Literature DB >> 12182902

Ferritin induction protects cortical astrocytes from heme-mediated oxidative injury.

R F Regan1, N Kumar, F Gao, Y Guo.   

Abstract

Hemin is released from hemoglobin after CNS hemorrhage and may contribute to its cytotoxic effect. In a prior study, we demonstrated that heme oxygenase-1 induction protected murine cortical astrocytes from hemoglobin toxicity. Since heme metabolism releases iron, this observation suggested that these cells are able to effectively sequester and detoxify free iron. In this study, we tested the hypotheses that astrocytes increased ferritin synthesis after exposure to heme-bound iron, and that this induction protected cells from subsequent exposure to toxic concentrations of hemin. Incubation with low micromolar concentrations of hemin, hemoglobin, or ferrous sulfate increased ferritin expression, as detected on immunoblots stained with a polyclonal antibody that was raised against horse spleen ferritin. Time course studies demonstrated an increase in ferritin levels within 2 h. Weak and scattered cellular staining was detected by immunohistochemistry in control, untreated cultures, while diffuse immunoreactivity was observed in cultures exposed to heme-bound iron. An enhanced ferritin band was detected on immunoblots from cultures that were treated with purified apoferritin, consistent with astrocytic ferritin uptake. Immunoreactivity after apoferritin treatment was not altered by concomitant treatment with cycloheximide. Pretreatment with apoferritin protected astrocytes from hemin toxicity in a concentration-dependent fashion between 1 and 4 mg/ml. At the highest concentration, cell death due to a 6-h exposure to 30 microM hemin was decreased by about 85%. A protective effect was also produced by induction of endogenous ferritin with nontoxic concentrations of ferrous sulfate, hemoglobin, or hemin. These results suggest that cortical astrocytes respond to exogenous heme-bound or free iron by rapidly increasing ferritin synthesis. The combined action of heme oxygenase-1 and ferritin may be a primary astrocytic defense against heme-mediated injury. Copyright 2002 IBRO

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Year:  2002        PMID: 12182902     DOI: 10.1016/s0306-4522(02)00243-9

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  21 in total

1.  Astrocyte-specific heme oxygenase-1 hyperexpression attenuates heme-mediated oxidative injury.

Authors:  Luna Benvenisti-Zarom; Raymond F Regan
Journal:  Neurobiol Dis       Date:  2007-03-24       Impact factor: 5.996

Review 2.  Genetics of iron regulation and the possible role of iron in Parkinson's disease.

Authors:  Shannon L Rhodes; Beate Ritz
Journal:  Neurobiol Dis       Date:  2008-07-11       Impact factor: 5.996

Review 3.  Neuroproteomics approaches to decipher neuronal regeneration and degeneration.

Authors:  Faneng Sun; Valeria Cavalli
Journal:  Mol Cell Proteomics       Date:  2009-12-17       Impact factor: 5.911

Review 4.  Targeting the Nrf2-Heme Oxygenase-1 Axis after Intracerebral Hemorrhage.

Authors:  Jing Chen-Roetling; Raymond F Regan
Journal:  Curr Pharm Des       Date:  2017       Impact factor: 3.116

Review 5.  Brain iron toxicity: differential responses of astrocytes, neurons, and endothelial cells.

Authors:  Julie A Gaasch; Paul R Lockman; Werner J Geldenhuys; David D Allen; Cornelis J Van der Schyf
Journal:  Neurochem Res       Date:  2007-04-03       Impact factor: 3.996

6.  Effect of iron chelators on methemoglobin and thrombin preconditioning.

Authors:  Jing Chen-Roetling; Jesse Sinanan; Raymond F Regan
Journal:  Transl Stroke Res       Date:  2012-12       Impact factor: 6.829

7.  Increasing expression of H- or L-ferritin protects cortical astrocytes from hemin toxicity.

Authors:  Zhi Li; Jing Chen-Roetling; Raymond F Regan
Journal:  Free Radic Res       Date:  2009-06

8.  Hemin-mediated regulation of an antioxidant-responsive element of the human ferritin H gene and role of Ref-1 during erythroid differentiation of K562 cells.

Authors:  Kenta Iwasaki; Elizabeth L Mackenzie; Kiros Hailemariam; Kensuke Sakamoto; Yoshiaki Tsuji
Journal:  Mol Cell Biol       Date:  2006-04       Impact factor: 4.272

9.  Haptoglobin increases the vulnerability of CD163-expressing neurons to hemoglobin.

Authors:  Jing Chen-Roetling; Raymond F Regan
Journal:  J Neurochem       Date:  2016-07-22       Impact factor: 5.372

10.  Neurons lacking iron regulatory protein-2 are highly resistant to the toxicity of hemoglobin.

Authors:  Raymond F Regan; Mai Chen; Zhi Li; Xuefeng Zhang; Luna Benvenisti-Zarom; Jing Chen-Roetling
Journal:  Neurobiol Dis       Date:  2008-05-03       Impact factor: 5.996

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