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与 2 型糖尿病相关牙周炎相关的独特基因和信号通路:初步研究。

Distinctive genes and signaling pathways associated with type 2 diabetes-related periodontitis: Preliminary study.

机构信息

Department of Periodontology, University of Florida College of Dentistry, Gainesville, FL, United States of America.

Department of Dentistry, Federal University of Rio Grande do Norte, Natal, RN, Brazil.

出版信息

PLoS One. 2024 Jan 19;19(1):e0296925. doi: 10.1371/journal.pone.0296925. eCollection 2024.

Abstract

The biological mechanisms underlying the pathogenesis of type 2 diabetes (T2DM)-related periodontitis remain unclear. This cross-sectional study evaluated the distinctive transcriptomic changes between tissues with periodontal health and with periodontitis in patients with T2DM. In this cross-sectional study, whole transcriptome sequencing was performed on gingival biopsies from non-periodontitis and periodontitis tissues from non-diabetic and diabetic patients. A differentially expressed gene (DEG) analysis and Ingenuity Pathway Analysis (IPA) assessed the genes and signaling pathways associated with T2DM-related periodontitis. Immunohistochemistry was performed to validate selected DEGs possibly involved in T2DM-related periodontitis. Four hundred and twenty and one thousand five hundred and sixty-three DEGs (fold change ≥ 2) were uniquely identified in the diseased tissues of non-diabetic and diabetic patients, respectively. The IPA predicted the activation of Phagosome Formation, Cardiac β-adrenergic, tRNA Splicing, and PI3K/AKT pathways. The IPA also predicted the inhibition of Cholesterol Biosynthesis, Adrenomedullin, and Inositol Phosphate Compounds pathways in T2DM-related periodontitis. Validation of DEGs confirmed changes in protein expression of PTPN2, PTPN13, DHCR24, PIK3R2, CALCRL, IL1RN, IL-6R and ITGA4 in diseased tissues in diabetic subjects. Thus, these preliminary findings indicate that there are specific genes and functional pathways that may be involved in the pathogenesis of T2DM-related periodontitis.

摘要

2 型糖尿病(T2DM)相关牙周炎发病机制的生物学机制尚不清楚。本横断面研究评估了 T2DM 患者牙周健康组织与牙周炎组织之间的独特转录组变化。在这项横断面研究中,对非牙周炎和非糖尿病患者牙周炎组织的牙龈活检进行了全转录组测序。差异表达基因(DEG)分析和 IPA 评估了与 T2DM 相关牙周炎相关的基因和信号通路。通过免疫组织化学验证了可能与 T2DM 相关牙周炎相关的选定 DEG。在非糖尿病和糖尿病患者的病变组织中分别唯一鉴定出 421 和 1563 个 DEG(倍数变化≥2)。IPA 预测了吞噬体形成、心脏β-肾上腺素能、tRNA 剪接和 PI3K/AKT 途径的激活。IPA 还预测了 T2DM 相关牙周炎中胆固醇生物合成、肾上腺髓质素和肌醇磷酸化合物途径的抑制。DEG 的验证证实了糖尿病患者病变组织中 PTPN2、PTPN13、DHCR24、PIK3R2、CALCRL、IL1RN、IL-6R 和 ITGA4 蛋白表达的变化。因此,这些初步发现表明,可能有特定的基因和功能途径参与 T2DM 相关牙周炎的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/361d/10798476/a3b11b41e4f4/pone.0296925.g001.jpg

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