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纳米羟基磷灰石-二氧化硅-玻璃离子水门汀处理牙髓干细胞的早期牙源性分化

Early Odontogenic Differentiation of Dental Pulp Stem Cells Treated with Nanohydroxyapatite-Silica-Glass Ionomer Cement.

作者信息

Siew Ching Hii, Thirumulu Ponnuraj Kannan, Luddin Norhayati, Ab Rahman Ismail, Nik Abdul Ghani Nik Rozainah

机构信息

School of Dental Sciences, Universiti Sains Malaysia, Kubang Kerian 16150, Kelantan, Malaysia.

Human Genome Centre, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian 16150, Kelantan, Malaysia.

出版信息

Polymers (Basel). 2020 Sep 17;12(9):2125. doi: 10.3390/polym12092125.

Abstract

This study aimed to investigate the effects of nanohydroxyapatite-silica-glass ionomer cement (nanoHA-silica-GIC) on the differentiation of dental pulp stem cells (DPSCs) into odontogenic lineage. DPSCs were cultured in complete Minimum Essential Medium Eagle-Alpha Modification (-MEM) with or without nanoHA-silica-GIC extract and conventional glass ionomer cement (cGIC) extract. Odontogenic differentiation of DPSCs was evaluated by real-time reverse transcription polymerase chain reaction (rRT-PCR) for odontogenic markers: dentin sialophosphoprotein (), dentin matrix protein 1 (), osteocalcin (), osteopontin (), alkaline phosphatase (), collagen type I (), and runt-related transcription factor 2 () on day 1, 7, 10, 14, and 21, which were normalized to the house keeping gene glyceraldehyde-3-phosphate dehydrogenase (). Untreated DPSCs were used as a control throughout the study. The expressions of and were higher on days 7 and 10, that of on day 10, those of and on day 14, and that of on day 1; exhibited a time-dependent increase from day 7 to day 14. Despite the above time-dependent variations, the expressions were comparable at a concentration of 6.25 mg/mL between the nanoHA-silica-GIC and cGIC groups. This offers empirical support that nanoHA-silica-GIC plays a role in the odontogenic differentiation of DPSCs.

摘要

本研究旨在探讨纳米羟基磷灰石-二氧化硅-玻璃离子水门汀(nanoHA-二氧化硅-GIC)对牙髓干细胞(DPSCs)向牙源性谱系分化的影响。将DPSCs在含有或不含有nanoHA-二氧化硅-GIC提取物及传统玻璃离子水门汀(cGIC)提取物的完全α-改良伊格尔最低必需培养基(α-MEM)中培养。通过实时逆转录聚合酶链反应(rRT-PCR)检测牙源性标志物:牙本质涎磷蛋白()、牙本质基质蛋白1()、骨钙素()、骨桥蛋白()、碱性磷酸酶()、I型胶原()和 runt相关转录因子2()在第1、7、10、14和21天的表达,以看家基因甘油醛-3-磷酸脱氢酶()进行标准化。在整个研究中,未处理的DPSCs用作对照。在第7天和第10天,和的表达较高,在第10天,的表达较高,在第14天,和的表达较高,在第1天,的表达较高;从第7天到第14天,呈时间依赖性增加。尽管有上述时间依赖性变化,但在nanoHA-二氧化硅-GIC组和cGIC组中,6.25 mg/mL浓度下的表达相当。这为nanoHA-二氧化硅-GIC在DPSCs牙源性分化中发挥作用提供了实验依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae85/7569887/c05a49c02ca5/polymers-12-02125-g001.jpg

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