Evidence map›Paper›PMID 27328880›Full record

ArticleCardiovascular research2016

The angiotensin II type 2 receptor activates flow-mediated outward remodelling through T cells-dependent interleukin-17 production.

Antoine Caillon, Céline Grenier, Linda Grimaud, Emilie Vessieres, Anne-Laure Guihot, Simon Blanchard, Eric Lelievre, Marie Chabbert, Etienne D Foucher, Pascale Jeannin and 5 more

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Article in Cardiovascular research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Autophagy protein 5 controls flow-dependent endothelial functions.Cellular and molecular life sciences : CMLS · 2023
    Article
  3. The Angiotensin ATPharmacological reviews · 2022
    Review
  4. Article
  5. Dual Role of Thrombospondin-1 in Flow-Induced Remodeling.International journal of molecular sciences · 2021
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. The Impact of Estrogen Receptor in Arterial and Lymphatic Vascular Diseases.International journal of molecular sciences · 2020
    Review
  11. Review
  12. Article
  13. Article
  14. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 1 country.

Antoine CaillonMITOVASC Institute, UMR CNRS 6214, INSERM U1083, Angers University, F-49045 Angers, France UMR CNRS 6299, UMR INSERM 892, Angers University, F-49045 Angers, France.
Céline GrenierMITOVASC Institute, UMR CNRS 6214, INSERM U1083, Angers University, F-49045 Angers, France.
Linda GrimaudMITOVASC Institute, UMR CNRS 6214, INSERM U1083, Angers University, F-49045 Angers, France.
Emilie VessieresMITOVASC Institute, UMR CNRS 6214, INSERM U1083, Angers University, F-49045 Angers, France Cardiovascular Functions In Vitro (CARFI) Facility, Angers University, F-49045 Angers, France.
Anne-Laure GuihotMITOVASC Institute, UMR CNRS 6214, INSERM U1083, Angers University, F-49045 Angers, France.
Simon BlanchardUMR CNRS 6299, UMR INSERM 892, Angers University, F-49045 Angers, France Department of Immunology and Allergology, University Hospital, F-49045 Angers, France.
Eric LelievreMITOVASC Institute, UMR CNRS 6214, INSERM U1083, Angers University, F-49045 Angers, France.
Marie ChabbertMITOVASC Institute, UMR CNRS 6214, INSERM U1083, Angers University, F-49045 Angers, France.
Etienne D FoucherUMR CNRS 6299, UMR INSERM 892, Angers University, F-49045 Angers, France.
Pascale JeanninUMR CNRS 6299, UMR INSERM 892, Angers University, F-49045 Angers, France Department of Immunology and Allergology, University Hospital, F-49045 Angers, France.
Céline BeauvillainUMR CNRS 6299, UMR INSERM 892, Angers University, F-49045 Angers, France Department of Immunology and Allergology, University Hospital, F-49045 Angers, France.
Pierre AbrahamMITOVASC Institute, UMR CNRS 6214, INSERM U1083, Angers University, F-49045 Angers, France Department of Vascular Medicine, University Hospital, F-49045 Angers, France.
Laurent LoufraniMITOVASC Institute, UMR CNRS 6214, INSERM U1083, Angers University, F-49045 Angers, France.
Yves DelnesteUMR CNRS 6299, UMR INSERM 892, Angers University, F-49045 Angers, France Department of Immunology and Allergology, University Hospital, F-49045 Angers, France.
Daniel HenrionMITOVASC Institute, UMR CNRS 6214, INSERM U1083, Angers University, F-49045 Angers, France Cardiovascular Functions In Vitro (CARFI) Facility, Angers University, F-49045 Angers, France Department of Vascular Medicine, University Hospital, F-49045 Angers, France daniel.henrion@inserm.fr.
Centre National de la Recherche Scientifique · FRInserm · FRUniversité d'Angers · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThe angiotensin II type 1 receptor (AT1R) through the activation of immune cells plays a key role in arterial inward remodelling and reduced blood flow in cardiovascular disorders. On the other side, flow (shear stress)-mediated outward remodelling (FMR), involved in collateral arteries growth in ischaemic diseases, allows revascularization. We hypothesized that the type 2 receptor (AT2R), described as opposing the effects of AT1R, could be involved in FMR. METHODS AND

resultsWe studied FMR using a model of ligation of feed arteries supplying collateral pathways in the mouse mesenteric arterial bed in vivo. Seven days after ligation, diameter increased by 30% in high flow (HF) arteries compared with normal flow vessels. FMR was absent in mice lacking AT2R. At Day 2, T lymphocytes expressing AT2R were present preferentially around HF arteries. FMR did not occur in athymic (nude) mice lacking T cells and in mice treated with anti-CD3ε antibodies. AT2R activation induced interleukin-17 production by memory T cells. Treatment of nude mice or AT2R-deficient mice with interleukin-17 restored diameter enlargement in HF arteries. Interleukin-17 increased NO-dependent relaxation and matrix metalloproteinases activity, both important in FMR. Remodelling of feeding arteries in the skin flap model of ischaemia was also absent in AT2R-deficient mice and in anti-interleukin-17-treated mice. Finally, remodelling, absent in 12-month-old mice, was restored by a treatment with the AT2R non-peptidic agonist C21.

conclusionAT2R-dependent interleukin-17 production by T lymphocyte is necessary for collateral artery growth and could represent a new therapeutic target in ischaemic disorders.

Indexed as

Mechanotransduction, CellularSplanchnic CirculationVascular RemodelingAge FactorsAnimalsArterial PressureCD4-Positive T-LymphocytesCollateral CirculationEndothelial CellsGenotypeInterleukin-17IschemiaLigationMacrophagesMesenteric ArteriesMesenteryInterleukin-17Receptor, Angiotensin, Type 2Angiotensin II type 2 receptorBlood flowCollateral artery growthInterleukin-17

Identifiers

PMID27328880
OpenAlexW2467226962

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Registered trials

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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.