Tang Jia, Saito Takashi
Division of Clinical Cariology, Department of Oral Rehabilitation, School of Dentistry, Health Sciences University of Hokkaido, Ishikari-Tobetsu, Hokkaido, Japan.
Division of Clinical Cariology, Department of Oral Rehabilitation, School of Dentistry, Health Sciences University of Hokkaido, Ishikari-Tobetsu, Hokkaido, Japan.
J Endod. 2017 Feb;43(2):263-271. doi: 10.1016/j.joen.2016.10.028.
The present study investigated the in vitro effects of nephronectin (Npnt) on the proliferation, differentiation, and mineralization of a rat odontoblast-like cell line (MDPC-23 cells).
MDPC-23 cells were cultured on Npnt-coated polystyrene or in the presence of soluble Npnt. Cell proliferation was analyzed using a Cell Counting Kit-8 kit (Dojindo, Kumamoto, Japan). Alkaline phosphatase (ALP) activity was quantified using an ALP activity assay. A reverse-transcription polymerase chain reaction was performed to evaluate the messenger RNA (mRNA) expression level of odontogenic markers and integrin(s). Alizarin red staining was conducted to quantify the calcium deposition.
Soluble Npnt had no adverse effect on the proliferation of MDPC-23 cells, but it exhibited concentration-dependent inhibitory activity toward differentiation. In contrast, coated Npnt promoted cell proliferation dramatically and significantly up-regulated the mRNA expression of odontogenesis-related genes; moreover, mRNA expression of integrin α1, α3, α5, β1, and β5 was found to be augmented. MDPC-23 cells cultured on Npnt-coated polystyrene displayed markedly higher ALP activity as early as day 3 after inoculation. In addition, mineralization was accelerated on Npnt-coated polystyrene.
Npnt in its immobilized form enhanced the proliferation of MDPC-23 cells and induced this odontoblastic precursor cell line to differentiate into a mineralizing phenotype.
本研究调查了肾连蛋白(Npnt)对大鼠成牙本质细胞样细胞系(MDPC-23细胞)增殖、分化和矿化的体外影响。
将MDPC-23细胞培养在包被有Npnt的聚苯乙烯上或在可溶性Npnt存在的条件下。使用细胞计数试剂盒-8(日本熊本同仁化学研究所)分析细胞增殖。使用碱性磷酸酶(ALP)活性测定法定量ALP活性。进行逆转录聚合酶链反应以评估牙源性标志物和整合素的信使核糖核酸(mRNA)表达水平。进行茜素红染色以定量钙沉积。
可溶性Npnt对MDPC-23细胞的增殖没有不利影响,但对分化表现出浓度依赖性抑制活性。相比之下,包被的Npnt显著促进细胞增殖并显著上调牙源性相关基因的mRNA表达;此外,发现整合素α1、α3、α5、β1和β5的mRNA表达增加。接种后第3天,在包被有Npnt的聚苯乙烯上培养的MDPC-23细胞显示出明显更高的ALP活性。此外,在包被有Npnt的聚苯乙烯上矿化加速。
固定化形式的Npnt增强了MDPC-23细胞的增殖,并诱导这种成牙本质细胞前体细胞系分化为矿化表型。