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  2. College of Oral Medicine /口腔醫學院
  3. Institute of Oral Sciences/口腔科學研究所
  4. Inhibitory effect of GMI, an immunomodulatory protein from <i>Ganoderma microsporum</i>, on myofibroblast activity and proinflammatory cytokines in human fibrotic buccal mucosal fibroblasts
 
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Inhibitory effect of GMI, an immunomodulatory protein from <i>Ganoderma microsporum</i>, on myofibroblast activity and proinflammatory cytokines in human fibrotic buccal mucosal fibroblasts

Journal
Environmental Toxicology
Journal Volume
33
Journal Issue
1
Start Page
32-40
ISSN
1520-4081
1522-7278
Date Issued
2017-10-06
Author(s)
Ping‐Hui Lee
Pei‐Ling Hsieh
Yi‐Wen Liao
Cheng‐Chia Yu  
DOI
10.1002/tox.22489
URI
https://scholars.csmu.edu.tw/handle/123456789/3037
Abstract
<jats:title>Abstract</jats:title><jats:p>Oral submucous fibrosis (OSF) has been indicated as one of the oral potentially malignant disorders. Epidemiological studies have attributed this pathological fibrosis to the habit of areca nuts chewing, which causes chronic inflammation and persistent activation of myofibroblasts in the oral cavity. Hence, it is crucial to find an effective intervention to ameliorate inflammation in order to prevent the malignant progression of OSF. In this study, we assessed the anti‐inflammatory effect of the immunomodulatory protein, GMI, extracted from <jats:italic>Ganoderma microsporum</jats:italic> on the expression proinflammatory cytokines and the myofibroblast characteristics in human fibrotic buccal mucosal fibroblasts (fBMFs). Our results demonstrated that the expression level of interleukin (IL)‐6 and IL‐8 were decreased after exposure of GMI and the myofibroblast activities, including collagen gel contraction, migration, invasion, and wound healing abilities were inhibited as well. Furthermore, we confirmed these findings in the arecoline‐stimulated BMFs. Consistent with the above findings, the expression of the myofibroblast marker α‐smooth muscle actin and other fibrogenic markers, such as type I collagen, fibronectin, and vimentin in fBMFs were all reduced in a dose‐dependent manner. Collectively, our data suggested that GMI suppressed the proinflammatory cytokines and myofibroblast features in fBMFs, and could serve as a promising and natural antifibrosis agent.</jats:p>
SDGs

[SDGs]SDG3

Publisher
Wiley
Type
journal-article
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