Takeda Yuji S, Xu Qiaobing
Department of Biomedical Engineering, Tufts University, Medford, MA, United States of America.
PLoS One. 2015 Aug 6;10(8):e0135111. doi: 10.1371/journal.pone.0135111. eCollection 2015.
Exosomes deliver functional proteins and genetic materials to neighboring cells, and have potential applications for tissue regeneration. One possible mechanism of exosome-promoted tissue regeneration is through the delivery of microRNA (miRNA). In this study, we hypothesized that exosomes derived from neuronal progenitor cells contain miRNAs that promote neuronal differentiation. We treated mesenchymal stem cells (MSCs) daily with exosomes derived from PC12 cells, a neuronal cell line, for 1 week. After the treatment with PC12-derived exosomes, MSCs developed neuron-like morphology, and gene and protein expressions of neuronal markers were upregulated. Microarray analysis showed that the expression of miR-125b, which is known to play a role in neuronal differentiation of stem cells, was much higher in PC12-derived exosomes than in exosomes from B16-F10 melanoma cells. These results suggest that the delivery of miRNAs contained in PC12-derived exosomes is a possible mechanism explaining the neuronal differentiation of MSC.
外泌体将功能性蛋白质和遗传物质传递给邻近细胞,并在组织再生方面具有潜在应用。外泌体促进组织再生的一种可能机制是通过传递微小RNA(miRNA)。在本研究中,我们假设源自神经祖细胞的外泌体含有促进神经元分化的miRNA。我们每天用源自神经细胞系PC12细胞的外泌体处理间充质干细胞(MSC),持续1周。用源自PC12细胞的外泌体处理后,MSC呈现出神经元样形态,并且神经元标志物的基因和蛋白表达上调。微阵列分析表明,已知在干细胞神经元分化中起作用的miR-125b在源自PC12细胞的外泌体中的表达远高于源自B16-F10黑色素瘤细胞的外泌体。这些结果表明,源自PC12细胞的外泌体中所含miRNA的传递是解释MSC神经元分化的一种可能机制。