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Stimulation of cells derived from nifedipine-induced gingival overgrowth with porphyromonas gingivalis, lipopolysaccharide, and interleukin-1β

  • H. K. Lu
  • , H. P. Chou
  • , C. L. Li
  • , M. Y. Wang
  • , L. F. Wang*
  • *此作品的通信作者
  • Taipei Medical University
  • National Taiwan University

研究成果: 期刊稿件文章同行評審

13 引文 斯高帕斯(Scopus)

摘要

The purpose of this study was to clarify the main contributory factor of nifedipine-induced gingival overgrowth either by Porphyromonas gingivalis lipopolysaccharide (Pg-LPS) or interleukin-1 beta (IL-1β). Human gingival fibroblasts from healthy tissues and nifedipine-induced gingival overgrowth tissues were stimulated with nifedipine, IL-1β Escherichia coli lipopolysaccharide (Ec-LPS), and Pg-LPS, and the gene expressions were analyzed by RT-PCR. Analysis of the data showed no strong evidence of a synergistic effect of nifedipine and Pg-LPS on IL-6, connective tissue growth factor (CTGF), and type 1 collagen gene expression of either healthy cells or nifedipine-induced gingival overgrowth cells. Among the three stimulants - IL-1β, Pg-LPS, and Ec-LPS - androgen receptor and IL-6 gene expressions in both the healthy and nifedipine-induced gingival overgrowth groups were strongly up-regulated by the presence of IL-1β only. Furthermore, the responses to IL-1β in the nifedipine-induced gingival overgrowth group were stronger than those of the healthy group. It can be concluded that IL-1β is an important mediator responsible for the higher IL-6 and androgen receptor expression of nifedipine-induced gingival overgrowth cells.

原文英語
頁(從 - 到)1100-1104
頁數5
期刊Journal of Dental Research
86
發行號11
DOIs
出版狀態已出版 - 11 2007
對外發佈

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