首页> 外文期刊>Journal of Endodontics: Official Journal of American Association of Endodontists >Isolation and Characterization of Human Dental Pulp Stem Cells from Cryopreserved Pulp Tissues Obtained from Teeth with Irreversible Pulpitis
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Isolation and Characterization of Human Dental Pulp Stem Cells from Cryopreserved Pulp Tissues Obtained from Teeth with Irreversible Pulpitis

机译:从不可逆性牙髓炎牙齿冷冻保存的牙髓组织中分离人牙髓干细胞的特性

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Introduction: Human dental pulp stem cells (DPSCs). are becoming an attractive target for therapeutic purposes because of their neural crest origin and propensity. Although DPSCs can be successfully cryopreserved, there are hardly any reports on cryopreservation of dental pulp tissues obtained from teeth diagnosed with symptomatic irreversible pulpitis during endodontic treatment and isolation and characterization of DPSCs from such cryopreserved pulp. The aim of this study was to cryopreserve the said pulp tissues to propagate and characterize isolated DPSCs. Methods: A medium consisting of 90% fetal bovine serum and 10% dimethyl sulfoxide was used for cryopreservation of pulp tissues. DPSCs were isolated from fresh and cryopreserved pulp tissues using an enzymatic method. Cell viability and proliferation were determined using the MIT [3,4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assay. DPSC migration and interaction were analyzed with the wound healing assay. Mesenchymal characteristics of DPSCs were verified by flow cytometric analysis of cell surface CD markers. The osteogenic and adipogenic potential of DPSCs was shown by von Kossa and oil red 0 staining methods, respectively, and the polymerase chain reaction method. Result: We found no significant difference in CD marker expression and osteogenic and adipogenic differentiation potential of DPSCs obtained from fresh and cryopreserved dental pulp tissue. Conclusions: Our study shows that dental pulp can be successfully cryopreserved without losing normal characteristics and differentiation potential of their DPSCs, thus making them suitable for dental banking and future therapeutic purposes.
机译:简介:人类牙髓干细胞(DPSC)。由于其神经c起源和倾向,正成为用于治疗目的的有吸引力的靶标。尽管可以成功地冷冻保存DPSC,但几乎没有任何关于在牙髓治疗期间从被诊断为有症状的不可逆性牙髓炎的牙齿获得的牙髓组织进行冷冻保存以及从这种冷冻保存的牙髓中分离和鉴定DPSC的报道。该研究的目的是冷冻保存所述牙髓组织,以繁殖和鉴定分离的DPSC。方法:使用由90%胎牛血清和10%二甲基亚砜组成的培养基冷冻保存牙髓组织。使用酶法从新鲜的和冷冻保存的纸浆组织中分离出DPSC。使用MIT [3,4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑]测定细胞活力和增殖。用伤口愈合试验分析DPSC的迁移和相互作用。 DPSC的间充质特征通过细胞表面CD标记的流式细胞术分析得到证实。 von Kossa和油红0染色法以及聚合酶链反应法分别显示了DPSC的成骨和成脂潜力。结果:我们发现新鲜和冷冻保存的牙髓组织中的DPSCs的CD标志物表达以及成骨和成脂分化潜能均无显着差异。结论:我们的研究表明,牙髓可以成功地冷冻保存而不会失去其DPSC的正常特性和分化潜能,从而使其适合牙科治疗和将来的治疗用途。

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