Oct4 expression is not required for mouse somatic stem cell self-renewal

被引:331
作者
Lengner, Christopher J.
Camargo, Fernando D.
Hochedlinger, Konrad
Welstead, G. Grant
Zaidi, Sarnir
Gokhale, Surnita
Scholer, Hans R.
Tomilin, Alexey
Jaenisch, Rudolf [1 ]
机构
[1] MIT, Whitehead Inst Biomed Res, Cambridge Ctr 9, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02142 USA
[3] Massachusetts Gen Hosp, Ctr Canc, Boston, MA 02114 USA
[4] Harvard Stem Cell Inst, Ctr Regenerat Med, Boston, MA 02114 USA
[5] Max Planck Inst Mol Biomed, Dept Cell & Dev Biol, D-48149 Munster, Germany
[6] Russian Acad Sci, Inst Cytol, St Petersburg 194064, Russia
关键词
D O I
10.1016/j.stem.2007.07.020
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The Pou domain containing transcription factor Oct4 is a well-established regulator of pluripotency in the inner cell mass of the mammalian blastocyst as well as in embryonic stem cells. While it has been shown that the Oct4 gene is inactivated through a series of epigenetic modifications following implantation, recent studies have detected Oct4 activity in a variety of somatic stem cells and tumor cells. Based on these observations it has been suggested that Oct4 may also function in maintaining self-renewal of somatic stem cells and, in addition, may promote tumor formation. We employed a genetic approach to determine whether Oct4 is important for maintaining pluripotency in the stem cell compartments of several somatic tissues, including the intestinal epithelium, bone marrow (hematopoietic and mesenchymal lineages), hair follicle, brain, and liver. Oct4 gene ablation in these tissues revealed no abnormalities in homeostasis or regenerative capacity. We conclude that Oct4 is dispensable for both self-renewal and maintenance of somatic stem cells in the adult mammal.
引用
收藏
页码:403 / 415
页数:13
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