Evidence map›Paper›PMID 21499502›Full record

ArticleNeurological research2011

Polyadenylated mRNA staining reveals distinct neuronal phenotypes following endothelin 1, focal brain ischemia, and global brain ischemia/ reperfusion.

Jill T Jamison, Monique K Lewis, Christian W Kreipke, José A Rafols, Donald J DeGracia

Abstract readComparative Study
In one paragraph

Article in Neurological research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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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

2 citing papers in PubMed.

  1. Article
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jill T JamisonDepartment of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Monique K Lewis
Christian W Kreipke
José A Rafols
Donald J DeGracia

Funding

Stress Granules Cause Translation Arrest In Ischemic Vulunerable NeuronsR01NS057167 · NINDS · WAYNE STATE UNIVERSITY · PI DEGRACIA, DONALD J · 2008 to 2012
$1.7M
Molecular Mechanisms of Enhanced Contractility following Traumatic Brain Injury:R01NS064976 · NINDS · WAYNE STATE UNIVERSITY · PI KREIPKE, CHRISTIAN W · 2009 to 2011
$988k
NINDS NIH HHS NS-057167NINDS NIH HHS NS-064976NINDS NIH HHS R01 NS057167NINDS NIH HHS R01 NS064976
6 · The paper itself

Abstract

objectivesMost work on ischemia-induced neuronal death has revolved around the relative contributions of necrosis and apoptosis, but this work has not accounted for the role of ischemia-induced stress responses. An expanded view recognizes a competition between ischemia-induced damage mechanisms and stress responses in the genesis of ischemia-induced neuronal death. An important marker of post-ischemic stress responses is inhibition of neuronal protein synthesis, a morphological correlate of which is the compartmentalization of mRNA away from ribosomes in the form of cytoplasmic mRNA granules.

methodsHere we assessed the generality of this mRNA granule response following either 10 or 15 minutes global brain ischemia and 1 hour reperfusion, 4 hours focal cerebral ischemia alone, and endothelin 1 intraventricular injection.

resultsBoth global and focal ischemia led to prominent neuronal cytoplasmic mRNA granule formation in layer II cortical neurons. In addition, we report here new post-ischemic cellular phenotypes characterized by the loss of nuclear polyadenylated mRNA staining in cortical neurons following endothelin 1 treatment and 15 minutes global ischemia. Both mRNA granulation and loss of nuclear mRNAs occurred in non-shrunken post-ischemic neurons. DISCUSSION: Where cytoplasmic mRNA granules generally appear to mark a protective response in surviving cells, loss of nuclear mRNAs may mark cellular damage leading to cell atrophy/death. Hence, staining for total mRNA may reveal facets of the competition between stress responses and damage mechanisms at early stages in post-ischemic neurons.

Indexed as

PhenotypeStress, PhysiologicalAnimalsBrain IschemiaDisease Models, AnimalEndothelin-1MaleNerve DegenerationRatsRats, Long-EvansReperfusion InjuryRNA, MessengerEndothelin-1RNA, Messengerbrain ischemia and reperfusionendothelin 1mRNA granulesprotein synthesis inhibition

Identifiers

PMID21499502
PMCPMC3074580

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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.