Evidence map›Paper›PMID 34497312›Full record

ArticleScientific reports2021

Carbamylation of elastic fibers is a molecular substratum of aortic stiffness.

Manon Doué, Anaïs Okwieka, Alexandre Berquand, Laëtitia Gorisse, Pascal Maurice, Frédéric Velard, Christine Terryn, Michaël Molinari, Laurent Duca, Christine Piétrement and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 8% 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, 23 citations in OpenAlex.

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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

12 authors at 5 institutions in 1 country.

Manon DouéLaboratoire de Biochimie Médicale et Biologie Moléculaire, CNRS/URCA UMR N° 7369 MEDyC Matrice Extracellulaire et Dynamique Cellulaire, Team 2 "Matrix Aging and Vascular Remodeling", Faculté de Médecine, University of Reims Champagne-Ardenne, 51 Rue Cognacq-Jay, 51095, Reims, France.
Anaïs OkwiekaLaboratoire de Biochimie Médicale et Biologie Moléculaire, CNRS/URCA UMR N° 7369 MEDyC Matrice Extracellulaire et Dynamique Cellulaire, Team 2 "Matrix Aging and Vascular Remodeling", Faculté de Médecine, University of Reims Champagne-Ardenne, 51 Rue Cognacq-Jay, 51095, Reims, France.
Alexandre BerquandLRN EA 4682 Laboratoire de Recherche en Nanosciences and NanoMat' Platform, University of Reims Champagne-Ardenne, Reims, France.
Laëtitia GorisseLaboratoire de Biochimie Médicale et Biologie Moléculaire, CNRS/URCA UMR N° 7369 MEDyC Matrice Extracellulaire et Dynamique Cellulaire, Team 2 "Matrix Aging and Vascular Remodeling", Faculté de Médecine, University of Reims Champagne-Ardenne, 51 Rue Cognacq-Jay, 51095, Reims, France.
Pascal MauriceLaboratoire de Biochimie Médicale et Biologie Moléculaire, CNRS/URCA UMR N° 7369 MEDyC Matrice Extracellulaire et Dynamique Cellulaire, Team 2 "Matrix Aging and Vascular Remodeling", Faculté de Médecine, University of Reims Champagne-Ardenne, 51 Rue Cognacq-Jay, 51095, Reims, France.
Frédéric VelardBIOS EA 4691 Biomatériaux et Inflammation en site osseux, University of Reims Champagne-Ardenne, Reims, France.
Christine TerrynPICT Platform, University of Reims Champagne-Ardenne, Reims, France.
Michaël MolinariIPB, CNRS UMR N°5248 CBMN Institute of Chemistry and Biology of Membranes and Nanoobjects, University of Bordeaux, Bordeaux, France.
Laurent DucaLaboratoire de Biochimie Médicale et Biologie Moléculaire, CNRS/URCA UMR N° 7369 MEDyC Matrice Extracellulaire et Dynamique Cellulaire, Team 2 "Matrix Aging and Vascular Remodeling", Faculté de Médecine, University of Reims Champagne-Ardenne, 51 Rue Cognacq-Jay, 51095, Reims, France.
Christine PiétrementLaboratoire de Biochimie Médicale et Biologie Moléculaire, CNRS/URCA UMR N° 7369 MEDyC Matrice Extracellulaire et Dynamique Cellulaire, Team 2 "Matrix Aging and Vascular Remodeling", Faculté de Médecine, University of Reims Champagne-Ardenne, 51 Rue Cognacq-Jay, 51095, Reims, France.
Philippe GilleryLaboratoire de Biochimie Médicale et Biologie Moléculaire, CNRS/URCA UMR N° 7369 MEDyC Matrice Extracellulaire et Dynamique Cellulaire, Team 2 "Matrix Aging and Vascular Remodeling", Faculté de Médecine, University of Reims Champagne-Ardenne, 51 Rue Cognacq-Jay, 51095, Reims, France.
Stéphane JaissonLaboratoire de Biochimie Médicale et Biologie Moléculaire, CNRS/URCA UMR N° 7369 MEDyC Matrice Extracellulaire et Dynamique Cellulaire, Team 2 "Matrix Aging and Vascular Remodeling", Faculté de Médecine, University of Reims Champagne-Ardenne, 51 Rue Cognacq-Jay, 51095, Reims, France. sjaisson@chu-reims.fr.
Centre Hospitalier Universitaire de Reims · FRBiomatériaux et Bioingénierie · FRChimie et Biologie des Membranes et des Nanoobjects · FRLaboratoire de Recherche en NanosciencesUniversité de Reims Champagne-Ardenne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Because of their long lifespan, matrix proteins of the vascular wall, such as elastin, are subjected to molecular aging characterized by non-enzymatic post-translational modifications, like carbamylation which results from the binding of cyanate (mainly derived from the dissociation of urea) to protein amino groups. While several studies have demonstrated a relationship between increased plasma concentrations of carbamylated proteins and the development of cardiovascular diseases, molecular mechanisms explaining the involvement of protein carbamylation in these pathological contexts remain to be fully elucidated. The aim of this work was to determine whether vascular elastic fibers could be carbamylated, and if so, what impact this phenomenon would have on the mechanical properties of the vascular wall. Our experiments showed that vascular elastin was carbamylated in vivo. Fiber morphology was unchanged after in vitro carbamylation, as well as its sensitivity to elastase degradation. In mice fed with cyanate-supplemented water in order to increase protein carbamylation within the aortic wall, an increased stiffness in elastic fibers was evidenced by atomic force microscopy, whereas no fragmentation of elastic fiber was observed. In addition, this increased stiffness was also associated with an increase in aortic pulse wave velocity in ApoE

Indexed as

AnimalsAortaCattleCyanatesElastic TissueElastinMiceProtein CarbamylationVascular StiffnessCyanatesElastinsodium cyanate

Identifiers

PMID34497312
PMCPMC8426361
OpenAlexW3197919949

What OpenQuestion holds

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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.