Evidence map›Paper›PMID 24160637›Full record

ArticleJournal of neuroinflammation2013

Astrocytes acquire resistance to iron-dependent oxidative stress upon proinflammatory activation.

Romina Macco, Ilaria Pelizzoni, Alessandra Consonni, Ilaria Vitali, Giacomo Giacalone, Filippo Martinelli Boneschi, Franca Codazzi, Fabio Grohovaz, Daniele Zacchetti

Abstract read
In one paragraph

Article in Journal of neuroinflammation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

  1. Article
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  3. Review
  4. Article
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  11. Upregulation of Peroxiredoxin 3 ProtectsOxidative medicine and cellular longevity · 2019
    Article
  12. Article
  13. Article
  14. Persistent Unresolved Inflammation in theMediators of inflammation · 2017
    Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Subclinical inflammatory status in Rett syndrome.Mediators of inflammation · 2014
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Romina Macco
Ilaria Pelizzoni
Alessandra Consonni
Ilaria Vitali
Giacomo Giacalone
Filippo Martinelli Boneschi
Franca Codazzi
Fabio GrohovazDivision of Neuroscience, Dibit, San Raffaele Scientific Institute, via Olgettina 58, 20132, Milano, Italy. grohovaz.fabio@hsr.it.
Daniele Zacchetti

Funding

Telethon GGP10099
6 · The paper itself

Abstract

backgroundAstrocytes respond to local insults within the brain and the spinal cord with important changes in their phenotype. This process, overall known as "activation", is observed upon proinflammatory stimulation and leads astrocytes to acquire either a detrimental phenotype, thereby contributing to the neurodegenerative process, or a protective phenotype, thus supporting neuronal survival. Within the mechanisms responsible for inflammatory neurodegeneration, oxidative stress plays a major role and has recently been recognized to be heavily influenced by changes in cytosolic iron levels. In this work, we investigated how activation affects the competence of astrocytes to handle iron overload and the ensuing oxidative stress.

methodsCultures of pure cortical astrocytes were preincubated with proinflammatory cytokines (interleukin-1β and tumor necrosis factor α) or conditioned medium from lipopolysaccharide-activated microglia to promote activation and then exposed to a protocol of iron overload.

resultsWe demonstrate that activated astrocytes display an efficient protection against iron-mediated oxidative stress and cell death. Based on this evidence, we performed a comprehensive biochemical and molecular analysis, including a transcriptomic approach, to identify the molecular basis of this resistance.

conclusionsWe propose the protective phenotype acquired after activation not to involve the most common astrocytic antioxidant pathway, based on the Nrf2 transcription factor, but to result from a complex change in the expression and activity of several genes involved in the control of cellular redox state.

Indexed as

AnimalsAstrocytesBlotting, WesternIronOxidative StressPhenotypeRatsRats, Sprague-DawleyReverse Transcriptase Polymerase Chain ReactionRNA, Small InterferingTransfectionIronRNA, Small Interfering

Identifiers

PMID24160637
PMCPMC3874684

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.