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TheraCal LC处理的人乳牙牙髓细胞的时间依赖性反应:与MTA相比的基因相互作用功能分析

Time-Dependent Response of Human Deciduous Tooth-Derived Dental Pulp Cells Treated with TheraCal LC: Functional Analysis of Gene Interactions Compared to MTA.

作者信息

Nam Ok Hyung, Kim Jae-Hwan, Choi Sung Chul, Kim Young

机构信息

Department of Pediatric Dentistry, School of Dentistry, Kyung Hee University, Seoul 02447, Korea.

Department of Pediatric Dentistry, School of Dentistry, Chonnam National University, Gwangju 61186, Korea.

出版信息

J Clin Med. 2020 Feb 15;9(2):531. doi: 10.3390/jcm9020531.

Abstract

Pulp capping material should facilitate hard tissue regeneration on the injured pulp tissue. TheraCal LC (TC) was recently developed. Although TC has shown reliable clinical outcomes after direct pulp capping, there are still remaining concerns regarding its detrimental effect on pulp cells. Therefore, this study aimed to identify the gene expression of human deciduous tooth-derived dental pulp cells exposed to TC compared to mineral trioxide aggregate (MTA). The cells were cultured and exposed to TC and MTA for 24 and 72 h. Next, total RNA was isolated. QuantSeq 3' mRNA-sequencing was used to examine differentially expressed genes (DEGs) in exposed to TC and MTA. Functional analysis of DEGs was performed using bioinformatics analysis. In gene ontology (GO) functional enrichment analysis, cells in TC for 24 h presented significantly enriched immune response ( < 0.001) and inflammatory response ( < 0.01) compared to MTA. TC showed enriched positive regulation of cell migration at 72 h ( < 0.001). In Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis, neuroactive ligand-receptor interaction ( = 1.19 × 10) and calcium signaling pathway ( = 2.96 × 10) were confirmed in the shared DEGs in TC. In conclusion, DEGs in TC may be involved in pathways associated with osteoclastogenesis and osteoclastic differentiation.

摘要

牙髓盖髓材料应有助于损伤牙髓组织的硬组织再生。TheraCal LC(TC)是最近研发的。尽管TC在直接盖髓后已显示出可靠的临床效果,但人们仍对其对牙髓细胞的有害影响存在担忧。因此,本研究旨在确定与三氧化矿物凝聚体(MTA)相比,暴露于TC的人乳牙来源的牙髓细胞的基因表达。将细胞培养并分别暴露于TC和MTA 24小时和72小时。接下来,提取总RNA。使用QuantSeq 3' mRNA测序来检测暴露于TC和MTA中的差异表达基因(DEG)。使用生物信息学分析对DEG进行功能分析。在基因本体(GO)功能富集分析中,与MTA相比,暴露于TC 24小时的细胞呈现出显著富集的免疫反应(<0.001)和炎症反应(<0.01)。TC在72小时时显示出细胞迁移的正调控富集(<0.001)。在京都基因与基因组百科全书(KEGG)分析中,在TC的共享DEG中证实了神经活性配体-受体相互作用(=1.19×10)和钙信号通路(=2.96×10)。总之,TC中的DEG可能参与与破骨细胞生成和破骨细胞分化相关的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78f5/7074006/9654d67957ee/jcm-09-00531-g001.jpg

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