| Literature DB >> 18420830 |
Julia Ladewig1, Philipp Koch, Elmar Endl, Banu Meiners, Thoralf Opitz, Sebastien Couillard-Despres, Ludwig Aigner, Oliver Brüstle.
Abstract
A major prerequisite for the biomedical application of human embryonic stem cells (hESC) is the derivation of defined and homogeneous somatic cell types. Here we present a human doublecortin (DCX) promoter-based lineage-selection strategy for the generation of purified hESC-derived immature neurons. After transfection of hESC-derived neural precursors with a DCX-enhanced green fluorescent protein construct, fluorescence-activated cell sorting enables the enrichment of immature human neurons at purities of up to 95%. Selected neurons undergo functional maturation and are able to establish synaptic connections. Considering that the applicability of purified hESC-derived neurons would largely benefit from an efficient cryopreservation technique, we set out to devise defined freezing conditions involving caspase inhibition, which yield post-thaw recovery rates of up to 83%. Combined with our lineage-selection procedure this cryopreservation technique enables the generation of human neurons in a ready-to-use format for a large variety of biomedical applications.Entities:
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Year: 2008 PMID: 18420830 DOI: 10.1634/stemcells.2008-0007
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277