分子见解。我们使用无标记和非侵入性的表面增强拉曼光谱(SERS)监测单个 DPSCs 细胞核中分子变化的轮廓,发现碱性磷酸酶(ALP)和牙本质涎磷蛋白(DSPP)这两个关键的分化生物标志物在分化过程中过度表达。从核区连续和间歇监测 SERS 光谱表明,色氨酸的蛋白质和相关氨基酸的表达在分化的高峰期(第 14 天)显著增加。同时,在分化过程中还观察到 DNA/RNA 骨架振动模式的相应转变,表明 DNA 的复制或转录发生。该方法为 DPSCs 分化的分子生物学研究提供了有用的工具,这一发现将拓宽我们对 DPSCs 分化的理解。

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