Post-transcriptional regulation of plasminogen activator inhibitor-1 by intracellular iron in cultured human lung fibroblasts--interaction of an 81-kDa nuclear protein with the 3'-UTR

J Thromb Haemost. 2005 May;3(5):1001-8. doi: 10.1111/j.1538-7836.2005.01272.x.

Abstract

The proteinase inhibitor, type-1 plasminogen activator inhibitor (PAI-1), is a major regulator of the plasminogen activator system involved in plasmin formation and fibrinolysis. The present study explores the effects of intracellular iron on the expression of PAI-1 and associated cell-surface plasmin activity in human lung fibroblasts; and reports the presence of a novel iron-responsive protein. ELISA revealed a dose-dependent increase in PAI-1 antigen levels expressed in the conditioned medium of cells treated with deferoxamine, in the three cell lines studied. A concomitant increase in mRNA levels was also observed by Northern analyses. Presaturation with ferric citrate quenched the effect of deferoxamine. Experiments with transcription and translation inhibitors on TIG 3-20 cells demonstrated that intracellular iron modulated PAI-1 expression at the post-transcriptional level with the requirement of de-novo protein synthesis. Electrophoretic mobility shift assay and UV crosslinking assays revealed the presence of an approximately 81-kDa nuclear protein that interacted with the 3'-UTR of PAI-1 mRNA in an iron-sensitive manner. Finally, we demonstrated that the increased PAI-1 is functional in suppressing cell-surface plasmin activity, a process that can affect wound healing and tissue remodeling.

MeSH terms

  • 3' Untranslated Regions
  • Antigens / chemistry
  • Blotting, Northern
  • Cell Membrane / metabolism
  • Cell Nucleus / metabolism
  • Cells, Cultured
  • Cross-Linking Reagents / pharmacology
  • Culture Media, Conditioned / pharmacology
  • Cycloheximide / pharmacology
  • Cytoplasm / metabolism
  • Deferoxamine / pharmacology
  • Dose-Response Relationship, Drug
  • Enzyme-Linked Immunosorbent Assay
  • Ferric Compounds / pharmacology
  • Fibrinolysin / metabolism
  • Fibroblasts / cytology*
  • Fibroblasts / metabolism
  • Humans
  • Iron / metabolism
  • Lung / cytology*
  • Plasmids / metabolism
  • Plasminogen Activator Inhibitor 1 / genetics*
  • Plasminogen Activator Inhibitor 1 / metabolism*
  • Protein Biosynthesis
  • RNA Processing, Post-Transcriptional*
  • RNA, Messenger / metabolism
  • Time Factors
  • Transcription, Genetic
  • Ultraviolet Rays
  • Wound Healing

Substances

  • 3' Untranslated Regions
  • Antigens
  • Cross-Linking Reagents
  • Culture Media, Conditioned
  • Ferric Compounds
  • Plasminogen Activator Inhibitor 1
  • RNA, Messenger
  • ferric citrate
  • Cycloheximide
  • Iron
  • Fibrinolysin
  • Deferoxamine