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首页> 外文期刊>Angewandte Chemie >High-Throughput Isolation of Cell Protrusions with Single-Cell Precision for Profiling Subcellular Gene Expression
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High-Throughput Isolation of Cell Protrusions with Single-Cell Precision for Profiling Subcellular Gene Expression

机译:具有单细胞精度的细胞突起的高通量分离,用于分析亚细胞基因表达

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摘要

Invading cancer cells extend cell protrusions, which guide cancer-cell migration and invasion, eventually leading to metastasis. The formation and activity of cell protrusions involve the localization of molecules and organelles at the cell front; however, it is challenging to precisely isolate these subcellular structures at the single-cell level for molecular analysis. Here, we describe a newly developed microfluidic platform capable of high-throughput isolation of cell protrusions at single-cell precision for profiling subcellular gene expression. Using this microfluidic platform, we demonstrate the efficient generation of uniform cell-protrusion arrays (more than 5000 cells with protrusions) for a series of cell types. We show precise isolation of cell protrusions with high purity at single-cell precision for subsequent RNA-Seq analysis, which was further validated by RT-qPCR and RNA FISH. Our highly controlled protrusion isolation method opens a new avenue for the study of subcellular functional mechanisms and signaling pathways in metastasis.
机译:入侵癌细胞延长细胞突起,引导癌细胞迁移和侵袭,最终导致转移。细胞突起的形成和活性涉及在细胞前部的分子和细胞器的定位;然而,精确地将这些亚细胞结构精确分离在单细胞水平以进行分子分析。在这里,我们描述了一种新开发的微流体平台,能够以单细胞精度为细胞突起的高通量隔离,以进行分析亚细胞基因表达。使用该微流体平台,我们证明了一系列细胞类型的高效产生均匀的细胞 - 突起阵列(具有突起的5000多个细胞)。对于随后的RNA-SEQ分析,我们表现出具有高纯度的细胞突起的精确隔离,用于随后的RNA-SEQ分析,通过RT-QPCR和RNA鱼进一步验证。我们的高度控制突出隔离方法为转移中的亚细胞功能机制和信号通路进行了新的途径。

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