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热等离子体调控线粒体代谢状态促进牙髓干细胞定向分化。

Thermoplasmonic Regulation of the Mitochondrial Metabolic State for Promoting Directed Differentiation of Dental Pulp Stem Cells.

机构信息

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

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

出版信息

Anal Chem. 2022 Jul 12;94(27):9564-9571. doi: 10.1021/acs.analchem.2c00288. Epub 2022 Jun 28.

Abstract

Regulating stem cell differentiation in a controllable way is significant for regeneration of tissues. Herein, we report a simple and highly efficient method for accelerating the stem cell differentiation of dental pulp stem cells (DPSCs) based on the synergy of the electromagnetic field and the photothermal (thermoplasmonic) effect of plasmonic nanoparticles. By simple laser irradiation at 50 mW/cm (10 min per day, totally for 5 days), the thermoplasmonic effect of Au nanoparticles (AuNPs) can effectively regulate mitochondrial metabolism to induce the increase of mitochondrial membrane potential and further drive energy increase during the DPSC differentiation process. The proposed method can specifically regulate DPSCs' cell differentiation toward odontoblasts, with the differentiation time reduced to only 5 days. Simultaneously, the molecular profiling change of mitochondria within DPSCs during the cell differentiation process is revealed by in situ surface-enhanced Raman spectroscopy. It clearly demonstrates that the expression of hydroxyproline and glutamate gradually increases with prolonging of the differentiation days. The developed method is simple, robust, and rapid for stem cell differentiation of DPSCs, which would be beneficial to tissue engineering and regenerative medicine.

摘要

以可控的方式调控干细胞分化对于组织再生具有重要意义。在此,我们报告了一种基于电磁场协同和等离子体纳米粒子光热(热等离子体)效应的简单而高效的方法,用于加速牙髓干细胞(DPSCs)的干细胞分化。通过简单的激光辐照(50 mW/cm,每天 10 分钟,总共 5 天),金纳米粒子(AuNPs)的热等离子体效应可以有效调节线粒体代谢,诱导线粒体膜电位增加,并进一步在 DPSCs 分化过程中驱动能量增加。所提出的方法可以特异性地调节 DPSCs 向成牙本质细胞的分化,将分化时间缩短至仅 5 天。同时,通过原位表面增强拉曼光谱揭示了 DPSCs 细胞分化过程中线粒体内部的分子特征变化。结果清楚地表明,随着分化天数的延长,羟基脯氨酸和谷氨酸的表达逐渐增加。所开发的方法简单、稳健、快速,可用于 DPSCs 的干细胞分化,这将有利于组织工程和再生医学。

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