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Cell-Surface Proteomics Identifies Lineage-Specific Markers of Embryo-Derived Stem Cells

The advent of reprogramming and its impact on stem cell biology has renewed interest in lineage restriction in mammalian embryos, the source of embryonic (ES), epiblast (EpiSC), trophoblast (TS), and extraembryonic endoderm (XEN) stem cell lineages. Isolation of specific cell types during stem cell...

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Detalles Bibliográficos
Autores principales: Rugg-Gunn, Peter J., Cox, Brian J., Lanner, Fredrik, Sharma, Parveen, Ignatchenko, Vladimir, McDonald, Angela C.H., Garner, Jodi, Gramolini, Anthony O., Rossant, Janet, Kislinger, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405530/
https://www.ncbi.nlm.nih.gov/pubmed/22424930
http://dx.doi.org/10.1016/j.devcel.2012.01.005
Descripción
Sumario:The advent of reprogramming and its impact on stem cell biology has renewed interest in lineage restriction in mammalian embryos, the source of embryonic (ES), epiblast (EpiSC), trophoblast (TS), and extraembryonic endoderm (XEN) stem cell lineages. Isolation of specific cell types during stem cell differentiation and reprogramming, and also directly from embryos, is a major technical challenge because few cell-surface proteins are known that can distinguish each cell type. We provide a large-scale proteomic resource of cell-surface proteins for the four embryo-derived stem cell lines. We validated 27 antibodies against lineage-specific cell-surface markers, which enabled investigation of specific cell populations during ES-EpiSC reprogramming and ES-to-XEN differentiation. Identified markers also allowed prospective isolation and characterization of viable lineage progenitors from blastocysts by flow cytometry. These results provide a comprehensive stem cell proteomic resource and enable new approaches to interrogate the mechanisms that regulate cell fate specification.