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TGF-${\beta}1$으로 자극한 사람중피세포주에서 조직플라스미노겐 활성제가 미치는 영향

The Effect of Tissue Plasminogen Activator on TGF-${\beta}1$ Pre-Treated Human Mesothelial Cell Line

  • 이정림 (건양대학교 의과대학 미생물학교실) ;
  • 전수진 (건양대학교 의과대학 미생물학교실) ;
  • 유영춘 (건양대학교 의과대학 미생물학교실) ;
  • 김지혜 (건양대학교 의과대학 내과학교실) ;
  • 이유미 (건양대학교 의과대학 내과학교실) ;
  • 권선중 (건양대학교 의과대학 내과학교실) ;
  • 손지웅 (건양대학교 의과대학 내과학교실) ;
  • 최유진 (건양대학교 의과대학 내과학교실) ;
  • 나문준 (건양대학교 의과대학 내과학교실)
  • Lee, Jung-Lim (Department of Microbiology, Konyang University College of Medicine) ;
  • Jeon, Soo-Jin (Department of Microbiology, Konyang University College of Medicine) ;
  • Yoo, Young-Choon (Department of Microbiology, Konyang University College of Medicine) ;
  • Kim, Ji-Hye (Department of Internal Medicine, Konyang University College of Medicine) ;
  • Lee, Yu-Mi (Department of Internal Medicine, Konyang University College of Medicine) ;
  • Kwon, Sun-Jung (Department of Internal Medicine, Konyang University College of Medicine) ;
  • Son, Ji-Woong (Department of Internal Medicine, Konyang University College of Medicine) ;
  • Choi, Eu-Gene (Department of Internal Medicine, Konyang University College of Medicine) ;
  • Na, Moon-Jun (Department of Internal Medicine, Konyang University College of Medicine)
  • 투고 : 2011.01.07
  • 심사 : 2011.04.04
  • 발행 : 2011.05.30

초록

Background: In an effort to find alternative therapeutic agents to prevent excessive fibrosis as a sequela to complicated parapneumonic effusion or empyema, we examined the effect of tissue plasminogen activator (tPA) as a fibrinolytic agent combined with talc or transforming growth factor (TGF)-${\beta}1$ in a human pleural mesothelial cell line, MeT-5A. Methods: MeT-5A cells were stimulated with various doses of talc, doxycycline or TGF-${\beta}1$ for 24 h and then were treated with tPA for an additional 24 h. Cell viability was measured by MTT assay. The production of interleukin (IL)-8 and vascular endothelial growth factor (VEGF) in the culture supernatants was measured by ELISA. Real-time PCR was carried out for measurement of type I collagen mRNA. Results: MeT-5A cells treated with talc showed a dose-dependent increase in production of IL-8. Talc also increased production of type I collagen mRNA at low doses, but talc did not influence the induction of VEGF. Addition of tPA to talc-stimulated cells showed further increases in the production of IL-8, but tPA did not influence the production of VEGF or type I collagen mRNA. TGF-${\beta}1$ increased the production of both VEGF and collagen type I mRNA, both of which were effectively inhibited by additional tPA treatment in MeT-5A cells. Conclusion: TGF-${\beta}1$ is a potent inducer of collagen synthesis without induction of IL-8 in MeT-5A cells. Addition of tPA after TGF-${\beta}1$ stimulation inhibited further fibrosis by direct inhibition of collagen mRNA synthesis as well as by inhibition of VEGF production.

키워드

참고문헌

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