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供体的年龄会影响培养的人牙髓干细胞的性质。

Age of the donor affects the nature of cultured human dental pulp stem cells.

作者信息

Alzer Heba, Kalbouneh Heba, Alsoleihat Firas, Abu Shahin Nisreen, Ryalat Soukaina, Alsalem Mohammad, Alahmad Hazem, Tahtamouni Lubna

机构信息

Department of Conservative Dentistry, School of Dentistry, the University of Jordan, Amman 11942, Jordan.

Department of Anatomy and Histology, School of Medicine, the University of Jordan, Amman 11942, Jordan.

出版信息

Saudi Dent J. 2021 Nov;33(7):524-532. doi: 10.1016/j.sdentj.2020.09.003. Epub 2020 Sep 24.

Abstract

OBJECTIVES

The dental pulp stem cells (DPSCs) of six donors (three young donors aged < 19 years and three adult donors aged > 25 and < 30 years) were characterized for their stem cell marker expression and differentiation potential to study the effect of donor age on DPSCs .

METHODS

DPSCs were cultured in αMEM supplemented with 20% fetal calf serum (conventional conditions) or on fibronectin-coated flasks with neurobasal medium supplemented with B27, bFGF and EGF (alternative conditions). DPSCs were characterized by immunofluorescence staining to detect the neural crest/mesenchymal stem cells markers P75 and CD146, respectively. The differentiation potential was tested by the induction of DPSCs into osteogenic, adipogenic and glial lineages and then by detecting the corresponding markers osteocalcin, lipidtox and S100ß, respectively.

RESULTS

The DPSCs of the young donors expressed CD146 only under the conventional conditions and expressed P75 regardless of the culture conditions. However, the DPSCs of adult donors expressed CD146 only under the alternative conditions and expressed P75 only under conventional conditions. Only the DPSCs of the young donors differentiated into the glial linage. The DPSCs of the adult donors differentiated more efficiently into the adipogenic linage. Osteogenic differentiation was comparable.

CONCLUSION

Donor age affects the expression of stem cell markers and differentiation potential of DPSCs. Moreover, the effect of culture conditions on DPSCs is age dependent.

摘要

目的

对6名供体(3名年龄小于19岁的年轻供体和3名年龄大于25岁且小于30岁的成年供体)的牙髓干细胞(DPSCs)进行干细胞标志物表达和分化潜能的鉴定,以研究供体年龄对DPSCs的影响。

方法

将DPSCs培养于添加20%胎牛血清的αMEM培养基中(传统条件),或培养于包被纤连蛋白的培养瓶中,培养基为添加B27、碱性成纤维细胞生长因子(bFGF)和表皮生长因子(EGF)的神经基础培养基(替代条件)。通过免疫荧光染色对DPSCs进行鉴定,分别检测神经嵴/间充质干细胞标志物P75和CD146。通过将DPSCs诱导分化为成骨、成脂和神经胶质谱系,然后分别检测相应标志物骨钙素、Lipidtox和S100β,来测试其分化潜能。

结果

年轻供体的DPSCs仅在传统条件下表达CD146,且无论培养条件如何均表达P75。然而,成年供体的DPSCs仅在替代条件下表达CD146,仅在传统条件下表达P75。只有年轻供体的DPSCs分化为神经胶质谱系。成年供体的DPSCs更有效地分化为成脂谱系。成骨分化相当。

结论

供体年龄影响DPSCs的干细胞标志物表达和分化潜能。此外,培养条件对DPSCs的影响具有年龄依赖性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8769/8589584/70294b6711ef/gr1.jpg

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