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High-Throughput Isolation of Cell Protrusions with Single-Cell Precision for Profiling Subcellular Gene Expression.
Zhang, Pengchao; Han, Xin; Yao, Jun; Shao, Ning; Zhang, Kai; Zhou, Yufu; Zu, Youli; Wang, Bin; Qin, Lidong.
Afiliação
  • Zhang P; Department of Nanomedicine, Houston Methodist Research Institute, Houston, TX, 77030, USA.
  • Han X; Department of Cell and Developmental Biology, Weill Medical College of Cornell University, New York, NY, 10065, USA.
  • Yao J; Department of Nanomedicine, Houston Methodist Research Institute, Houston, TX, 77030, USA.
  • Shao N; Department of Cell and Developmental Biology, Weill Medical College of Cornell University, New York, NY, 10065, USA.
  • Zhang K; Present address: School of Medicine and Life Sciences, Nanjing University of Chinese Medicine, Nanjing, 210023, P. R. China.
  • Zhou Y; Department of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
  • Zu Y; Department of Nanomedicine, Houston Methodist Research Institute, Houston, TX, 77030, USA.
  • Wang B; Department of Cell and Developmental Biology, Weill Medical College of Cornell University, New York, NY, 10065, USA.
  • Qin L; Department of Nanomedicine, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Angew Chem Int Ed Engl ; 58(39): 13700-13705, 2019 09 23.
Article em En | MEDLINE | ID: mdl-31188523
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Perfilação da Expressão Gênica / Microfluídica / Ensaios de Triagem em Larga Escala / Análise de Célula Única Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Perfilação da Expressão Gênica / Microfluídica / Ensaios de Triagem em Larga Escala / Análise de Célula Única Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article