Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0040586 (
tracheobronchitis
)
449
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Hepatocyte growth factor
(
HGF
) promotes lung epithelial repair after injury. Because prior studies established that human neutrophil proteases inactivate
HGF
in vitro, we predicted that
HGF
levels decrease in lungs infiltrated with neutrophils and that injury is less severe in lungs lacking
HGF
-inactivating proteases. After establishing that mouse neutrophil elastase cleaves mouse
HGF
in vitro, we tested our predictions in vivo by examining lung pathology and
HGF
in mice infected with Mycoplasma pulmonis, which causes neutrophilic
tracheobronchitis
and pneumonia. Unexpectedly, pneumonia severity was similar in wild type and dipeptidylpeptidase I-deficient (Dppi-/-) mice lacking neutrophil serine protease activity. To assess how this finding related to our prediction that Dppi-activated proteases regulate
HGF
levels, we measured
HGF
in serum, bronchoalveolar lavage fluid, and lung tissue from Dppi(+/+) and Dppi(-/-) mice. Contrary to prediction,
HGF
levels were higher in lavage fluid from infected mice. However, serum and tissue concentrations were not different in infected and uninfected mice, and
HGF
lung transcript levels did not change. Increased
HGF
correlated with increased albumin in lavage fluid from infected mice, and immunostaining failed to detect increased lung tissue expression of
HGF
in infected mice. These findings are consistent with trans-alveolar flux rather than local production as the source of increased
HGF
in lavage fluid. However, levels of intact
HGF
from infected mice, normalized for albumin concentration, were two-fold higher in Dppi(-/-) versus Dppi(+/+) lavage fluid, suggesting regulation by Dppi-activated proteases. Consistent with the presence of active
HGF
, increased expression of activated receptor c-Met was observed in infected tissues. These data suggest that
HGF
entering alveoli from the bloodstream during pneumonia compensates for destruction by Dppi-activated inflammatory proteases to allow
HGF
to contribute to epithelial repair.
...
PMID:Regulation of hepatocyte growth factor in mice with pneumonia by peptidases and trans-alveolar flux. 2593 94