Evidence map›Paper›PMID 30879244›Full record

ArticleStem cell reviews and reports2019

Human Endothelial Colony Forming Cells Express Intracellular CD133 that Modulates their Vasculogenic Properties.

Elisa Rossi, Sonia Poirault-Chassac, Ivan Bieche, Richard Chocron, Anne Schnitzler, Anna Lokajczyk, Pierre Bourdoncle, Blandine Dizier, Nour C Bacha, Nicolas Gendron and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Stem cell reviews and reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 pooled it
2.1field-weighted citation impact, top 13% 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

31 citing papers in PubMed, 2 syntheses or guidelines pooled it, 41 citations in OpenAlex.

  1. Pooled it
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  4. Review
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  7. Review
  8. Pathogens (Basel, Switzerland) · 2024
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  18. Characterization of Endothelial Progenitor Cell: Past, Present, and Future.International journal of molecular sciences · 2022
    Review
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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

14 authors at 3 institutions in 1 country.

Elisa RossiSorbonne Paris Cité, Université Paris Descartes, Paris, France.
Sonia Poirault-ChassacSorbonne Paris Cité, Université Paris Descartes, Paris, France.
Ivan BiecheSorbonne Paris Cité, Université Paris Descartes, Paris, France.
Richard ChocronSorbonne Paris Cité, Université Paris Descartes, Paris, France.
Anne SchnitzlerDepartment of genetics, Pharmacogenomics Unit, Institut Curie, Paris, France.
Anna LokajczykSorbonne Paris Cité, Université Paris Descartes, Paris, France.
Pierre BourdonclePlate-forme IMAG'IC Institut Cochin Inserm U1016-CNRS UMR8104, Université Paris Descartes, Paris, France.
Blandine DizierSorbonne Paris Cité, Université Paris Descartes, Paris, France.
Nour C BachaSorbonne Paris Cité, Université Paris Descartes, Paris, France.
Nicolas GendronSorbonne Paris Cité, Université Paris Descartes, Paris, France.
Adeline BlandinieresSorbonne Paris Cité, Université Paris Descartes, Paris, France.
Coralie L GuerinSorbonne Paris Cité, Université Paris Descartes, Paris, France.
Pascale GaussemSorbonne Paris Cité, Université Paris Descartes, Paris, France.
David M SmadjaSorbonne Paris Cité, Université Paris Descartes, Paris, France. david.smadja@aphp.fr.ORCID 0000-0001-7731-9202
Délégation Paris 5 · FRCentre National de la Recherche Scientifique · FRInstitut Curie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stem cells at the origin of endothelial progenitor cells and in particular endothelial colony forming cells (ECFCs) subtype have been largely supposed to be positive for the CD133 antigen, even though no clear correlation has been established between its expression and function in ECFCs. We postulated that CD133 in ECFCs might be expressed intracellularly, and could participate to vasculogenic properties. ECFCs extracted from cord blood were used either fresh (n = 4) or frozen (n = 4), at culture days <30, to investigate the intracellular presence of CD133 by flow cytometry and confocal analysis. Comparison with HUVEC and HAEC mature endothelial cells was carried out. Then, CD133 was silenced in ECFCs using specific siRNA (siCD133-ECFCs) or scramble siRNA (siCtrl-ECFCs). siCD133-ECFCs (n = 12), siCtrl-ECFCs (n = 12) or PBS (n = 12) were injected in a hind-limb ischemia nude mouse model and vascularization was quantified at day 14 with H&E staining and immunohistochemistry for CD31. Results of flow cytometry and confocal microscopy evidenced the positivity of CD133 in ECFCs after permeabilization compared with not permeabilized ECFCs (p < 0.001) and mature endothelial cells (p < 0.03). In the model of mouse hind-limb ischemia, silencing of CD133 in ECFCs significantly abolished post-ischemic revascularization induced by siCtrl-ECFCs; indeed, a significant reduction in cutaneous blood flows (p = 0.03), capillary density (CD31) (p = 0.01) and myofiber regeneration (p = 0.04) was observed. Also, a significant necrosis (p = 0.02) was observed in mice receiving siCD133-ECFCs compared to those treated with siCtrl-ECFCs. In conclusion, our work describes for the first time the intracellular expression of the stemness marker CD133 in ECFCs. This feature could resume the discrepancies found in the literature concerning CD133 positivity and ontogeny in endothelial progenitors.

Indexed as

Gene Expression RegulationNeovascularization, PhysiologicAC133 AntigenAnimalsAntigens, DifferentiationEndothelial Progenitor CellsHeterograftsHindlimbHumansHuman Umbilical Vein Endothelial CellsIschemiaMaleMiceMice, NudeStem Cell TransplantationAC133 AntigenAntigens, DifferentiationPROM1 protein, humanAngiogenesisCD133ECFCEndothelial colony forming cellsEndothelial progenitorProminin-1Stem cellsStemness

Identifiers

PMID30879244
OpenAlexW2921377925

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.