Astroglial nitration after postnatal excitotoxic damage: Correlation with nitric oxide sources, cytoskeletal, apoptotic and antioxidant proteins

Laia Acarin, Hugo Peluffo, Luis Barbeito, Bernardo Castellano, Berta González

Research output: Contribution to journalArticleResearchpeer-review

27 Citations (Scopus)

Abstract

Oxygen free radicals and nitric oxide (NO) participate in the pathogenesis of acute central nervous system (CNS) injury by forming peroxynitrite, which promotes oxidative damage and tyrosine nitration. Neuronal nitration is associated with cell death, but little is known of the characteristics and cell fate of nitrated astrocytes. In this study, we have used a postnatal excitotoxic lesion model (intracortical NMDA injection) and our aims were (i) to evaluate the temporal and spatial pattern of astroglial nitration in correlation with the neuropathological process and the sources of NO; and (ii) to establish, if any, the correlation among astrocyte nitration and other events such as expression of cytoskeletal proteins, antioxidant enzymes, and cell death markers to cope with nitration and/or undergo cell death. Our results show that after postnatal excitotoxic damage two distinct waves of nitration were observed in relation to astrocytes. At 24 h post-lesion, early-nitrated astrocytes were found within the neurodegenerating area, coinciding with the time of maximal cell death. These early-nitrated astrocytes are highly ramified protoplasmic cells, showing diffuse glial fibrillary acidic protein (GFAP) content and expressing inducible NOS. At later time-points, when astrogliosis is morphologically evident, nitrated hypertrophied reactive astrocytes are observed in the penumbra and the neurodegenerated area, displaying increased expression of GFAP and vimentin cytoskeletal proteins and of metallothionein I-II and Cu/Zn superoxide dismutase antioxidant proteins. Moreover, despite revealing activated caspase-3, they do not show TUNEL labeling. In summary, we show that nitrated astrocytes in vivo constitute a subpopulation of highly reactive astrocytes which display high resistance towards oxidative stress induced cell death.
Original languageEnglish
Pages (from-to)189-200
JournalJournal of Neurotrauma
Volume22
DOIs
Publication statusPublished - 1 Jan 2005

Keywords

  • Caspase-3
  • Cu/Zn SOD
  • Metallothionein
  • Nitrotyrosine
  • Oxidative stress
  • TUNEL
  • Vimentin

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