Intra-airway administration of small interfering RNA targeting plasminogen activator inhibitor-1 attenuates allergic asthma in mice

Am J Physiol Lung Cell Mol Physiol. 2011 Dec;301(6):L908-16. doi: 10.1152/ajplung.00115.2011. Epub 2011 Sep 16.

Abstract

Recent studies suggest that plasminogen activator inhibitor-1 (PAI-1), a major inhibitor of the fibrinolytic system, may promote the development of asthma. To further investigate the significance of PAI-1 in the pathogenesis of asthma and determine the possibility that PAI-1 could be a therapeutic target for asthma, this study was conducted. First, PAI-1 levels in induced sputum (IS) from asthmatic subjects and healthy controls were measured. In asthmatic subjects, IS PAI-1 levels were elevated, compared with that of healthy controls, and were significantly higher in patients with long-duration asthma compared with short-duration asthma. PAI-1 levels were also found to correlate with IS transforming growth factor-β levels. Then, acute and chronic asthma models induced by ovalbumin were established in PAI-1-deficient mice and wild-type mice that received intra-airway administrations of small interfering RNA against PAI-1 (PAI-1-siRNA). We could demonstrate that eosinophilic airway inflammation and airway hyperresponsiveness were reduced in an acute asthma model, and airway remodeling was suppressed in a chronic asthma model in both PAI-1-deficient mice and wild-type mice that received intra-airway administration of PAI-1-siRNA. These results indicate that PAI-1 is strongly involved in the pathogenesis of asthma, and intra-airway administration of PAI-1-siRNA may be able to become a new therapeutic approach for asthma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Airway Remodeling / genetics
  • Animals
  • Asthma / pathology
  • Asthma / prevention & control*
  • Bronchitis / prevention & control
  • Bronchoalveolar Lavage Fluid / chemistry
  • Drug Evaluation, Preclinical
  • Female
  • Hepatocyte Growth Factor / metabolism
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Molecular Targeted Therapy
  • Ovalbumin
  • Plasminogen Activator Inhibitor 1 / genetics*
  • Plasminogen Activator Inhibitor 1 / metabolism
  • Pulmonary Eosinophilia / pathology
  • Pulmonary Eosinophilia / prevention & control
  • RNA Interference*
  • RNA, Small Interfering / administration & dosage
  • RNA, Small Interfering / therapeutic use*
  • Sputum / metabolism

Substances

  • HGF protein, mouse
  • Plasminogen Activator Inhibitor 1
  • RNA, Small Interfering
  • Hepatocyte Growth Factor
  • Ovalbumin