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    Reprogramming the pluripotent cell cycle: restoration of an abbreviated G1 phase in human induced pluripotent stem (iPS) cells

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    Authors
    Ghule, Prachi N.
    Medina, Ricardo F.
    Lengner, Christopher Joachim
    Mandeville, Matthew
    Qiao, Meng
    Dominski, Zbigniew
    Lian, Jane B.
    Stein, Janet L.
    Stein, Gary S.
    Van Wijnen, Andre J.
    UMass Chan Affiliations
    Department of Cell Biology
    Document Type
    Journal Article
    Publication Date
    2011-03-01
    Keywords
    Induced Pluripotent Stem Cells
    Cell Cycle
    G1 Phase
    Cell Biology
    
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    Link to Full Text
    http://dx.doi.org/10.1002/jcp.22440
    Abstract
    Induced pluripotent stem (iPS) cells derived from terminally differentiated human fibroblasts are re-programmed to possess stem cell like properties. However, the extent to which iPS cells exhibit unique properties of the human embryonic stem (hES) cell cycle remains to be established. Human ES cells are characterized by an abbreviated G1 phase ( approximately 2.5 h) and accelerated organization of subnuclear domains that mediate the assembly of regulatory machinery for histone gene expression [i.e., histone locus bodies (HLBs)]. We therefore examined cell cycle parameters of iPS cells in comparison to hES cells. Analysis of DNA synthesis (BrdU incorporation), cell cycle distribution (FACS analysis and Ki67 staining) and subnuclear organization of HLBs [immuno-fluorescence microscopy and fluorescence in situ hybridization (FISH)] revealed that human iPS cells have a short G1 phase ( approximately 2.5 h) and an abbreviated cell cycle (16-18 h). Furthermore, HLBs are formed and reorganized rapidly after mitosis (within 0.5 to 1.5 h). Thus, reprogrammed iPS cells have cell cycle kinetics and dynamic subnuclear organization of regulatory machinery that are principal properties of pluripotent hES cells. Our findings support the concept that the abbreviated cell cycle of hES and iPS cells is functionally linked to pluripotency. (c) 2010 Wiley-Liss, Inc.
    Source
    J Cell Physiol. 2011 May;226(5):1149-56. doi: 10.1002/jcp.22440. Epub 2010 Oct 13. Link to article on publisher's site
    DOI
    10.1002/jcp.22440
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/49600
    PubMed ID
    20945438
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1002/jcp.22440
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