• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

人牙龈上皮细胞对伴放线放线杆菌反应时白细胞介素-1β和白细胞介素-8的表达

Expression of IL-1 beta and IL-8 by human gingival epithelial cells in response to Actinobacillus actinomycetemcomitans.

作者信息

Uchida Y, Shiba H, Komatsuzawa H, Takemoto T, Sakata M, Fujita T, Kawaguchi H, Sugai M, Kurihara H

机构信息

Department of Periodontology and Endodontology, Hiroshima University Faculty of Dentistry, 1-2-3, Kasumi, Minami-ku, Hiroshima, Japan, 734-8553.

出版信息

Cytokine. 2001 May 7;14(3):152-61. doi: 10.1006/cyto.2001.0863.

DOI:10.1006/cyto.2001.0863
PMID:11396993
Abstract

The interaction between epithelial cells and microorganisms is the most important step in bacterial infections. Epithelial cells in response to exposure to pathogenic bacteria produce cytokines that initiate inflammation. However, little is known about the cytokine response of gingival epithelial cells to periodontopathogenic bacteria. Actinobacillus actinomycetemcomitans is thought to play a significant role in the initiation of periodontitis because of its bacteriological characteristics. In the present study, we investigated the cytokine induction by human gingival epithelial cells (HGEC) following exposure to A. actinomycetemcomitans in comparison with human gingival fibroblasts (HGF) in culture. Northern blot analysis showed that mRNAs of interleukin 1beta (IL-1beta) and IL-8, but not IL-6, in HGEC were induced in response to A. actinomycetemcomitans. Secretion of IL-8 by HGEC was also increased following A. actinomycetemcomitans challenge, whereas production of IL-1beta could not be detected. The levels of IL-8 and its mRNA were increased depending on the concentration of A. actinomycetemcomitans. The co-culture with HGF and A. actinomycetemcomitans resulted in an increase in the levels of IL-6 and IL-8 mRNA in HGF. However, HGF exposed to A. actinomycetemcomitans, showed no expression of IL-1beta mRNA. These findings demonstrated that HGEC and HGF stimulated with A. actinomycetemcomitans have different profiles in cytokine mRNA expression. Furthermore, A. actinomycetemcomitans may play an important role in amplifying the local immune response and in initiating inflammatory reaction through release of IL-8 from gingival epithelial cells.

摘要

上皮细胞与微生物之间的相互作用是细菌感染中最重要的步骤。上皮细胞在接触病原菌后会产生引发炎症的细胞因子。然而,关于牙龈上皮细胞对牙周病原菌的细胞因子反应却知之甚少。由于其细菌学特性,伴放线放线杆菌被认为在牙周炎的起始过程中起重要作用。在本研究中,我们将培养的人牙龈上皮细胞(HGEC)与人类牙龈成纤维细胞(HGF)相比较,研究了它们在接触伴放线放线杆菌后细胞因子的诱导情况。Northern印迹分析表明,HGEC中的白细胞介素1β(IL-1β)和IL-8的mRNA会因接触伴放线放线杆菌而被诱导,但IL-6的mRNA不会。在伴放线放线杆菌攻击后,HGEC分泌的IL-8也增加了,而未检测到IL-1β的产生。IL-8及其mRNA的水平会根据伴放线放线杆菌的浓度而增加。HGF与伴放线放线杆菌共培养导致HGF中IL-6和IL-8 mRNA水平增加。然而,接触伴放线放线杆菌的HGF未显示IL-1β mRNA的表达。这些发现表明,受伴放线放线杆菌刺激的HGEC和HGF在细胞因子mRNA表达方面具有不同的特征。此外,伴放线放线杆菌可能通过从牙龈上皮细胞释放IL-8在放大局部免疫反应和引发炎症反应中起重要作用。

相似文献

1
Expression of IL-1 beta and IL-8 by human gingival epithelial cells in response to Actinobacillus actinomycetemcomitans.人牙龈上皮细胞对伴放线放线杆菌反应时白细胞介素-1β和白细胞介素-8的表达
Cytokine. 2001 May 7;14(3):152-61. doi: 10.1006/cyto.2001.0863.
2
Irsogladine maleate influences the response of gap junctional intercellular communication and IL-8 of human gingival epithelial cells following periodontopathogenic bacterial challenge.马来酸伊索拉定影响牙周病原菌攻击后人牙龈上皮细胞间隙连接细胞间通讯及白细胞介素-8的反应。
Biochem Biophys Res Commun. 2005 Jul 29;333(2):502-7. doi: 10.1016/j.bbrc.2005.05.147.
3
Gingival fibroblast cytokine profiles in Actinobacillus actinomycetemcomitans-associated periodontitis.伴放线放线杆菌相关性牙周炎中牙龈成纤维细胞的细胞因子谱
J Periodontol. 1996 Sep;67(9):871-8. doi: 10.1902/jop.1996.67.9.871.
4
Irsogladine maleate abolishes the increase in interleukin-8 levels caused by outer membrane protein 29 from Aggregatibacter (Actinobacillus) actinomycetemcomitans through the ERK pathway in human gingival epithelial cells.马来酸异索拉定通过细胞外调节蛋白激酶(ERK)途径消除牙龈卟啉单胞菌外膜蛋白29引起的人牙龈上皮细胞白细胞介素-8水平升高。
J Periodontal Res. 2008 Oct;43(5):508-13. doi: 10.1111/j.1600-0765.2007.01059.x. Epub 2008 Jun 28.
5
Gingival epithelial cells increase interleukin-8 secretion in response to Actinobacillus actinomycetemcomitans challenge.牙龈上皮细胞在受到伴放线放线杆菌攻击时会增加白细胞介素-8的分泌。
J Periodontol. 1998 Oct;69(10):1105-10. doi: 10.1902/jop.1998.69.10.1105.
6
Differential regulation of innate immune response genes in gingival epithelial cells stimulated with Aggregatibacter actinomycetemcomitans.伴放线聚集杆菌刺激牙龈上皮细胞中固有免疫反应基因的差异调节
J Periodontal Res. 2008 Feb;43(1):116-23. doi: 10.1111/j.1600-0765.2007.00998.x. Epub 2007 Nov 13.
7
Irsogladine maleate regulates neutrophil migration and E-cadherin expression in gingival epithelium stimulated by Aggregatibacter actinomycetemcomitans.马来酸依地普仑调节牙龈上皮细胞中被伴放线放线杆菌刺激的中性粒细胞迁移和 E-钙黏蛋白表达。
Biochem Pharmacol. 2010 May 15;79(10):1496-505. doi: 10.1016/j.bcp.2010.01.017. Epub 2010 Jan 22.
8
Regulation of IL-8 by Irsogladine maleate is involved in abolishment of Actinobacillus actinomycetemcomitans-induced reduction of gap-junctional intercellular communication.马来酸伊索拉定对白细胞介素-8的调节作用参与消除伴放线放线杆菌诱导的缝隙连接细胞间通讯减少。
Cytokine. 2006 Jun;34(5-6):271-7. doi: 10.1016/j.cyto.2006.06.002. Epub 2006 Jul 25.
9
Expression of beta-defensin-2 in human gingival epithelial cells in response to challenge with Porphyromonas gingivalis in vitro.体外牙龈卟啉单胞菌刺激下人牙龈上皮细胞中β-防御素-2的表达
J Periodontal Res. 2006 Aug;41(4):334-9. doi: 10.1111/j.1600-0765.2006.00879.x.
10
Differential effects of five Aggregatibacter actinomycetemcomitans strains on gingival epithelial cells.五种伴放线聚集杆菌菌株对牙龈上皮细胞的不同影响。
Oral Microbiol Immunol. 2008 Dec;23(6):455-8. doi: 10.1111/j.1399-302X.2008.00449.x.

引用本文的文献

1
Advances in modeling periodontal host-microbe interactions: insights from organotypic and organ-on-chip systems.牙周宿主-微生物相互作用建模的进展:来自器官型和芯片器官系统的见解。
Lab Chip. 2025 Feb 25;25(5):1342-1371. doi: 10.1039/d4lc00871e.
2
Transcriptome Analysis of Porphyromonas gingivalis Lipopolysaccharide-Induced Early Gene Expression in Human Gingival Keratinocytes.牙龈卟啉单胞菌脂多糖诱导人牙龈角质形成细胞早期基因表达的转录组分析
J Periodontal Res. 2025 Apr;60(4):380-391. doi: 10.1111/jre.13353. Epub 2024 Oct 16.
3
Topical Application of Dexamethasone-Loaded Core-Multishell Nanocarriers Against Oral Mucosal Inflammation.
载地塞米松的核-多壳纳米载体局部应用于对抗口腔黏膜炎症
Macromol Biosci. 2024 Dec;24(12):e2400286. doi: 10.1002/mabi.202400286. Epub 2024 Oct 3.
4
Obesity Is Associated with a Weakened Gingival Inflammatory Cytokine Response.肥胖与牙龈炎症细胞因子反应减弱有关。
Medicina (Kaunas). 2023 Nov 28;59(12):2089. doi: 10.3390/medicina59122089.
5
Cytokines secreted by inflamed oral mucosa: implications for oral cancer progression.炎症性口腔黏膜分泌的细胞因子:对口腔癌进展的影响
Oncogene. 2023 Apr;42(15):1159-1165. doi: 10.1038/s41388-023-02649-y. Epub 2023 Mar 6.
6
Differential immune responses of 3D gingival and periodontal connective tissue equivalents to microbial colonization.3D牙龈和牙周结缔组织替代物对微生物定植的差异性免疫反应。
J Tissue Eng. 2022 Jul 29;13:20417314221111650. doi: 10.1177/20417314221111650. eCollection 2022 Jan-Dec.
7
Lactobacilli Attenuate the Effect of Infection in Gingival Epithelial Cells.乳酸杆菌减弱牙龈上皮细胞感染的影响。
Front Microbiol. 2022 May 4;13:846192. doi: 10.3389/fmicb.2022.846192. eCollection 2022.
8
Periodontal inflamed surface area in oral cavity associated with febrile neutropenia in patients with hematologic malignancy undergoing chemotherapy.口腔内牙周炎炎症表面面积与接受化疗的血液恶性肿瘤患者发热性中性粒细胞减少症相关。
Sci Rep. 2022 Feb 15;12(1):2483. doi: 10.1038/s41598-022-06485-0.
9
Nrf2 in the Field of Dentistry with Special Attention to NLRP3.牙科领域中的Nrf2,特别关注NLRP3。
Antioxidants (Basel). 2022 Jan 12;11(1):149. doi: 10.3390/antiox11010149.
10
Expression of Interleukin-1ß and Interleukin-8 in Oral Potentially Malignant Disorders and Carcinomas.白细胞介素-1β和白细胞介素-8在口腔潜在恶性疾病和癌中的表达
Front Oral Health. 2021 Sep 10;2:649406. doi: 10.3389/froh.2021.649406. eCollection 2021.