Evidence map›Paper›PMID 23715769›Full record

ArticleMolecular neurobiology2013

Binding and repressive activities of apolipoprotein E3 and E4 isoforms on the human ApoD promoter.

Louis-Charles Levros, Marilyne Labrie, Cyndia Charfi, Eric Rassart

Open access · bronzeAbstract read
In one paragraph

Article in Molecular neurobiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
0.5field-weighted citation impact, top 34% of its field
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

15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Apolipoprotein D as a Potential Biomarker in Neuropsychiatric Disorders.International journal of molecular sciences · 2023
    Review
  6. Apolipoprotein D in Oxidative Stress and Inflammation.Antioxidants (Basel, Switzerland) · 2023
    Review
  7. Article
  8. Studies of ApoDCellular and molecular life sciences : CMLS · 2021
    Article
  9. Apolipoprotein D.Gene · 2020
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Nuclear Localization of Apolipoprotein E4: A New Trick for an Old Protein.International journal of neurology and neurotherapy · 2017
    Article
  15. Direct Transcriptional Effects of Apolipoprotein E.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    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

4 authors at 1 institution in 1 country.

Louis-Charles LevrosLaboratoire de biologie moléculaire, Département des Sciences Biologiques, and BioMed, centre de recherches biomédicales, Université du Québec à Montréal, Montréal, Québec, Canada.
Marilyne Labrie
Cyndia Charfi
Eric Rassart
Université du Québec à Montréal · CA

Funding

Canadian Institutes of Health Research MOP-15677
6 · The paper itself

Abstract

Apolipoprotein D (ApoD) gene expression is increased in several neurological disorders such as Alzheimer's disease (AD) and multiple sclerosis. We previously showed that transgenic mice that overexpress human ApoD show a better resistance against paraquat or OC43 coronavirus-induced neurodegeneration. Here, we identified several nuclear factors from the cortex of control and OC43-infected mice which bind a fragment of the proximal ApoD promoter in vitro. Of interest, we detected apolipoprotein E (ApoE). Human ApoE consists of three isoforms (E2, E3, and E4) with the E4 and E2 alleles representing a greater and a lower risk for developping AD, respectively. Our results show that ApoE is located in the nucleus and on the ApoD promoter in human hepatic and glioblastoma cells lines. Furthermore, overexpression of ApoE3 and ApoE4 isoforms but not ApoE2 significantly inhibited the ApoD promoter activity in U87 cells (E3/E3 genotype) cultured under normal or different stress conditions while ApoE knock-down by siRNA had a converse effect. Consistent with these results, we also demonstrated by ChIP assay that E3 and E4 isoforms, but not E2, bind the ApoD promoter. Moreover, using the Allen Brain Atlas in situ hybridization database, we observed an inverse correlation between ApoD and ApoE mRNA expression during development and in several regions of the mouse brain, notably in the cortex, hippocampus, plexus choroid, and cerebellum. This negative correlation was also observed for cortex layers IV-VI based on a new Transcriptomic Atlas of the Mouse Neocortical Layers. These findings reveal a new function for ApoE by regulating ApoD gene expression.

Indexed as

Promoter Regions, GeneticAnimalsApolipoprotein E3Apolipoprotein E4Apolipoproteins DBase SequenceCell Line, TumorCell NucleusCerebral CortexGene Expression RegulationHumansMass SpectrometryMiceMice, Inbred C57BLMolecular Sequence DataNuclear ProteinsAPOD protein, humanApolipoprotein E3Apolipoprotein E4Apolipoproteins DNuclear ProteinsProtein Isoforms

Identifiers

PMID23715769
PMCPMC7090986
OpenAlexW1967641779

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.