《口腔颌面外科杂志》 ›› 2023, Vol. 33 ›› Issue (3): 138-147. doi: 10.3969/j.issn.1005-4979.2023.03.002

• 基础研究 • 上一篇    下一篇

LincRNA-EPS对牙周炎小鼠肠道菌群影响的实验研究

陈栋怡(), 苏俭生()   

  1. 上海牙组织修复与再生工程技术研究中心,同济大学口腔医学院,同济大学附属口腔医院口腔修复科,上海 200072
  • 修回日期:2023-05-09 接受日期:2022-08-17 出版日期:2023-06-28 发布日期:2023-06-28
  • 通讯作者: 苏俭生,教授.E-mail:sjs@tongji.edu.cn
  • 作者简介:
    陈栋怡,硕士研究生.E-mail:
  • 基金资助:
    国家自然科学基金(81873715); 国家自然科学基金(82170913); 上海市科学技术委员会项目(201409006200)

LincRNA-EPS on intestinal flora of mice with periodontitis: An experimental study

CHEN Dongyi(), SU Jiansheng()   

  1. Shanghai Engineering Research Center of Tooth Restoration and Regeneration, Department of Prosthodontics, School and Hospital of Stomatology, Tongji University, Shanghai 200072, China
  • Revised:2023-05-09 Accepted:2022-08-17 Online:2023-06-28 Published:2023-06-28

摘要:

目的:探究基因间长链非编码RNA-EPS(long intergenic noncoding RNA-EPS, lincRNA-EPS)对牙周炎小鼠肠道菌群的影响。方法:选用8周龄雄性C57BL/6野生型小鼠和lincRNA-EPS基因敲除小鼠,分为野生型对照组(N组即group 1, n=6)、敲除型对照组(Nplus组即group 2, n=6)、野生型牙周炎组(P组即group 3, n=6)和敲除型牙周炎组(Pplus组即group 4, n=5)。对group 3及group 4小鼠采用丝线结扎法构建牙周炎模型,结扎10 d后收集各组小鼠粪便样品,采用16S rDNA测序技术分析各组小鼠肠道菌群的组成和结构。使用微型CT(micro-CT)检测野生型小鼠和lincRNA-EPS基因敲除小鼠上颌磨牙区的形态。结果:16S rDNA测序结果显示,lincRNA-EPS基因敲除牙周炎小鼠与野生型牙周炎小鼠的肠道菌群α多样性差异不明显(P>0.05),2组β多样性差异具有统计学意义(P<0.05)。在门水平及属水平上,两者物种组成及丰度差异具有统计学意义(P<0.05)。结论:lincRNA-EPS在一定程度上能够改变牙周炎小鼠肠道菌群的构成,其具体机制有待进一步研究。

关键词: 长链非编码RNA-EPS, 牙周炎, 肠道菌群, 高通量测序, 16S rDNA

Abstract:

Objective: To investigate the effect of long intergenic noncoding RNA-EPS (lincRNA-EPS) on intestinal flora in mice with periodontitis. Methods: 8-week-old male C57BL/6 wild-type mice and lincRNA-EPS knockout mice were selected and divided into wild-type control group (group N, i.e. group 1, n=6), knockout control group (group Nplus, i.e. group 2, n=6), wild-type periodontitis group (group P, i.e. group 3, n=6), and knockout periodontitis group (group Pplus, i.e. group 4, n=5). The periodontitis model was established in mice group 3 and group 4 by silk ligation, and fecal samples were collected from each group after 10 d of ligation, then 16S rDNA sequencing was applied to analyze the composition and structure of the intestinal flora of each group. Micro-CT was used to detect the morphology of the maxillary molar region in each group. Results: 16S rDNA sequencing showed that the lincRNA-EPS knockout mice had no significant difference in the α diversity of intestinal flora compared with wild-type periodontitis mice (P>0.05), and the β diversity was significantly different (P<0.05). The species composition and their abundance were significantly different at the phylum and genus levels (P<0.05). Conclusion: lincRNA-EPS can change the composition of intestinal flora in mice with periodontitis to some extent. Further studies are required to develop conclusions regarding the performance.

Key words: long intergenic noncoding RNA-EPS, periodontitis, intestinal flora, high-throughput sequencing, 16S rDNA

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