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Effect of exogenous hepatocyte growth factor on vocal fold fibroblasts.

AbstractOBJECTIVES:
We have previously demonstrated the therapeutic potential of hepatocyte growth factor (HGF) in the treatment of vocal fold scarring, although how exogenous HGF affects gene expression of endogenous HGF or extracellular matrix components in the vocal fold fibroblasts remains unclear. In this in vitro study, we aimed to clarify this aspect in order to better understand the effects of HGF on the vocal folds.
METHODS:
Fibroblasts were obtained from the lamina propria of the vocal folds of 5 Sprague-Dawley rats and were cultured with HGF at concentrations of 100, 10, 1, and 0 ng/mL. The cells were collected on days 1, 3, and 7, and the expression of endogenous HGF, its receptor c-Met, transforming growth factor-beta1 (TGF-beta1), procollagen types I and III, and hyaluronic acid synthase (HAS)-1 and HAS-2 messenger RNAs (mRNAs) was examined by real-time reverse transcription-polymerase chain reaction.
RESULTS:
The expression of endogenous HGF and HAS-1 mRNAs increased significantly when exogenous HGF was administered at a concentration of 1 ng/mL. On day 1, the expression of TGF-beta1 and HAS-2 mRNAs increased significantly in response to 1 ng/mL HGF.
CONCLUSIONS:
Exogenous HGF triggered the up-regulation of endogenous HGF, TGF-beta1, HAS-1, and HAS-2 mRNAs in vocal fold fibroblasts.
AuthorsYo Kishimoto, Shigeru Hirano, Atsushi Suehiro, Ichiro Tateya, Shin-ichi Kanemaru, Tatsuo Nakamura, Juichi Ito
JournalThe Annals of otology, rhinology, and laryngology (Ann Otol Rhinol Laryngol) Vol. 118 Issue 8 Pg. 606-11 (Aug 2009) ISSN: 0003-4894 [Print] United States
PMID19746761 (Publication Type: Journal Article)
Chemical References
  • HGF protein, human
  • Procollagen
  • RNA, Messenger
  • Recombinant Proteins
  • Transforming Growth Factor beta1
  • Hepatocyte Growth Factor
  • Glucuronosyltransferase
  • Has2 protein, rat
  • Hyaluronan Synthases
  • Proto-Oncogene Proteins c-met
Topics
  • Animals
  • Cell Culture Techniques
  • Fibroblasts (drug effects, metabolism)
  • Glucuronosyltransferase (genetics, metabolism)
  • Hepatocyte Growth Factor (metabolism, pharmacology)
  • Hyaluronan Synthases
  • Male
  • Procollagen (genetics, metabolism)
  • Proto-Oncogene Proteins c-met (genetics, metabolism)
  • RNA, Messenger (metabolism)
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins (pharmacology)
  • Transforming Growth Factor beta1 (genetics, metabolism)
  • Vocal Cords (drug effects, metabolism, pathology)

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