Kwon Se Yun, Chun So Young, Ha Yun-Sok, Kim Dae Hwan, Kim Jeongshik, Song Phil Hyun, Kim Hyun Tae, Yoo Eun Sang, Kim Bum Soo, Kwon Tae Gyun
1Department of Urology, School of Medicine, Dongguk University, 123 Dongdae-ro, Gyeongju, 38066 Korea.
2BioMedical Research Institute, Kyungpook National University Hospital, 130 Dongdeok-ro, Jung-gu, Daegu, 41944 Korea.
Tissue Eng Regen Med. 2017 Jul 31;14(5):595-604. doi: 10.1007/s13770-017-0068-8. eCollection 2017 Oct.
Atmospheric () oxygen pressure is around 150 mm Hg (20% O), whereas physiologic () oxygen pressure ranges between 5 and 50 mm Hg (0.7-7% O). The normoxic environment in cell culture does not refer to a physiological stem cell niche. The aim of this study is to investigate the effect of oxygen concentration on cell properties of human mesenchymal stem cells (MSCs). We analyzed cell proliferation rate, senescence, immunophenotype, stemness gene expression and differentiation potency with human urine stem cells (USCs), dental pulp stem cells (DPSCs), amniotic fluid stem cells (AFSCs), and bone marrow stromal cells (BMSCs). USCs, DPSCs, AFSCs and BMSCs were cultured under either 5% O hypoxic or 20% O normoxic conditions for 5 days. MSCs cultured under hypoxia showed significantly increased proliferation rate and high percentage of S-phase cells, compared to normoxic condition. In real-time PCR assay, the cells cultured under hypoxia expressed higher level of Oct4, C-Myc, Nanog, Nestin and HIF-1α. In immunophenotype analysis, MSCs cultured under hypoxia maintained higher level of the MSC surface markers, and lower hematopoietic markers. Senescence was inhibited under hypoxia. Hypoxia enhances osteogenic differentiation efficiency compared to normoxia. Hypoxia showed enhanced cell proliferation rate, retention of stem cell properties, inhibition of senescence, and increased differentiation ability compared to normoxia.
大气()氧分压约为150毫米汞柱(20% O),而生理()氧分压范围在5至50毫米汞柱之间(0.7 - 7% O)。细胞培养中的常氧环境并非指生理干细胞龛。本研究的目的是探讨氧浓度对人间充质干细胞(MSC)细胞特性的影响。我们用人尿干细胞(USC)、牙髓干细胞(DPSC)、羊水干细胞(AFSC)和骨髓基质细胞(BMSC)分析了细胞增殖率、衰老、免疫表型、干性基因表达和分化潜能。USC、DPSC、AFSC和BMSC在5% O低氧或20% O常氧条件下培养5天。与常氧条件相比,低氧培养的MSC显示出显著提高的增殖率和高比例的S期细胞。在实时PCR分析中,低氧培养的细胞Oct4、C-Myc、Nanog、Nestin和HIF-1α表达水平更高。在免疫表型分析中,低氧培养的MSC维持较高水平的MSC表面标志物和较低水平的造血标志物。低氧条件下衰老受到抑制。与常氧相比,低氧增强了成骨分化效率。与常氧相比,低氧显示出增强的细胞增殖率、干细胞特性的保留、衰老的抑制以及分化能力的增加。