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炎症性颞下颌关节疼痛小鼠三叉神经节和三叉神经脊髓尾核的转录组分析

Transcriptomic Analysis of Trigeminal Ganglion and Spinal Trigeminal Nucleus Caudalis in Mice with Inflammatory Temporomandibular Joint Pain.

作者信息

Dong Tieli, Si Haichao, Li Zhisong, Bai Qian, Tao Feng

机构信息

Department of Anesthesiology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, People's Republic of China.

Department of Anesthesiology, Nanyang Central Hospital, Nanyang, People's Republic of China.

出版信息

J Pain Res. 2022 May 23;15:1487-1502. doi: 10.2147/JPR.S364887. eCollection 2022.

Abstract

BACKGROUND

Persistent facial pain heavily impacts the quality of life in patients with temporomandibular joint (TMJ) disorders. Previous studies have demonstrated that long non-coding ribonucleic acid (lncRNA) is an important regulator of pain. In this study, we aimed to analyze lncRNA expression in the whole transcriptome of trigeminal ganglia (TG) and spinal trigeminal nucleus caudalis (Sp5C) in a chronic inflammatory TMJ pain mouse model.

METHODS

Chronic inflammatory TMJ pain was induced by intra-TMJ injection of complete Freund's adjuvant (CFA). Mouse TG and Sp5C tissues were harvested on day 4 after CFA injection. The lncRNA expression patterns in the whole transcriptome of TG and Sp5C were profiled with RNA sequencing.

RESULTS

We observed that 38 lncRNAs and 849 mRNAs were differentially expressed after CFA treatment. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analysis further revealed relationships among those differentially expressed lncRNAs and mRNAs and their potential functions. Specific categories of biological process, cellular processes, and molecular function of the differentially expressed transcripts were ascertained.

CONCLUSION

Our results suggest that lncRNA expression in the whole transcriptome of trigeminal nociceptive system could contribute to the molecular mechanisms that underlie chronic inflammatory TMJ pain.

摘要

背景

持续性面部疼痛严重影响颞下颌关节(TMJ)紊乱患者的生活质量。先前的研究表明,长链非编码核糖核酸(lncRNA)是疼痛的重要调节因子。在本研究中,我们旨在分析慢性炎性颞下颌关节疼痛小鼠模型中三叉神经节(TG)和三叉神经脊束核尾侧亚核(Sp5C)全转录组中的lncRNA表达情况。

方法

通过向颞下颌关节内注射完全弗氏佐剂(CFA)诱导慢性炎性颞下颌关节疼痛。在注射CFA后第4天采集小鼠的TG和Sp5C组织。采用RNA测序分析TG和Sp5C全转录组中的lncRNA表达模式。

结果

我们观察到CFA处理后有38种lncRNA和849种mRNA差异表达。基因本体论和京都基因与基因组百科全书分析进一步揭示了这些差异表达的lncRNA和mRNA之间的关系及其潜在功能。确定了差异表达转录本的特定生物学过程、细胞过程和分子功能类别。

结论

我们的结果表明,三叉神经伤害感受系统全转录组中的lncRNA表达可能有助于慢性炎性颞下颌关节疼痛的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f84/9141904/5669078ac9bf/JPR-15-1487-g0001.jpg

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