| Literature DB >> 31188523 |
Pengchao Zhang1,2, Xin Han1,2,3, Jun Yao4, Ning Shao1,2, Kai Zhang1,2, Yufu Zhou1,2, Youli Zu5, Bin Wang6, Lidong Qin1,2.
Abstract
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.Entities:
Keywords: RNA sequencing; analytical methods; cell protrusion; gene expression; microfluidics
Mesh:
Year: 2019 PMID: 31188523 PMCID: PMC7239316 DOI: 10.1002/anie.201903694
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336