Expression of iron homeostasis proteins in the spinal cord in experimental autoimmune encephalomyelitis and their implications for iron accumulation

Juan G. Zarruk, Jennifer L. Berard, Rosmarini Passos dos Santos, Antje Kroner, Jaekwon Lee, Paolo Arosio, Samuel David

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

Iron accumulation occurs in the CNS in multiple sclerosis (MS) and in experimental autoimmune encephalomyelitis (EAE). However, the mechanisms underlying such iron accumulation are not fully understood. We studied the expression and cellular localization of molecules involved in cellular iron influx, storage, and efflux. This was assessed in two mouse models of EAE: relapsing-remitting (RR-EAE) and chronic (CH-EAE). The expression of molecules involved in iron homeostasis was assessed at the onset, peak, remission/progressive and late stages of the disease. We provide several lines of evidence for iron accumulation in the EAE spinal cord which increases with disease progression and duration, is worse in CH-EAE, and is localized in macrophages and microglia. We also provide evidence that there is a disruption of the iron efflux mechanism in macrophages/microglia that underlie the iron accumulation seen in these cells. Macrophages/microglia also lack expression of the ferroxidases (ceruloplasmin and hephaestin) which have antioxidant effects. In contrast, astrocytes which do not accumulate iron, show robust expression of several iron influx and efflux proteins and the ferroxidase ceruloplasmin which detoxifies ferrous iron. Astrocytes therefore are capable of efficiently recycling iron from sites of EAE lesions likely into the circulation. We also provide evidence of marked dysregulation of mitochondrial function and energy metabolism genes, as well as of NADPH oxidase genes in the EAE spinal cord. This data provides the basis for the selective iron accumulation in macrophage/microglia and further evidence of severe mitochondrial dysfunction in EAE. It may provide insights into processes underling iron accumulation in MS and other neurodegenerative diseases in which iron accumulation occurs.

Original languageEnglish (US)
Pages (from-to)93-107
Number of pages15
JournalNeurobiology of Disease
Volume81
DOIs
StatePublished - Sep 1 2015

Fingerprint

Autoimmune Experimental Encephalomyelitis
Spinal Cord
Homeostasis
Iron
Proteins
Microglia
Macrophages
Ceruloplasmin
Astrocytes
Multiple Sclerosis
NADPH Oxidase
Recycling
Neurodegenerative Diseases
Energy Metabolism
Genes
Disease Progression

Keywords

  • Ceruloplasmin
  • Experimental autoimmune encephalomyelitis
  • Ferroportin
  • Hepcidin
  • Iron
  • Iron efflux
  • Iron influx
  • MS
  • Macrophage
  • Microglia

ASJC Scopus subject areas

  • Neurology

Cite this

Expression of iron homeostasis proteins in the spinal cord in experimental autoimmune encephalomyelitis and their implications for iron accumulation. / Zarruk, Juan G.; Berard, Jennifer L.; Passos dos Santos, Rosmarini; Kroner, Antje; Lee, Jaekwon; Arosio, Paolo; David, Samuel.

In: Neurobiology of Disease, Vol. 81, 01.09.2015, p. 93-107.

Research output: Contribution to journalArticle

Zarruk, Juan G. ; Berard, Jennifer L. ; Passos dos Santos, Rosmarini ; Kroner, Antje ; Lee, Jaekwon ; Arosio, Paolo ; David, Samuel. / Expression of iron homeostasis proteins in the spinal cord in experimental autoimmune encephalomyelitis and their implications for iron accumulation. In: Neurobiology of Disease. 2015 ; Vol. 81. pp. 93-107.
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abstract = "Iron accumulation occurs in the CNS in multiple sclerosis (MS) and in experimental autoimmune encephalomyelitis (EAE). However, the mechanisms underlying such iron accumulation are not fully understood. We studied the expression and cellular localization of molecules involved in cellular iron influx, storage, and efflux. This was assessed in two mouse models of EAE: relapsing-remitting (RR-EAE) and chronic (CH-EAE). The expression of molecules involved in iron homeostasis was assessed at the onset, peak, remission/progressive and late stages of the disease. We provide several lines of evidence for iron accumulation in the EAE spinal cord which increases with disease progression and duration, is worse in CH-EAE, and is localized in macrophages and microglia. We also provide evidence that there is a disruption of the iron efflux mechanism in macrophages/microglia that underlie the iron accumulation seen in these cells. Macrophages/microglia also lack expression of the ferroxidases (ceruloplasmin and hephaestin) which have antioxidant effects. In contrast, astrocytes which do not accumulate iron, show robust expression of several iron influx and efflux proteins and the ferroxidase ceruloplasmin which detoxifies ferrous iron. Astrocytes therefore are capable of efficiently recycling iron from sites of EAE lesions likely into the circulation. We also provide evidence of marked dysregulation of mitochondrial function and energy metabolism genes, as well as of NADPH oxidase genes in the EAE spinal cord. This data provides the basis for the selective iron accumulation in macrophage/microglia and further evidence of severe mitochondrial dysfunction in EAE. It may provide insights into processes underling iron accumulation in MS and other neurodegenerative diseases in which iron accumulation occurs.",
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