Karamzadeh Razieh, Baghaban Eslaminejad Mohamadreza, Sharifi-Zarchi Ali
Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Cell J. 2017 Winter;18(4):609-618. doi: 10.22074/cellj.2016.4727. Epub 2016 Sep 26.
Pulp and periodontal tissues are well-known sources of mesenchymal stem cells (MSCs) that provide a promising place in tissue engineering and regenerative medicine. The molecular mechanisms underlying commitment and differentiation of dental stem cells that originate from different dental tissues are not fully understood. In this study, we have compared the expression levels of pluripotency factors along with immunological and developmentally-related markers in the culture of human dental pulp stem cells (hDPSCs), human dental follicle stem cells (hDFSCs), and human embryonic stem cells (hESCs).
In this experimental study, isolated human dental stem cells were investigated using quantitative polymerase chain reaction (qPCR), immunostaining, and fluorescence-activated cell sorting (FACS). Additionally, we conducted gene ontology (GO) analysis of differentially expressed genes and compared them between dental stem cells and pluripotent stem cells.
The results demonstrated that pluripotency ( and ) and immunological ( and ) factors had higher expressions in hDFSCs, with the exception of the ratio, and which expressed more in hDPSCs. Immunostaining of OCT4, and c-MYC showed cytoplasmic and nucleus localization in both groups at similar passages. GO analysis showed that the majority of hDFSCs and hDPSCs populations were in the synthesis (S) and mitosis (M) phases of the cell cycle, respectively.
This study showed different status of heterogeneous hDPSCs and hDFSCs in terms of stemness, differentiation fate, and cell cycle phases. Therefore, the different behaviors of dental stem cells should be considered based on clinical treatment variations.
牙髓和牙周组织是间充质干细胞(MSCs)的重要来源,在组织工程和再生医学领域具有广阔的应用前景。然而,源自不同牙齿组织的牙干细胞定向分化和分化的分子机制尚未完全明确。在本研究中,我们比较了人牙髓干细胞(hDPSCs)、人牙囊干细胞(hDFSCs)和人胚胎干细胞(hESCs)培养物中多能性因子以及免疫和发育相关标志物的表达水平。
在本实验研究中,采用定量聚合酶链反应(qPCR)、免疫染色和荧光激活细胞分选(FACS)技术对分离的人牙干细胞进行研究。此外,我们对差异表达基因进行了基因本体(GO)分析,并比较了牙干细胞和多能干细胞之间的差异。
结果表明,除了 比例外,多能性( 和 )和免疫( 和 )因子在hDFSCs中的表达较高,而 在hDPSCs中的表达更多。OCT4、 和c-MYC的免疫染色显示,在相似传代次数的两组细胞中,它们均定位于细胞质和细胞核。GO分析表明,大多数hDFSCs和hDPSCs群体分别处于细胞周期的合成(S)期和有丝分裂(M)期。
本研究表明,异质性hDPSCs和hDFSCs在干性、分化命运和细胞周期阶段方面存在不同状态。因此,在临床治疗中应根据牙干细胞的不同行为进行考虑。