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Increased expression of epha7 in inflamed human dental pulp

机译:epha7在发炎的人类牙髓中的表达增加

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Introduction: Pulpitis has been associated with abundant inflammatory cells, dilated blood vessels, and thickening nerve fibers histopathologically with or without severe pain clinically. On the basis of EphA7 receptor expression in inflammatory cells, the developing mouse dental pulp, and trigeminal nerve system, EphA7 may possibly be involved in local inflammatory response and sensory innervation of adult dental pulp as well as odontogenic pain conducted through the trigeminal system. The purpose of the study was to analyze the expression of EphA7 gene in healthy and inflamed human dental pulps and to elucidate the roles of EphA7 gene in dental pulp inflammation response and odontogenic pain. Methods: Twelve healthy controls, 5 acute pulpitis from dental trauma, 21 symptomatic, and 20 asymptomatic irreversible pulpitis human dental pulps were involved in the study. The protein expression, subcellular localization, and mRNA level of EphA7 gene were detected by immunohistochemistry and real-time reverse transcriptase-polymerase chain reaction, respectively. Results: In healthy samples, immunohistochemical staining showed positive EphA7 expression only in vascular endothelial cells and odontoblasts with cytoplasm staining. Under inflammatory conditions, in addition to the above cells, EphA7 staining began to occur in fibroblasts, nerve fiber tissues, and inflammatory cells. Compared with healthy samples, EphA7 expressions at both mRNA and protein levels increased significantly in acute and irreversible pulpitis samples. In asymptomatic irreversible pulpitis samples, EphA7 expressions were significantly lower than those in symptomatic ones but still higher than those in healthy ones. There was no significant difference between acute and symptomatic irreversible pulpitis groups. Conclusions: The results suggest that EphA7 gene may be a marker reflecting inflammatory activity and pain state for human dental pulp.
机译:简介:在临床上,无论有无严重疼痛,在组织病理学上,牙髓炎都会与大量炎症细胞,血管扩张和神经纤维增厚相关。根据EphA7受体在炎症细胞,发育中的小鼠牙髓和三叉神经系统中的表达,EphA7可能参与成人牙髓的局部炎症反应和感觉神经支配以及通过三叉神经系统进行的牙源性疼痛。这项研究的目的是分析EphA7基因在健康和发炎的人类牙髓中的表达,并阐明EphA7基因在牙髓炎症反应和牙源性疼痛中的作用。方法:12名健康对照者,5名来自牙齿创伤的急性牙髓炎,21例有症状的和20例无症状的不可逆性牙髓炎的人类牙髓参与了研究。通过免疫组织化学和实时逆转录酶-聚合酶链反应分别检测EphA7基因的蛋白表达,亚细胞定位和mRNA水平。结果:在健康样本中,免疫组织化学染色仅在具有细胞质染色的血管内皮细胞和成牙本质细胞中显示EphA7阳性表达。在炎症条件下,除上述细胞外,EphA7染色开始在成纤维细胞,神经纤维组织和炎症细胞中发生。与健康样品相比,急性和不可逆性牙髓炎样品中EphA7在mRNA和蛋白水平上的表达均显着增加。在无症状的不可逆性牙髓炎样本中,EphA7的表达明显低于有症状的,但仍高于健康的。急性和有症状的不可逆性牙髓炎组之间无显着差异。结论:结果提示EphA7基因可能是反映人类牙髓炎性活性和疼痛状态的标志物。

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