Evidence map›Paper›PMID 29925894›Full record

ArticleScientific reports2018

Stem cell properties of peripheral blood endothelial progenitors are stimulated by soluble CD146 via miR-21: potential use in autologous cell therapy.

Amel Essaadi, Marie Nollet, Anaïs Moyon, Jimmy Stalin, Stéphanie Simoncini, Laure Balasse, Alexandrine Bertaud, Richard Bachelier, Aurélie S Leroyer, Gabrielle Sarlon and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Review
  2. Review
  3. Target and Cell Therapy for Atherosclerosis and CVD.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. 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

14 authors.

Amel EssaadiAix Marseille Univ, INSERM 1263, INRA 1260, C2VN, Marseille, France.
Marie NolletAix Marseille Univ, INSERM 1263, INRA 1260, C2VN, Marseille, France.
Anaïs MoyonAix Marseille Univ, INSERM 1263, INRA 1260, C2VN, Marseille, France.
Jimmy StalinAix Marseille Univ, INSERM 1263, INRA 1260, C2VN, Marseille, France.
Stéphanie SimonciniAix Marseille Univ, INSERM 1263, INRA 1260, C2VN, Marseille, France.
Laure BalasseCERIMED (European Center of Research in Medical Imaging), Aix-Marseille University, Marseille, France.
Alexandrine BertaudAix Marseille Univ, INSERM 1263, INRA 1260, C2VN, Marseille, France.
Richard BachelierAix Marseille Univ, INSERM 1263, INRA 1260, C2VN, Marseille, France.
Aurélie S LeroyerAix Marseille Univ, INSERM 1263, INRA 1260, C2VN, Marseille, France.
Gabrielle SarlonService of Vascular Surgery, La Timone Hospital, Marseille, France.
Benjamin GuilletAix Marseille Univ, INSERM 1263, INRA 1260, C2VN, Marseille, France.
Françoise Dignat-GeorgeAix Marseille Univ, INSERM 1263, INRA 1260, C2VN, Marseille, France.
Nathalie BardinAix Marseille Univ, INSERM 1263, INRA 1260, C2VN, Marseille, France.
Marcel Blot-ChabaudAix Marseille Univ, INSERM 1263, INRA 1260, C2VN, Marseille, France. marcel.blot-chabaud@laposte.net.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell-based therapies constitute a real hope for the treatment of ischaemic diseases. One of the sources of endothelial progenitors for autologous cell therapy is Endothelial Colony Forming Cells (ECFC) that can be isolated from peripheral blood. However, their use is limited by their low number in the bloodstream and the loss of their stem cell phenotype associated with the acquisition of a senescent phenotype in culture. We hypothesized that adding soluble CD146, a novel endothelial growth factor with angiogenic properties, during the isolation and growth procedures could improve their number and therapeutic potential. Soluble CD146 increased the number of isolated peripheral blood ECFC colonies and lowered their onset time. It prevented cellular senescence, induced a partial mesenchymal phenotype and maintained a stem cell phenotype by stimulating the expression of embryonic transcription factors. These different effects were mediated through the induction of mature miR-21. When injected in an animal model of hindlimb ischaemia, sCD146-primed ECFC isolated from 40 ml of blood from patients with peripheral arterial disease were able to generate new blood vessels and restore blood flow. Treatment with sCD146 could thus constitute a promising strategy to improve the use of autologous cells for the treatment of ischaemic diseases.

Indexed as

AdolescentAdultAnimalsBlotting, WesternCD146 AntigenCell- and Tissue-Based TherapyCell ProliferationEndothelial CellsFlow CytometryHindlimbHumansIschemiaMaleMiceMice, NudeMicroRNAsCD146 AntigenMicroRNAsMIRN21 microRNA, human

Identifiers

PMID29925894
PMCPMC6010456

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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.