Cancer Cell Membrane Vesicle for Multiplex MicroRNA Imaging in Living Cells.
Huiting LuKeke GuoYu CaoFan YangDongdong WangLei DouYayun LiuHaifeng DongPublished in: Analytical chemistry (2020)
Highly efficient cellular transfection and intracellular signal amplification is a prerequisite for low-abundant microRNA (miRNA) imaging and biomedical application. Herein, we report a functional cancer cell membrane (CM) vesicle, Au-P/DSN@CM (DSN, double-specific nucleases), which consists of Au nanoparticles modified with three types of fluorescent miRNA detection probes (Au-P) and DSN that simultaneously encapsulate in cancer CM. We find that the Au-P/DSN@CM could specifically target the cancer cell and transfect the cell with higher efficiency than Au nanoparticles. The internalized Au-P/DSN@CM could further specifically recognize the target miRNA and induce DSN-assisted target recycle signal amplification, leading to multiple miRNA simultaneous detection with high sensitivity. It successfully detects oncogenic miRNAs in MCF-7 cells with high sensitivity and is amenable to monitor the dynamic expression change of oncogenic miRNAs in cancer cells. Our study represents a promising gene delivery vector for cancer diagnosis and potential therapy.
Keyphrases
- papillary thyroid
- living cells
- sensitive detection
- highly efficient
- squamous cell
- reduced graphene oxide
- high resolution
- label free
- transcription factor
- squamous cell carcinoma
- single molecule
- induced apoptosis
- small molecule
- stem cells
- loop mediated isothermal amplification
- nucleic acid
- mesenchymal stem cells
- real time pcr
- fluorescence imaging
- high throughput
- cell death
- reactive oxygen species
- cell cycle arrest