期刊论文详细信息
Tuberculosis and Respiratory Diseases
The Effect of Tissue Plasminogen Activator on TGF-beta1 Pre-Treated Human Mesothelial Cell Line.
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Lee, Junglim1  Jeon, Soo Jin1  Yoo, Young Choon1  Kim, Ji Hye3  Lee, Yu Mi3  Kwon, Sun Jung3  Son, Ji Woong3  Choi, Eugene3  Na, Moon Jun3 
[1] Departments of Microbiology, Konyang University College of Medicine;Departments of Myunggok Research Institute of Medical Science, Konyang University College of Medicine;Departments of Internal Medicine Konyang University College of Medicine;Departments of Konyang University College of Medicine
关键词: Humans;    Mesothelium;    Cell Line;    Tissue Plasminogen Activator;    Transforming Growth Factor;    Collagen;   
DOI  :  10.4046/trd.2011.70.5.405
学科分类:医学(综合)
来源: The Korean Academy of Tuberculosis and Respiratory Diseases
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【 摘 要 】

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)-beta1 in a human pleural mesothelial cell line, MeT-5A. METHODS: MeT-5A cells were stimulated with various doses of talc, doxycycline or TGF-beta1 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-beta1 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-beta1 is a potent inducer of collagen synthesis without induction of IL-8 in MeT-5A cells. Addition of tPA after TGF-beta1 stimulation inhibited further fibrosis by direct inhibition of collagen mRNA synthesis as well as by inhibition of VEGF production.

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