Gong Ai-Xiu, Zhang Jing-Han, Li Jing, Wu Jun, Wang Lin, Miao Deng-Shun
Department of Stomatology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu 210008, P.R. China.
Department of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu 210008, P.R. China.
Int J Mol Med. 2017 Sep;40(3):647-660. doi: 10.3892/ijmm.2017.3065. Epub 2017 Jul 12.
There are anatomical and functional differences between human dental pulp (DP) and periodontal ligament (PDL). However, the molecular biological differences and function of these tissues are poorly understood. In the present study, we employed a cDNA microarray array to screen for differentially expressed genes (DEGs) between human DP and PDL tissues, and used the online software WebGestalt to perform the functional analysis of the DEGs. In addition, the STRING database and KEGG pathway analysis were applied for interaction network and pathway analysis of the DEGs. DP and PDL samples were obtained from permanent premolars (n=16) extracted for orthodontic purposes. The results of the microarray assay were confirmed by RT-qPCR. The DEGs were found to be significantly associated with the extracellular matrix and focal adhesion. A total of 10 genes were selected to confirm the results. The mRNA levels of integrin alpha 4 (ITGA4), integrin alpha 8 (ITGA8), neurexin 1 (NRXN1) and contactin 1 (CNTN1) were significantly higher in the DP than in the PDL tissues. However, the levels of collagen type XI alpha 1 (COL11A1), aggrecan (ACAN), collagen type VI alpha 1 (COL6A1), chondroadherin (CHAD), laminin gamma 2 (LAMC2) and laminin alpha 3 (LAMA3) were higher in the PDL than in the DP samples. The gene expression profiles provide novel insight into the characterization of DP and PDL tissues, and contribute to our understanding of the potential molecular mechanisms of dental tissue mineralization and regeneration.
人类牙髓(DP)和牙周膜(PDL)在解剖学和功能上存在差异。然而,这些组织的分子生物学差异和功能尚不清楚。在本研究中,我们采用cDNA微阵列筛选人DP和PDL组织之间的差异表达基因(DEGs),并使用在线软件WebGestalt对DEGs进行功能分析。此外,应用STRING数据库和KEGG通路分析对DEGs进行相互作用网络和通路分析。DP和PDL样本取自因正畸目的拔除的恒牙前磨牙(n = 16)。微阵列分析结果通过RT-qPCR得到证实。发现DEGs与细胞外基质和粘着斑显著相关。共选择10个基因来证实结果。整合素α4(ITGA4)、整合素α8(ITGA8)、神经纤连蛋白1(NRXN1)和接触蛋白1(CNTN1)的mRNA水平在DP中显著高于PDL组织。然而,Ⅺ型胶原α1(COL11A1)、聚集蛋白聚糖(ACAN)、Ⅵ型胶原α1(COL6A1)、软骨粘连蛋白(CHAD)、层粘连蛋白γ2(LAMC2)和层粘连蛋白α3(LAMA3)的水平在PDL中高于DP样本。基因表达谱为DP和PDL组织的特征提供了新的见解,并有助于我们理解牙齿组织矿化和再生的潜在分子机制。