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Two Small Molecules Block Oral Epithelial Cell Invasion by Porphyromons gingivalis.
Ho, Meng-Hsuan; Huang, Li; Goodwin, J Shawn; Dong, Xinhong; Chen, Chin-Ho; Xie, Hua.
Afiliação
  • Ho MH; School of Dentistry, Meharry Medical College, Nashville, Tennessee, United States of America.
  • Huang L; Department of Surgery, Duke University Medical Center, Durham, North Carolina, United States of America.
  • Goodwin JS; Department of Biochemistry and Cancer Biology, Meharry Medical College, Nashville, Tennessee, United States of America.
  • Dong X; Department of Microbiology, Meharry Medical College, Nashville, Tennessee, United States of America.
  • Chen CH; Department of Surgery, Duke University Medical Center, Durham, North Carolina, United States of America.
  • Xie H; School of Dentistry, Meharry Medical College, Nashville, Tennessee, United States of America.
PLoS One ; 11(2): e0149618, 2016.
Article em En | MEDLINE | ID: mdl-26894834
Porphyromonas gingivalis is a keystone pathogen of periodontitis. One of its bacterial characteristics is the ability to invade various host cells, including nonphagocytic epithelial cells and fibroblasts, which is known to facilitate P. gingivalis adaptation and survival in the gingival environment. In this study, we investigated two small compounds, Alop1 and dynasore, for their role in inhibition of P. gingivalis invasion. Using confocal microscopy, we showed that these two compounds significantly reduced invasion of P. gingivalis and its outer membrane vesicles into human oral keratinocytes in a dose-dependent manner. The inhibitory effects of dynasore, a dynamin inhibitor, on the bacterial entry is consistent with the notion that P. gingivalis invasion is mediated by a clathrin-mediated endocytic machinery. We also observed that microtubule arrangement, but not actin, was altered in the host cells treated with Alop1 or dynasore, suggesting an involvement of microtubule in this inhibitory activity. This work provides an opportunity to develop compounds against P. gingivalis infection.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article