The roles of Oct4 and Nanog in maintaining self-renewal and undifferentiated status of adult stem cells are unclear. Here, increase in Oct4 and Nanog expression along with increased proliferation and differentiation potential but decreased spontaneous differentiation were observed in early-passage (E), hypoxic culture (H), and p21 knockdown (p21KD) mesenchymal stem cells (MSCs) compared to late-passage (L), normoxic culture (N), and scrambled shRNA-overexpressed (Scr) MSCs. Knockdown of Oct4 and Nanog in E, H, and p21KD MSCs decreased proliferation and differentiation potential and enhanced spontaneous differentiation, whereas overexpression of Oct4 and Nanog in L, N, and Scr MSCs increased proliferation and differentiation potential and suppressed spontaneous differentiation. Oct4 and Nanog upregulate Dnmt1 through direct binding to its promoter, thereby leading to the repressed expression of p16 and p21 and genes associated with development and lineage differentiation. These data demonstrate the important roles of Oct4 and Nanog in maintaining MSC properties.
Although low-density culture provides an efficient method for rapid expansion of human mesenchymal stem cells (MSCs), MSCs enriched by this method undergo senescence and lose their stem cell properties, which could be preserved by combining low-density and hypoxic culture. The mechanism was mediated through direct down-regulation of E2A-p21 by the hypoxia-inducible factor-1␣ (HIF-1␣)-TWIST axis. Expansion under normoxia induced E2A and p21 expression, which were abrogated by overexpression of TWIST, whereas siRNA against TWIST up-regulated E2A and p21 in hypoxic cells. Furthermore, siRNA against p21 in normoxic cells enhanced proliferation and increased differentiation potential, whereas overexpression of p21 in hypoxic cells induced a decrease in proliferation and a loss of differentiation capacity. More importantly, MSCs expanded under hypoxic conditions by up to 100 population doublings, exhibited telomerase activity with maintained telomere length, normal karyotyping, and intact genetic integrity, and did not form tumors. These results support low-density hypoxic culture as a method for efficiently expanding MSCs without losing stem cell properties or increasing tumorigenicity. (Blood. 2011; 117(2):459-469) IntroductionHuman multipotent stromal cells or mesenchymal stem cells (MSCs), capable of self-renewal and differentiating into various mesenchymal tissues, 1 have emerged as a promising tool for clinical applications in, for example, cell-based therapy for osteogenesis imperfecta 2 and tissue engineering in cartilage and bone. 3 MSCs are also applied in cardiac therapeutics because they prevent deleterious remodeling and improve recovery. 4 However, variations in the isolation techniques, growth media, and culture conditions used cause a remarkable difference in their proliferation and differentiation capacity. 5 Furthermore, many studies have consistently noticed a senescent tendency of MSCs upon expansion. 6,7 Thus, the difference in stem cell properties and the senescence encountered during expansion hinder the clinical applications of MSCs.Hypoxia has been known to regulate several cellular processes and signal transductions via the expression of hypoxia inducible factor-1 (HIF-1), a heterodimer consisting of the constitutively expressed aryl hydrocarbon receptor nuclear translocator (ARNT) and the hypoxic response factor HIF-1␣. HIF-1␣ is regulated by the cellular O 2 concentration and determines the transcriptional activity of HIF-1. 8 Most of the effects of HIF-1␣ were investigated on cancer cells. HIF-1␣, induced during ischemia that occurred in the course of tumor progression or after treatment, stimulates proliferation 9 and induces vascular endothelial growth factor expression and angiogenesis. 9 Hypoxia has also been reported to enhance proliferation, survival, and dopaminergic differentiation of central nervous system (CNS) precursors. 10 In parallel, hypoxia also determines the cell fate of neural crest stem cells. 11 These findings suggest neural stem cells may exhibit a conserved response ...
Hyp also increased the levels of p-extracellular signal-regulated kinase (ERK), but there was a minimal effect on p-signal transducer and activator of transcription-3, and an inhibitor of the ERK1/2 pathway had no effect on hypoxiainduced apoptosis of the HAECs. The results are consistent with suggestions that administration of MSCs or factors secreted by MSCs may provide a therapeutic method of decreasing apoptosis and enhancing angiogenesis.
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