Differentially Expressed Genes in Dental Pulp Tissues of Individuals With Symptomatic Irreversible Pulpitis With and Without History of COVID-19

被引:2
|
作者
Cho, Han Na [1 ]
de Souza, Leticia Chaves [1 ]
Johnson, Cleverick [2 ]
Klein, John R. [3 ]
Kirkpatrick, Timothy C. [1 ]
Silva, Renato [4 ]
Letra, Ariadne [4 ,5 ,6 ,7 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Sch Dent, Dept Endodont, Houston, TX USA
[2] Univ Texas Hlth Sci Ctr Houston, Sch Dent, Dept Gen Practice & Dent Publ Hlth, Houston, TX USA
[3] Univ Texas Hlth Sci Ctr Houston, Sch Dent, Dept Diagnost & Biomed Sci, Houston, TX USA
[4] Univ Pittsburgh, Sch Dent Med, Dept Endodont, Pittsburgh, PA USA
[5] Univ Pittsburgh, Dept Oral & Craniofacial Sci, Sch Dent Med, Pittsburgh, PA USA
[6] Univ Pittsburgh, Ctr Craniofacial & Dent Genet, Sch Dent Med, Pittsburgh, PA USA
[7] Bridgeside Point I, Ctr Craniofacial & Dent Genet, Dept Oral & Craniofacial Sci, Dept Endodont, 100 Technol Dr,room 450L, Pittsburgh, PA 15219 USA
关键词
Dental pulp; COVID; inflammation; gene expression; VIRUS;
D O I
10.1016/j.joen.2023.05.002
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Introduction: Increased levels of proinflammatory markers have been reported in tissues of individuals with Coronavirus Disease 2019 (COVID-19). We hypothesize that inflamed dental pulp tissues of individuals with previous history of COVID-19 may present a differential inflammatory gene expression profile in comparison with individuals who never had COVID-19. Materials and Methods: Dental pulp tissues were collected from 27 individuals referred for endodontic treatment due to symptomatic irreversible pulpitis. Of these, 16 individuals had a history of COVID-19 (6 months to 1 year post infection) and 11 individuals had no previous history of COVID-19 (controls). Total RNA from pulp tissue samples was extracted and subjected to RNA sequencing for comparison of differentially expressed genes (DEGs) among groups. DEGs showing log2(fold change) > 1 or <-1, and P < .05 were considered significantly dysregulated. Results: RNA sequencing identified 1461 genes as differentially expressed among the groups. Of these, 311 were protein coding genes, 252 (81%) that were upregulated and 59 (19%) that were downregulated in the COVID group compared with controls. The top upregulated genes in the COVID group were HSFX1 (4.12-fold change) and LINGO3 (2.06-fold change); significantly downregulated genes were LYZ (-1.52-fold change), CCL15 and IL8 (-1.45-fold change). Conclusions: Differential gene expression in dental pulp tissues of COVID and non-COVID groups suggests potential contribution of COVID-19 on dysregulating inflammatory gene expression in the inflamed dental pulp. (J Endod 2023
引用
收藏
页码:799 / 807
页数:9
相关论文
共 4 条
  • [1] Differentially expressed immune response genes in COVID-19 patients based on disease severity
    Li, Shasha
    Duan, Xiaoqiong
    Li, Yujia
    Li, Ming
    Gao, Yong
    Li, Tuantuan
    Li, Shilin
    Tan, Lin
    Shao, Tuo
    Jeyarajan, Andre J.
    Chen, Limin
    Han, Mingfeng
    Lin, Wenyu
    Li, Xiuyong
    AGING-US, 2021, 13 (07): : 9265 - 9276
  • [2] Platelet dysfunction caused by differentially expressed genes as key pathogenic mechanisms in COVID-19
    Tan, Xiaoyong
    Gao, Xiaojun
    Zheng, Huanhuan
    Yuan, Hui
    Liu, Hong
    Ran, Qijun
    Luo, Mao
    MINERVA CARDIOLOGY AND ANGIOLOGY, 2024, 72 (05) : 517 - 534
  • [3] Drug-disease interactions of differentially expressed genes in COVID-19 liver samples: an in-silico analysis
    Rasool, Susan Omar
    Nahr, Ata Mirzaei
    Eskandari, Sania
    Hosseinzadeh, Milad
    Moghanloo, Soheila Asoudeh
    Ebrahimzadeh, Farnoosh
    INVESTIGACION CLINICA, 2021, 62 (04): : 316 - 324
  • [4] Single cell multi-omic analysis identifies key genes differentially expressed in innate lymphoid cells from COVID-19 patients
    Kaushik, Abhinav
    Chang, Iris
    Han, Xiaorui
    He, Ziyuan
    Komlosi, Zsolt I.
    Ji, Xuhuai
    Cao, Shu
    Akdis, Cezmi A.
    Boyd, Scott
    Pulendran, Bali
    Maecker, Holden T.
    Davis, Mark M.
    Chinthrajah, R. Sharon
    Dekruyff, Rosemarie H.
    Nadeau, Kari C.
    FRONTIERS IN IMMUNOLOGY, 2024, 15