Reprogramming the Pluripotent Cell Cycle: Restoration of an Abbreviated G1 Phase in Human Induced Pluripotent Stem (iPS) Cells

被引:68
作者
Ghule, Prachi N. [1 ,2 ]
Medina, Ricardo [1 ,2 ]
Lengner, Christopher J. [3 ]
Mandeville, Matthew [1 ,2 ]
Qiao, Meng [1 ,2 ]
Dominski, Zbigniew [4 ,5 ]
Lian, Jane B. [1 ,2 ]
Stein, Janet L. [1 ,2 ]
Van Wijnen, Andre J. [1 ,2 ]
Stein, Gary S. [1 ,2 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Cell Biol, Worcester, MA 01655 USA
[2] Univ Massachusetts, Sch Med, Ctr Canc, Worcester, MA 01655 USA
[3] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[4] Univ N Carolina, Dept Biochem & Biophys, Chapel Hill, NC USA
[5] Univ N Carolina, Program Mol Biol & Biotechnol, Chapel Hill, NC 27599 USA
关键词
HUMAN SOMATIC-CELLS; SUBNUCLEAR ORGANIZATION; GENE-REGULATION; HINF-P; EXPRESSION; FIBROBLASTS; NPAT; PHOSPHORYLATION; P220(NPAT); GENERATION;
D O I
10.1002/jcp.22440
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Induced pluripotent stem (iPS) cells derived from terminally differentiated human fibroblasts are reprogrammed 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. hES cells are characterized by an abbreviated G1 phase (similar to 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 [5-bromo-2'-deoxy-uridine (BrdU) incorporation], cell cycle distribution (FACS analysis and Ki67 staining) and subnuclear organization of HLBs [immunofluorescence microscopy and fluorescence in situ hybridization (FISH)] revealed that human iPS cells have a short G1 phase (similar to 2.5 h) and an abbreviated cell cycle (16-18 h). Furthermore, HLBs are formed and reorganized rapidly after mitosis (within 1.5-2 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. J. Cell. Physiol. J. Cell. Physiol. 226: 1149-1156, 2011. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:1149 / 1156
页数:8
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