Evidence map›Paper›PMID 28962669›Full record

ArticleStem cell research & therapy2017

Sonic hedgehog (SHH) signaling improves the angiogenic potential of Wharton's jelly-derived mesenchymal stem cells (WJ-MSC).

Gabriela Zavala, Catalina P Prieto, Andrea A Villanueva, Verónica Palma

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

12 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  3. Review
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  8. Dental Pulp Stem Cell-Derived Secretome and Its Regenerative Potential.International journal of molecular sciences · 2021
    Review
  9. Stem Cell Therapy for Burns: Story so Far.Biologics : targets & therapy · 2021
    Review
  10. Article
  11. Review
  12. Article
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

4 authors at 1 institution in 1 country.

Gabriela ZavalaLaboratory of Stem Cells and Development, Faculty of Sciences, Universidad de Chile, Las Palmeras 3425, Ñuñoa, 7800003, Santiago, Chile.
Catalina P PrietoLaboratory of Stem Cells and Development, Faculty of Sciences, Universidad de Chile, Las Palmeras 3425, Ñuñoa, 7800003, Santiago, Chile.
Andrea A VillanuevaLaboratory of Stem Cells and Development, Faculty of Sciences, Universidad de Chile, Las Palmeras 3425, Ñuñoa, 7800003, Santiago, Chile.
Verónica PalmaLaboratory of Stem Cells and Development, Faculty of Sciences, Universidad de Chile, Las Palmeras 3425, Ñuñoa, 7800003, Santiago, Chile. vpalma@uchile.cl.ORCID 0000-0002-4320-7525
University of Chile · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWharton's jelly-derived mesenchymal stem cells (WJ-MSC) show remarkable therapeutic potential to repair tissue upon injury via paracrine signaling by secreting diverse trophic factors that promote angiogenesis. However, the mechanisms and signaling pathways that regulate the induction of these specific factors are still mostly unknown. Emerging evidence suggests that Sonic hedgehog (SHH) plays a central role in angiogenesis and tissue maintenance. However, its contribution to the angiogenic potential of MSC has not been fully addressed. The aim of this work was to characterize the expression of the SHH pathway components in WJ-MSC primary cultures and to evaluate their angiogenic responsiveness to SHH signaling.

methodsPrimary cell cultures obtained from human umbilical cords were treated with pharmacological modulators of the SHH pathway. We evaluated the modulation of diverse trophic factors in cell lysates, conditioned medium, and functional in vitro assays. In addition, we determined the angiogenic potential of the SHH pathway in the chicken chorioallantoic membrane, an in vivo model.

resultsOur results show that WJ-MSC express components of the canonical SHH pathway and are activated by its signaling. In fact, we provide evidence of basal autocrine/paracrine SHH signaling in WJ-MSC. SHH pathway stimulation promotes the secretion of angiogenic factors such as activin A, angiogenin, angiopoietin 1, granulocyte-macrophage colony-stimulating factor, matrix metallometallopeptidase -9, and urokinase-type plasminogen activator, enhancing the pro-angiogenic capabilities of WJ-MSC both in vitro and in vivo.

conclusionWJ-MSC are a cell population responsive to SHH pathway stimulation. Basal SHH signaling is in part responsible for the angiogenic inductive properties of WJ-MSC. Overall, exogenous activation of the SHH pathway enhances the angiogenic properties of WJ-MSC, making this cell population an ideal target for treating tissue injury.

Indexed as

Neovascularization, PhysiologicActivinsAngiopoietin-1AnimalsCell DifferentiationCell LineCells, CulturedChickensFemaleGranulocyte-Macrophage Colony-Stimulating FactorHedgehog ProteinsHumansMatrix Metalloproteinase 9Mesenchymal Stem CellsMicePlasminogen Activatorsactivin AActivinsAngiopoietin-1Granulocyte-Macrophage Colony-Stimulating FactorHedgehog ProteinsMatrix Metalloproteinase 9Plasminogen ActivatorsAngiogenesisCAM assayNiche factorSonic hedgehogUmbilical cordVEGFWJ-MSC

Identifiers

PMID28962669
PMCPMC5622478
OpenAlexW2760053683

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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.