| Literature DB >> 19074416 |
Dimitris G Placantonakis1, Mark J Tomishima, Fabien Lafaille, Sabrina C Desbordes, Fan Jia, Nicholas D Socci, Agnes Viale, Hyojin Lee, Neil Harrison, Viviane Tabar, Lorenz Studer.
Abstract
Human embryonic stem cells (hESCs) have enormous potential for applications in basic biology and regenerative medicine. However, harnessing the potential of hESCs toward generating homogeneous populations of specialized cells remains challenging. Here we describe a novel technology for the genetic identification of defined hESC-derived neural cell types using bacterial artificial chromosome (BAC) transgenesis. We generated hESC lines stably expressing Hes5::GFP, Dll1::GFP, and HB9::GFP BACs that yield green fluorescent protein (GFP)(+) neural stem cells, neuroblasts, and motor neurons, respectively. Faithful reporter expression was confirmed by cell fate analysis and appropriate transgene regulation. Prospective isolation of HB9::GFP(+) cells yielded purified human motor neurons with proper marker expression and electrophysiological activity. Global mRNA and microRNA analyses of Hes5::GFP(+) and HB9::GFP(+) populations revealed highly specific expression signatures, suggesting that BAC transgenesis will be a powerful tool for establishing expression libraries that define the human neural lineage and for accessing defined cell types in applications of human disease.Entities:
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Year: 2009 PMID: 19074416 DOI: 10.1634/stemcells.2008-0884
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277