{"title":"miR-134 Up-Regulates Matrix Metalloproteinase 9 (MMP9) in Chronic Sinusitis","authors":"W. Cao, Yuanzhou Liu, Yandan Chen","doi":"10.1166/jbt.2023.3206","DOIUrl":null,"url":null,"abstract":"Chronic sinusitis is an upper respiratory tract disease. miR-134 involves in several diseases. However, its regulatory mechanism in chronic sinusitis has not been assessed. We aim to explore miR-134’s role in chronic sinusitis and the possible mechanism. miR-134 and MMP9 level\n was measured in chronic sinusitis tissues and normal tissues. The co-expression of miR-134 and MMP9 in PHNECs was detected by immunofluorescence. MMP-9 expression and IκB and α protein phosphorylation was detected by western blot. Immunofluorescence showed positive\n MMP-9 expression in epithelial cells. miR-134 level was significantly elevated in patients with chronic sinusitis and was co-localized with MMP-9 in the CRSwNP sample of epithelial cells. miR-134 up-regulated MMP-9, which was inhibited after addition of inhibitor BAY 11-7082. In conclusion,\n miR-134 up-regulates MMP-9 through NF-κB signaling to mediate the occurrence of chronic sinusitis, indicating that miR-134 may participate in the tissue remodeling of chronic sinusitis.","PeriodicalId":15300,"journal":{"name":"Journal of Biomaterials and Tissue Engineering","volume":" ","pages":""},"PeriodicalIF":0.1000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Biomaterials and Tissue Engineering","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1166/jbt.2023.3206","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Chronic sinusitis is an upper respiratory tract disease. miR-134 involves in several diseases. However, its regulatory mechanism in chronic sinusitis has not been assessed. We aim to explore miR-134’s role in chronic sinusitis and the possible mechanism. miR-134 and MMP9 level
was measured in chronic sinusitis tissues and normal tissues. The co-expression of miR-134 and MMP9 in PHNECs was detected by immunofluorescence. MMP-9 expression and IκB and α protein phosphorylation was detected by western blot. Immunofluorescence showed positive
MMP-9 expression in epithelial cells. miR-134 level was significantly elevated in patients with chronic sinusitis and was co-localized with MMP-9 in the CRSwNP sample of epithelial cells. miR-134 up-regulated MMP-9, which was inhibited after addition of inhibitor BAY 11-7082. In conclusion,
miR-134 up-regulates MMP-9 through NF-κB signaling to mediate the occurrence of chronic sinusitis, indicating that miR-134 may participate in the tissue remodeling of chronic sinusitis.