{"title":"Effect of NF-κB on endothelial damage mediated by inflammatory cytokines in Kawasaki disease","authors":"Jinrong Fu, Chengrong Li, Yufeng Zhou","doi":"10.3760/CMA.J.ISSN.0578-1310.2002.02.104","DOIUrl":null,"url":null,"abstract":"Objective \nKawasaki disease (KD) is the leading cause of acquired heart diseases in children. Its etiology is unknown. In recent years, data have shown that the dysfunction of T cell and monocytes/macrophages plays a central role in the development of vasculitis. Nuclear factor-κB(NF-κB) is positioned to integrate information from immune signaling pathway that can regulate the function of T cell and monocytes/macrophages. But the role of NF-κB in endothelial damage of KD is unknown. Therefore, the objective of the study was to further explore the effects of NF-κB on the endothelial damage in KD. \n \n \nMethods \nHuman umbilical vein endothelial cells were cultured in vitro and the production of tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β) and interleukin-6 (IL-6) were measured by enzyme-linked immunosorbent assay ( ELISA). The proportion of apoptotic cells in endothelial cells induced by the supernatants of peripheral blood mononuclear cells (PBMCs) was detected by AnnexinⅤ/PI double-staining. Electrophoretic mobility shift assay (EMSA) was used to detect the activity of NF-κB. \n \n \nResults \nThe levels of TNF-α, IL-1β and IL-6 were markedly increased in patients and the proportion of apoptotic cells in endothelial cells induced by the cultured supernatants of PBMCs was markedly elevated (38.45±7.80)% compared to (2.87±0.76)% in the control subjects. The apoptosis induced by the supernatants of cultured PBMCs could be reversed, to some degree, through alone anti- TNF-α, IL-1β or IL-6 monoclonal antibody (McAb), or the combination together. The activity of NF-κB in the activated PBMCs in patients with KD was distinctly increased and SN50, the blockade of NF-κB, could significantly inhibit the production of TNF-α, IL-1β, IL-6 and the apoptosis of endothelial cells induced by the supernatants of cultured PBMC. \n \n \nConclusion \nNF-κB, which can trigger the transcription of inflammatory cytokines such, as TNF-α, IL-1β, IL-6, plays an important role in endothelial damage of KD. \n \n \nKey words: \nMucocutaneous lymph node synrome; NF-κB; Cytokine; Endothelium, rascular","PeriodicalId":416525,"journal":{"name":"Chinexe Journal of Pediatrics","volume":"96 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2002-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinexe Journal of Pediatrics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3760/CMA.J.ISSN.0578-1310.2002.02.104","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Objective
Kawasaki disease (KD) is the leading cause of acquired heart diseases in children. Its etiology is unknown. In recent years, data have shown that the dysfunction of T cell and monocytes/macrophages plays a central role in the development of vasculitis. Nuclear factor-κB(NF-κB) is positioned to integrate information from immune signaling pathway that can regulate the function of T cell and monocytes/macrophages. But the role of NF-κB in endothelial damage of KD is unknown. Therefore, the objective of the study was to further explore the effects of NF-κB on the endothelial damage in KD.
Methods
Human umbilical vein endothelial cells were cultured in vitro and the production of tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β) and interleukin-6 (IL-6) were measured by enzyme-linked immunosorbent assay ( ELISA). The proportion of apoptotic cells in endothelial cells induced by the supernatants of peripheral blood mononuclear cells (PBMCs) was detected by AnnexinⅤ/PI double-staining. Electrophoretic mobility shift assay (EMSA) was used to detect the activity of NF-κB.
Results
The levels of TNF-α, IL-1β and IL-6 were markedly increased in patients and the proportion of apoptotic cells in endothelial cells induced by the cultured supernatants of PBMCs was markedly elevated (38.45±7.80)% compared to (2.87±0.76)% in the control subjects. The apoptosis induced by the supernatants of cultured PBMCs could be reversed, to some degree, through alone anti- TNF-α, IL-1β or IL-6 monoclonal antibody (McAb), or the combination together. The activity of NF-κB in the activated PBMCs in patients with KD was distinctly increased and SN50, the blockade of NF-κB, could significantly inhibit the production of TNF-α, IL-1β, IL-6 and the apoptosis of endothelial cells induced by the supernatants of cultured PBMC.
Conclusion
NF-κB, which can trigger the transcription of inflammatory cytokines such, as TNF-α, IL-1β, IL-6, plays an important role in endothelial damage of KD.
Key words:
Mucocutaneous lymph node synrome; NF-κB; Cytokine; Endothelium, rascular