Proinflammatory cytokines promote glial heme oxygenase-1 expression and mitochondrial iron deposition: implications for multiple sclerosis

J Neurochem. 2001 Jun;77(5):1386-95. doi: 10.1046/j.1471-4159.2001.00354.x.

Abstract

Proinflammatory cytokines, pathological iron deposition, and oxidative stress have been implicated in the pathogenesis of multiple sclerosis (MS) and experimental autoimmune encephalomyelitis (EAE). HO-1 mRNA levels and mitochondrial uptake of [(55)Fe]Cl(3)-derived iron were measured in rat astroglial cultures exposed to interleukin-1beta (IL-1beta) or tumor necrosis factor-alpha (TNF-alpha) alone or in combination with the heme oxygenase-1 (HO-1) inhibitors, tin mesoporphyrin (SnMP) or dexamthasone (DEX), or interferon beta1b (INF-beta). HO-1 expression in astrocytes was evaluated by immunohistochemical staining of spinal cord tissue derived from MS and control subjects. IL-1beta or TNF-alpha promoted sequestration of non-transferrin-derived (55)Fe by astroglial mitochondria. HO-1 inhibitors, mitochondrial permeability transition pore (MTP) blockers and antioxidants significantly attenuated cytokine-related mitochondrial iron sequestration in these cells. IFN-beta decreased HO-1 expression and mitochondrial iron sequestration in IL-1beta- and TNF-alpha-challenged astroglia. The percentage of astrocytes coexpressing HO-1 in affected spinal cord from MS patients (57.3% +/- 12.8%) was significantly greater (p < 0.05) than in normal spinal cord derived from controls subjects (15.4% +/- 8.4%). HO-1 is over-expressed in MS spinal cord astroglia and may promote mitochondrial iron deposition in MS plaques. In MS, IFN-beta may attenuate glial HO-1 gene induction and aberrant mitochondrial iron deposition accruing from exposure to proinflammatory cytokines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Northern
  • Cells, Cultured
  • Chlorides
  • Cytokines / pharmacology*
  • Encephalomyelitis, Autoimmune, Experimental / enzymology
  • Encephalomyelitis, Autoimmune, Experimental / metabolism
  • Female
  • Ferric Compounds / metabolism
  • Heme Oxygenase (Decyclizing) / biosynthesis*
  • Humans
  • Immunohistochemistry
  • Interleukin-1 / pharmacology
  • Iron / metabolism*
  • Iron Radioisotopes
  • Mitochondria / drug effects
  • Mitochondria / metabolism*
  • Multiple Sclerosis / enzymology
  • Multiple Sclerosis / metabolism*
  • Neuroglia / drug effects
  • Neuroglia / enzymology*
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Sprague-Dawley
  • Spinal Cord / metabolism
  • Subcellular Fractions / enzymology
  • Subcellular Fractions / metabolism
  • Transferrin / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Chlorides
  • Cytokines
  • Ferric Compounds
  • Interleukin-1
  • Iron Radioisotopes
  • RNA, Messenger
  • Transferrin
  • Tumor Necrosis Factor-alpha
  • Iron
  • Heme Oxygenase (Decyclizing)
  • ferric chloride