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Human Dental Pulp Stem Cells – Isolation and Long Term Cultivation

机译:人类牙髓干细胞–分离和长期培养

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Human adult mesenchymal stem cells (MSCs) are rare elements living in various organs (e.g. bone marrow, skeletal muscle), with capability to differentiate in various cell types (e.g. chondrocytes, adipocytes and osteoblasts). In the year 2000, Gronthos and co-workers isolated stem cells from the human dental pulp (DPSCs). Later on, stem cells from exfoliated tooth were also obtained. The aims of our study were to establish protocol of DPSCs isolation and to cultivate DPSCs either from adult or exfoliated tooth, and to compare these cells with mesenchymal progenitor cell (MPCs) cultures. MPCs were isolated from the human bone marrow of proximal femur. DPSCs were isolated from deciduous and permanent teeth. Both cell types were cultivated under the same conditions in the media with 2 % of FCS supplemented with PDGF and EGF growth factors. We have cultivated undifferentiated DPSCs for long time, over 60 population doublings in cultivation media designed for bone marrow MPCs. After reaching Hayflick’s limit, they still have normal karyotype. Initial doubling time of our cultures was from 12 to 50 hours for first 40 population doublings, after reaching 50 population doublings, doubling time had increased to 60–90 hours. Regression analysis of uncumulated population doublings proved tight dependence of population doublings on passage number and slow decrease of proliferation potential. In comparison with bone marrow MPCs, DPSCs share similar biological characteristics and stem cell properties. The results of our experiments proved that the DPSCs and MPCs are highly proliferative, clonogenic cells that can be expanded beyond Hayflick’s limit and remain cytogenetically stable. Moreover we have probably isolated two different populations of DPSCs. These DPSCs lines differed one from another in morphology. Because of their high proliferative and differentiation potential, DPSCs can become more attractive, easily accessible source of adult stem cells for therapeutic purposes.
机译:人类成年间充质干细胞(MSC)是生活在各种器官(例如骨髓,骨骼肌)中的稀有元素,具有在各种细胞类型(例如软骨细胞,脂肪细胞和成骨细胞)中分化的能力。在2000年,Gronthos及其同事从人类牙髓(DPSC)中分离了干细胞。后来,还获得了来自脱落牙齿的干细胞。我们研究的目的是建立分离DPSC的协议,并从成年或脱落的牙齿中培养DPSC,并将这些细胞与间充质祖细胞(MPC)培养物进行比较。从股骨近端的人骨髓中分离出MPC。 DPSC是从乳牙和恒牙中分离出来的。两种细胞类型均在相同条件下于添加了PDGF和EGF生长因子的2%FCS培养基中培养。我们长期以来一直在培养未分化的DPSC,在为骨髓MPC设计的培养基中,有超过60倍的人口翻倍。达到Hayflick的极限后,他们仍然具有正常的核型。我们的文化最初的倍增时间是前40个人口倍增从12到50个小时,达到50个人口倍增之后,倍增时间增加到60-90小时。对未累积种群倍增的回归分析证明,种群倍增对通过次数的严格依赖性和扩散潜能的缓慢降低。与骨髓MPC相比,DPSC具有相似的生物学特性和干细胞特性。我们的实验结果证明,DPSC和MPC是高度增殖的克隆性细胞,可以扩展到Hayflick的极限之外,并保持细胞遗传学稳定性。此外,我们可能已经隔离了两个不同的DPSC群体。这些DPSC线在形态上彼此不同。由于其高的增殖和分化潜能,DPSCs可以成为更具吸引力,易于获得的成人干细胞来源,用于治疗目的。

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