Activation of p38, p21, and NRF-2 Mediates Decreased Proliferation of Human Dental Pulp Stem Cells Cultured under 21% O2

被引:39
作者
El Alami, Marya [1 ]
Vina-Almunia, Jose [2 ]
Gambini, Juan [1 ]
Mas-Bargues, Cristina [1 ]
Siow, Richard C. M. [3 ]
Penarrocha, Miguel [2 ]
Mann, Giovanni E. [3 ]
Borras, Consuelo [1 ]
Vina, Jose [1 ]
机构
[1] Univ Valencia, Fac Med, Dept Physiol, Valencia 46010, Spain
[2] Univ Valencia, Fac Med, Dept Odontol, Valencia 46010, Spain
[3] Kings Coll London, British Heart Fdn, Ctr Res Excellence, Sch Med,Div Cardiovasc, London SE1 9NH, England
关键词
REACTIVE OXYGEN; BONE-MARROW; REGENERATIVE MEDICINE; BLOOD-FLOW; HYPOXIA; TISSUE; EXPRESSION; DISEASE; DIFFERENTIATION; P21(WAF1/CIP1);
D O I
10.1016/j.stemcr.2014.08.002
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
High rates of stem cell proliferation are important in regenerative medicine and in stem cell banking for clinical use. Ambient oxygen tensions (21% O-2) are normally used for in vitro culture, but physiological levels in vivo range between 3% and 6% O-2. We compared proliferation of human dental pulp stem cells (hDPSCs) cultured under 21% versus 3% O-2. The rate of hDPSC proliferation is significantly lower at 21% O-2 compared to physiological oxygen levels due to enhanced oxidative stress. Under 21% O-2, increased p38 phosphorylation led to activation of p21. Increased generation of reactive oxygen species and p21 led to activation of the NRF-2 signaling pathway. The upregulation of NRF-2 antioxidant defense genes under 21% O-2 may interact with cell-cycle-related proteins involved in regulating cell proliferation. Activation of p38/p21/NRF-2 in hDPSCs cultured under ambient oxygen tension inhibits stem cell proliferation and upregulates NRF-2 antioxidant defenses.
引用
收藏
页码:566 / 573
页数:8
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