Evidence map›Paper›PMID 26356734›Full record

ArticlePloS one2015

Gene Expression and MicroRNA Expression Analysis in Small Arteries of Spontaneously Hypertensive Rats. Evidence for ER Stress.

Teresa Palao, Karl Swärd, Aldo Jongejan, Perry D Moerland, Judith de Vos, Angela van Weert, Silvia M Arribas, Gergely Groma, Ed vanBavel, Erik N T P Bakker

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Review
  3. Early Programming of Adult Systemic Essential Hypertension.International journal of molecular sciences · 2020
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
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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

10 authors at 3 institutions in 3 countries.

Teresa PalaoDepartment of Biomedical Engineering and Physics, Academic Medical Center, Amsterdam, The Netherlands.
Karl SwärdDepartment of Experimental Medical Science, Lund University, Lund, Sweden.
Aldo JongejanBioinformatics Laboratory, Academic Medical Center, Amsterdam, The Netherlands.
Perry D MoerlandBioinformatics Laboratory, Academic Medical Center, Amsterdam, The Netherlands.
Judith de VosDepartment of Biomedical Engineering and Physics, Academic Medical Center, Amsterdam, The Netherlands.
Angela van WeertDepartment of Biomedical Engineering and Physics, Academic Medical Center, Amsterdam, The Netherlands.
Silvia M ArribasDepartamento de Fisiología, Facultad de Medicina, Universidad Autónoma de Madrid, Madrid, Spain.
Gergely GromaDepartment of Biomedical Engineering and Physics, Academic Medical Center, Amsterdam, The Netherlands.
Ed vanBavelDepartment of Biomedical Engineering and Physics, Academic Medical Center, Amsterdam, The Netherlands.
Erik N T P BakkerDepartment of Biomedical Engineering and Physics, Academic Medical Center, Amsterdam, The Netherlands.
Academic Medical Center · NLLund University · SEUniversidad Autónoma de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small arteries are known to develop functional and structural alterations in hypertension. However, the mechanisms of this remodeling are not fully understood. We hypothesized that altered gene expression is associated with the development of hypertension in mesenteric arteries of spontaneously hypertensive rats (SHR). Three sublines of SHR and normotensive Wistar Kyoto rats (WKY) were studied at 6 weeks and 5 months of age. MiRNA and mRNA microarray experiments were performed and analyzed with bioinformatical tools, including Ingenuity Pathway Analysis (IPA). Principal component analysis showed a clear separation in both miRNA and mRNA expression levels between both ages studied, demonstrating strong age-related changes in expression. At the miRNA level, IPA identified differences between SHR and WKY related to metabolic diseases, cellular growth, and proliferation. The mRNAs differentially expressed between SHR and WKY were related to metabolism, cellular movement and proliferation. The most strongly upregulated gene (9.2-fold) was thrombospondin 4 (Thbs4), a protein involved in the endoplasmic reticulum (ER) stress response that activates transcription factor 6α (ATF6α). ATF6α downstream targets were also differentially expressed in SHR vs. WKY. Differential expression of THBS4, the cleaved form of ATF6α, and two of its targets were further confirmed at the protein level by western blot. In summary, these data revealed a number of genes (n = 202) and miRNAs (n = 3) in mesenteric arteries of SHR that had not been related to hypertension previously. The most prominent of these, Thbs4, is related to vascular ER stress that is associated with hypertension.

Indexed as

Gene Expression RegulationAnimalsCluster AnalysisDown-RegulationEndoplasmic Reticulum StressGene Expression ProfilingMaleMesenteric ArteriesMicroRNAsOligonucleotide Array Sequence AnalysisPrincipal Component AnalysisRats, Inbred SHRRats, Inbred WKYReal-Time Polymerase Chain ReactionReproducibility of ResultsRNA, MessengerMicroRNAsRNA, Messengerthrombospondin 4Thrombospondins

Identifiers

PMID26356734
PMCPMC4565692
OpenAlexW2173565230

What OpenQuestion holds

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LicenceCC BY
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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.