Identification of microRNAs expressed in an animal model of periodontal disease and their impact on pathological processes

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Kelly de Almeida , Priscilla Câmara , Gabriela Camargo , Tiago Pereira , André Vieira , Iscia Lopes-Cendes , Patrícia Severino , Eliana B. Souto , Aislan Pascoal , Vinicius Pascoal
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Abstract

MicroRNAs represent a class of small RNAs that act to silence genes post-transcriptionally by inhibiting the translation of target messenger RNAs, and this study aimed to understand how miRNAs influence the set-up of periodontal disease. Periodontitis was induced by inserting a ligature into the left first mandibular molar in a rat model, which was kept for the entire 56 days-time of experiment. After 56 days post-periodontitis induction, the histopathological analysis showed an apical extension of the junctional epithelium, with areas of hyperplasia, exocytosis, and a mixed inflammatory infiltrate with a predominance of neutrophils, lymphocytes, and eventual plasma cells in the deeper layers. The cement surface showed areas of irregularity, covered by cementoblasts and irregular surfaces, confirming the set-up of periodontitis. In the sequencing analysis, 26,404 genes were identified, with 132 reaching statistical significance. Among genes with a statistical difference, 18 were found to encode for microRNAs. The identified microRNAs are primarily involved in bone remodeling by acting on fibroblast growth factors, and collagen production. These outcomes demonstrate a signaling role in bone resorption, which is consistent with the histopathological observations that show the installation of inflammation with epithelial migration and the beginning of the repair process, with cementum resorption. The disclosure of how miRNAs may influence the maintaining of periodontal disease will help the development of new dental materials for the prophylaxis and treatment of alveolar bone resorption.

鉴定牙周病动物模型中表达的微核糖核酸及其对病理过程的影响
本研究旨在了解 miRNA 如何影响牙周病的形成。通过在大鼠左侧第一下颌臼齿上插入结扎线诱发牙周炎,实验时间为56天。诱发牙周炎 56 天后,组织病理学分析表明,交界上皮向根尖延伸,有增生、外渗的区域,深层有混合性炎症浸润,以中性粒细胞、淋巴细胞和最终的浆细胞为主。骨水泥表面出现不规则区域,被骨水泥母细胞和不规则表面覆盖,证实了牙周炎的设置。在测序分析中,共鉴定出 26 404 个基因,其中 132 个具有统计学意义。在有统计学差异的基因中,发现 18 个基因编码 microRNA。已发现的 microRNA 主要通过作用于成纤维细胞生长因子和胶原蛋白的产生来参与骨重塑。这些结果表明,miRNA 在骨吸收过程中起着信号作用,这与组织病理学观察结果一致,即炎症的发生与上皮细胞的迁移以及修复过程的开始与骨水泥的吸收。揭示 miRNA 如何影响牙周病的维持,将有助于开发预防和治疗牙槽骨吸收的新型牙科材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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