Zhang Q B, Zhang Z Q, Fang S L, Liu Y R, Jiang G, Li K F
Key Laboratory of Oral Medicine, Guangzhou Institute of Oral Disease, Stomatology Hospital of Guangzhou Medical University, Guangzhou, Guangdong Province, China
Department of Stomatology, The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong Province, China.
Genet Mol Res. 2014 Dec 4;13(4):10204-14. doi: 10.4238/2014.December.4.15.
Changes in oxygen concentration may influence various innate characteristics of stem cells. The effects of varying oxygen concentration on human periodontal ligament stem cells (HPDLSCs) has not been explored, particularly under hypoxia-related conditions. First, HPDLSCs were cultured from the periodontium of human teeth using the outgrowth method. STRO-1 and CD146 expression of HPDLSCs was investigated by flow cytometry. To detect the multilineage differentiation capacities of HPDLSCs, osteogenic-like and adipogenic-like states were induced in cells. Next, HPDLSCs (passage 3) were exposed to normal oxygen (21% O2) or hypoxia (2% O2) conditions for 7 days and cell proliferation was evaluated. After culture in osteogenic medium for 7 days, osteoblastic differentiation was evaluated by semi-quantitative reverse transcription-polymerase chain reaction analysis to detect 3 osteoblastic markers: core-binding factor a 1/runt-related transcription factor 2, osteocalcin, and osteopontin. In addition, each cell group was incubated with a hydroxyapatite/tricalcium phosphate carrier and transplanted subcutaneously into the back of immunocompromised mice to investigate transplantation differences in vivo. HPDLSCs were isolated, cultured, and successfully identified. After exposure of HPDLSCs to hypoxia for 7 days, the proliferation rate was increased and showed higher osteogenic differentiation potential compared to control cells. After 12 weeks of transplantation, hypoxia-treated HPDLSCs differentiated into osteoblast-like cells that formed bone-like structures. These results suggest that oxygen concentrations affect various aspects of HPDLSC physiology and that hypoxia enhances osteogenic differentiation both in vivo and in vitro. Oxygen concentration may be a critical parameter for HPDLSCs during expansion and differentiation.
氧浓度的变化可能会影响干细胞的各种固有特性。不同氧浓度对人牙周膜干细胞(HPDLSCs)的影响尚未得到研究,尤其是在与缺氧相关的条件下。首先,采用组织块培养法从人牙齿的牙周组织中培养HPDLSCs。通过流式细胞术检测HPDLSCs的STRO-1和CD146表达。为了检测HPDLSCs的多向分化能力,在细胞中诱导成骨样和成脂样状态。接下来,将第3代HPDLSCs暴露于正常氧(21% O₂)或缺氧(2% O₂)条件下7天,并评估细胞增殖情况。在成骨培养基中培养7天后,通过半定量逆转录-聚合酶链反应分析检测3种成骨细胞标志物:核心结合因子a 1/ runt相关转录因子2、骨钙素和骨桥蛋白,以评估成骨细胞分化情况。此外,将每个细胞组与羟基磷灰石/磷酸三钙载体孵育,并皮下移植到免疫缺陷小鼠的背部,以研究体内移植差异。HPDLSCs被分离、培养并成功鉴定。HPDLSCs暴露于缺氧环境7天后,其增殖率增加,与对照细胞相比,具有更高的成骨分化潜能。移植12周后,经缺氧处理的HPDLSCs分化为形成骨样结构的成骨样细胞。这些结果表明,氧浓度会影响HPDLSC生理学的各个方面,缺氧在体内和体外均能增强成骨分化。氧浓度可能是HPDLSCs在扩增和分化过程中的一个关键参数。