Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
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Target Concepts:
Gene/Protein
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Query: UMLS:C0037116 (
silicosis
)
1,822
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Transforming growth factor-alpha
(
TGF-alpha
) a cytokine having potent mitogenic activity for epithelial and mesenchymal cells, may play a role in the lung remodeling of
silicosis
. Lung macrophages are among the major cells producing
TGF-alpha
in a lung tissue. A pivotal event in the cascade of pathologic events leading to pulmonary
silicosis
is the interaction between inhaled silica and macrophages.
TGF-alpha
may be critical in directing the proliferation of type II pneumocytes that characterize
silicosis
. An inhalation model of brief exposure of pathogen-restricted male rats to 25 mg/M3 cristobalite, a highly reactive form of silicon dioxide was used to study experimental
silicosis
. This model is characterized by a rapid, intense, and sustained increase in macrophages, neutrophils, and lymphocytes in both alveolar and interstitial compartments of the lung.
TGF-alpha
was measured in an A431 cell proliferation assay made specific with the use of anti-
TGF-alpha
neutralizing antiserum in epithelial lining fluid (ELF) and conditioned media harvested from cultured alveolar and interstitial macrophages. Soluble
TGF-alpha
levels found in ELF were slightly elevated above control values during the exposure period, then increased 5-fold during the 20 weeks after the 8-day exposure period. Secretion of
TGF-alpha
by macrophages was elevated during exposure to cristobalite but then fell during the early post exposure period. Marked elevations in
TGF-alpha
secretion from both interstitial and alveolar macrophages (10- and 12-fold, respectively) occurred 8-16 weeks after cessation of exposure.(ABSTRACT TRUNCATED AT 250 WORDS)
...
PMID:Patterns of secretion of transforming growth factor-alpha (TGF-alpha) in experimental silicosis. Acute and subacute effects of cristobalite exposure in the rat. 824 Sep 39