Evidence map›Paper›PMID 32143215›Full record

ArticlePloS one2020

Optimisation of cell and ex vivo culture conditions to study vascular calcification.

Nathalie Gayrard, Karen Muyor, Cécile Notarnicola, Flore Duranton, Bernard Jover, Àngel Argilés

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. 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
1.4field-weighted citation impact, top 19% 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, 12 citations in OpenAlex.

  1. Review
  2. Article
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  9. Review
  10. Research Models for Studying Vascular Calcification.International journal of molecular sciences · 2020
    Review
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

6 authors at 2 institutions in 1 country.

Nathalie GayrardRD - Néphrologie 2, rue de Mûriers, Montpellier, France.ORCID 0000-0001-8283-8429
Karen MuyorRD - Néphrologie 2, rue de Mûriers, Montpellier, France.
Cécile NotarnicolaPhyMedExp (Physiologie et Médecine Expérimentale Cœur Muscles), INSERM-CNRS-Université Montpellier, IURC, Montpellier, France.
Flore DurantonRD - Néphrologie 2, rue de Mûriers, Montpellier, France.
Bernard JoverPhyMedExp (Physiologie et Médecine Expérimentale Cœur Muscles), INSERM-CNRS-Université Montpellier, IURC, Montpellier, France.ORCID 0000-0001-5826-5755
Àngel ArgilésRD - Néphrologie 2, rue de Mûriers, Montpellier, France.
Université de Montpellier · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Medial vascular calcification (MVC) is a highly prevalent disease associated with a high risk of severe, potentially lethal, complications. While animal studies may not systematically be circumvented, in vitro systems have been proven useful to study disease physiopathology. In the context of MVC, the absence of a clinically relevant standardized in vitro method prevents the appropriate comparison and overall interpretation of results originating from different experiments. The aim of our study is to establish in vitro models mimicking in vivo vascular calcification and to select the best methods to unravel the mechanisms involved in MVC. Human aortic smooth muscle cells and rat aortic rings were cultured in different conditions. The influence of fetal calf serum (FCS), alkaline phosphatase, phosphate and calcium concentrations in the medium were evaluated. We identified culture conditions, including the herein reported Aorta Calcifying Medium (ACM), which allowed a reproducible and specific medial calcification of aortic explants. Studying cells and aortic explants cultured, the involvement of bone morphogenetic protein 2 (BMP2) pathway, fibrosis and apoptosis processes in in vitro MVC were demonstrated. Expression of osteoblastic markers was also observed suggesting the occurrence of transdifferentiation of smooth muscle cells to osteoblasts in our models. The use of these models will help researchers in the field of vascular calcification to achieve reproducible results and allow result comparison in a more consistent way.

Indexed as

Alkaline PhosphataseAnimalsAortaApoptosisBone Morphogenetic Protein 2CalciumCells, CulturedCell TransdifferentiationHumansMuscle, Smooth, VascularMyocytes, Smooth MuscleOsteoblastsPhosphatesRatsRats, WistarSignal TransductionAlkaline PhosphataseBone Morphogenetic Protein 2CalciumPhosphates

Identifiers

PMID32143215
PMCPMC7060075
OpenAlexW3009371342

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.