Nahm Kyung-Yen, Heo Jung Sun, Lee Jae-Hyung, Lee Dong-Yeol, Chung Kyu-Rhim, Ahn Hyo-Won, Kim Seong-Hun
Department of Orthodontics, School of Dentistry, Kyung Hee University, 26 Kyunghee-daero, Dongdaemun-gu, Seoul 130-701, Republic of Korea.
Department of Maxillofacial Biomedical Engineering and Institute of Oral Biology, School of Dentistry, Kyung Hee University, 26 Kyunghee-daero, Dongdaemun-gu, Seoul 130-701, Republic of Korea.
Biomed Res Int. 2015;2015:538080. doi: 10.1155/2015/538080. Epub 2015 Feb 11.
This study aimed to evaluate the genes that were expressed in the healing bones around SLA-treated titanium orthodontic mini-implants in a beagle at early (1-week) and late (4-week) stages with RNA-sequencing (RNA-Seq). Samples from sites of surgical defects were used as controls. Total RNA was extracted from the tissue around the implants, and an RNA-Seq analysis was performed with Illumina TruSeq. In the 1-week group, genes in the gene ontology (GO) categories of cell growth and the extracellular matrix (ECM) were upregulated, while genes in the categories of the oxidation-reduction process, intermediate filaments, and structural molecule activity were downregulated. In the 4-week group, the genes upregulated included ECM binding, stem cell fate specification, and intramembranous ossification, while genes in the oxidation-reduction process category were downregulated. GO analysis revealed an upregulation of genes that were related to significant mechanisms, including those with roles in cell proliferation, the ECM, growth factors, and osteogenic-related pathways, which are associated with bone formation. From these results, implant-induced bone formation progressed considerably during the times examined in this study. The upregulation or downregulation of selected genes was confirmed with real-time reverse transcription polymerase chain reaction. The RNA-Seq strategy was useful for defining the biological responses to orthodontic mini-implants and identifying the specific genetic networks for targeted evaluations of successful peri-implant bone remodeling.
本研究旨在通过RNA测序(RNA-Seq)评估比格犬在早期(1周)和晚期(4周)阶段,经喷砂酸蚀处理的正畸微型钛种植体周围愈合骨中表达的基因。手术缺损部位的样本用作对照。从种植体周围组织中提取总RNA,并使用Illumina TruSeq进行RNA-Seq分析。在1周组中,细胞生长和细胞外基质(ECM)基因本体(GO)类别的基因上调,而氧化还原过程、中间丝和结构分子活性类别的基因下调。在4周组中,上调的基因包括ECM结合、干细胞命运决定和膜内成骨,而氧化还原过程类别的基因下调。GO分析显示与重要机制相关的基因上调,包括在细胞增殖、ECM、生长因子和成骨相关途径中起作用的基因,这些都与骨形成有关。从这些结果来看,在本研究检测的时间段内,种植体诱导的骨形成有显著进展。通过实时逆转录聚合酶链反应证实了所选基因的上调或下调。RNA-Seq策略有助于确定正畸微型种植体的生物学反应,并识别特定的基因网络,以便对种植体周围骨组织成功重塑进行靶向评估。