波形蛋白
免疫染色
间充质干细胞
信使核糖核酸
细胞生物学
荧光显微镜
伤口愈合
DNA
生物分子
分子生物学
化学
生物
荧光
材料科学
纳米技术
免疫组织化学
基因
免疫学
生物化学
物理
量子力学
作者
Patrick Vilela,Amelie Heuer‐Jungemann,Afaf H. El‐Sagheer,Tom Brown,Otto L. Muskens,Neil Smyth,Antonios G. Kanaras
出处
期刊:Small
[Wiley]
日期:2018-02-21
卷期号:14 (12): e1703489-e1703489
被引量:27
标识
DOI:10.1002/smll.201703489
摘要
Abstract Wound healing is a highly complex biological process, which is accompanied by changes in cell phenotype, variations in protein expression, and the production of active biomolecules. Currently, the detection of proteins in cells is done by immunostaining where the proteins in fixed cells are detected by labeled antibodies. However, immunostaining cannot provide information about dynamic processes in living cells, within the whole tissue. Here, an easy method is presented to detect the transition of epithelial to mesenchymal cells during wound healing. The method employs DNA‐coated gold nanoparticle fluorescent nanoprobes to sense the production of Vimentin mRNA expressed in mesenchymal cells. Fluorescence microscopy is used to achieve temporal detection of Vimentin mRNA in wounds. 3D light‐sheet microscopy is utilized to observe the dynamic expression of Vimentin mRNA spatially around the wounded site in skin tissue. The use of DNA–gold nanoprobes to detect mRNA expression during wound healing opens up new possibilities for the study of real‐time mechanisms in complex biological processes.
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