HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Dynamic changes in the functional characteristics of the interstitial fibroblast during lung repair.

Abstract
To evaluate the mechanisms involved in the regulation of fibroblast function during the repair of fibrotic lung injury, we isolated lung fibroblasts from adult male Fischer-344 rats before the induction of severe unilateral paraquat lung injury, as well as 1 and 14 days later. Fibroblasts were utilized at an early generation time to avoid senescence. In general, fibroblasts of injured lungs displayed significant increases in proliferative and matrix synthesis properties, with more pronounced increases detected early after the induction of injury. This was true of DNA synthesis, which increased by 3- and 1.4-fold on days 1 and 14, respectively; tyrosine kinase activity, which increased by 4- and 3.5-fold; fibronectin synthesis, 14- and 8-fold, respectively; and glycosaminoglycans synthesis, 4.4- and 3-fold, respectively. The increase in function of fibroblasts isolated from the immediate influence of extrinsic growth factors suggests that fibroblast function during repair may be under intrinsic as well as extrinsic control. In the early phases of repair, intrinsic changes may be more dominant and may result in autoregulation of fibroblast function. In the later phases of repair, despite some reduction in intrinsic fibroblast activation, exposure to extrinsic growth factors may result in maintaining the state of activation and in sustaining the repair process.
AuthorsB A Dubaybo, G J Rubeiz, S E Fligiel
JournalExperimental lung research (Exp Lung Res) Vol. 18 Issue 4 Pg. 461-77 ( 1992) ISSN: 0190-2148 [Print] England
PMID1516567 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Fibronectins
  • Glycosaminoglycans
  • Proteins
  • DNA
  • Protein-Tyrosine Kinases
Topics
  • Animals
  • Autoradiography
  • Cell Division (physiology)
  • Cell Separation
  • Cells, Cultured
  • DNA (biosynthesis)
  • Fibroblasts (cytology, metabolism, ultrastructure)
  • Fibronectins (analysis)
  • Glycosaminoglycans (biosynthesis)
  • Male
  • Phosphorylation
  • Protein-Tyrosine Kinases (metabolism)
  • Proteins (analysis)
  • Pulmonary Fibrosis (pathology)
  • Rats
  • Rats, Inbred F344
  • Time Factors

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: