Al-Hassiny Ahmad, Hussaini Haizal, Milne Trudy, Seo Benedict, Rich Alison M, Friedlander Lara T
Sir John Walsh Research Institute, Faculty of Dentistry, University of Otago, New Zealand.
Eur Endod J. 2019 Apr 4;4(2):80-85. doi: 10.14744/eej.2019.26349. eCollection 2019.
ABSTRACT.
This study aimed to examine the protein and gene expression of vascular endothelial growth factor (VEGF) and angiopoietins-1 and 2 in tissue from healthy and inflamed dental pulps.
Permanent teeth with pulps diagnosed as healthy or reversible pulpitis were used for immunohistochemistry (IHC) and gene expression experiments. For IHC, a whole pulp tissue was excavated from the pulp chamber, and it was formalin-fixed and processed for routine IHC with angiogenic markers anti-VEGF, anti-Ang1, and anti-Ang2. Staining was visualized with diaminobenzidine (DAB), and examined using light microscopy. The distribution of markers in healthy and inflamed pulps was qualitatively and quantitatively analyzed. Real-time quantitative polymerase chain reaction (RT qPCR) was used to ascertain the gene expression levels of , , and in the presence of inflammation. Statistical analysis was performed using the Mann-Whitney test with the statistical significance level set at 0.05.
There was increased protein and mRNA expression of VEGF and Ang-1 markers in inflamed pulp samples as compared with that in the healthy pulp tissue. IHC demonstrated intense expression of the VEGF protein on endothelial cells (EC) and some non-ECs, and there was significantly more staining on ECs associated with inflamed tissue (P<0.001). Ang-1 and Ang-2 were significantly expressed on ECs and non-ECs (P<0.05). RT qPCR did not show significant differences in gene expression between healthy and inflamed samples although similar trends were observed to IHC.
The presence of Ang-1, Ang-2, VEGF, and gene in healthy and mildly inflamed pulp tissue associated with reversible pulpitis indicates that these angiogenic factors may participate in physiological and pathological angiogenesis and healing. The inflammatory process may regulate Ang-1/Ang2/Tie2 signaling; and together with VEGF, these growth factors have an important role in modulating pulp angiogenesis.
摘要。
本研究旨在检测健康牙髓和炎症牙髓组织中血管内皮生长因子(VEGF)、血管生成素 -1和血管生成素 -2的蛋白质及基因表达情况。
将诊断为健康牙髓或可复性牙髓炎的恒牙用于免疫组织化学(IHC)和基因表达实验。对于免疫组织化学,从髓腔中取出整个牙髓组织,用福尔马林固定,并使用抗VEGF、抗Ang1和抗Ang2等血管生成标记物进行常规免疫组织化学处理。用二氨基联苯胺(DAB)显色,并用光学显微镜检查。对健康牙髓和炎症牙髓中标记物的分布进行定性和定量分析。采用实时定量聚合酶链反应(RT qPCR)确定炎症状态下VEGF、Ang-1和Ang-2的基因表达水平。使用Mann-Whitney检验进行统计分析,设定统计学显著性水平为0.05。
与健康牙髓组织相比,炎症牙髓样本中VEGF和Ang-1标记物的蛋白质和mRNA表达增加。免疫组织化学显示VEGF蛋白在内皮细胞(EC)和一些非内皮细胞上有强烈表达,与炎症组织相关的内皮细胞上的染色明显更多(P<0.001)。Ang-1和Ang-2在内皮细胞和非内皮细胞上均有显著表达(P<0.05)。尽管观察到与免疫组织化学有相似趋势,但实时定量聚合酶链反应(RT qPCR)未显示健康样本和炎症样本之间基因表达有显著差异。
在与可复性牙髓炎相关的健康和轻度炎症牙髓组织中存在Ang-1、Ang-2、VEGF和Tie2基因,表明这些血管生成因子可能参与生理和病理血管生成及愈合过程。炎症过程可能调节Ang-1/Ang2/Tie2信号通路;并且这些生长因子与VEGF一起在调节牙髓血管生成中起重要作用。