Evidence map›Paper›PMID 32651456›Full record

ArticleScientific reports2020

PPARβ/δ-dependent MSC metabolism determines their immunoregulatory properties.

R A Contreras-Lopez, R Elizondo-Vega, M J Torres, A M Vega-Letter, N Luque-Campos, M J Paredes-Martinez, C Pradenas, G Tejedor, K Oyarce, M Salgado and 7 more

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. The PPARβ/Delta-Induced Mesenchymal Stromal Cell Secretome Has Cytoprotective Effects via ANGPTL4 in a Pre-Clinical Model of Acute Lung Inflammation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  2. Review
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  5. Article
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  7. Hematopoietic stem cell metabolism within the bone marrow niche - insights and opportunities.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  8. Article
  9. Review
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  11. Review
  12. Article
  13. Review
  14. The benefits of adipocyte metabolism in bone health and regeneration.Frontiers in cell and developmental biology · 2023
    Review
  15. Article
  16. Review
  17. PPARStem cells international · 2022
    Article
  18. Article
  19. 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

17 authors.

R A Contreras-Lopez *Centro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile.
R Elizondo-Vega *Facultad de Ciencias Biológicas, Departamento de Biología Celular, Laboratorio de Biología Celular, Universidad de Concepción, Concepción, Chile.
M J TorresEscuela de Ingeniería Bioquímica, Pontificia Universidad Católica de Valparaiso, Valparaiso, Chile.
A M Vega-LetterCells for Cells, Consorcio Regenero, Las Condes, Santiago, Chile.
N Luque-CamposCentro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile.
M J Paredes-MartinezCentro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile.
C PradenasCentro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile.
G TejedorIRMB, Univ Montpellier, INSERM, CHU Montpellier, Inserm U 1183, IRMB, Hôpital Saint-Eloi, 80 Avenue Augustin Fliche, 34295, Montpellier Cedex 5, France.
K OyarceFacultad de Ciencias de la Salud, Universidad San Sebastián, Concepción, Chile.
M SalgadoFacultad de Ciencias Biológicas, Departamento de Biología Celular, Laboratorio de Biología Celular, Universidad de Concepción, Concepción, Chile.
C JorgensenIRMB, Univ Montpellier, INSERM, CHU Montpellier, Inserm U 1183, IRMB, Hôpital Saint-Eloi, 80 Avenue Augustin Fliche, 34295, Montpellier Cedex 5, France.
M KhouryCells for Cells, Consorcio Regenero, Las Condes, Santiago, Chile.
G KronkeDepartment of Internal Medicine 3, University of Erlangen-Nuremberg, 91054, Erlangen, Germany.
M A Garcia-RoblesFacultad de Ciencias Biológicas, Departamento de Biología Celular, Laboratorio de Biología Celular, Universidad de Concepción, Concepción, Chile.
C AltamiranoEscuela de Ingeniería Bioquímica, Pontificia Universidad Católica de Valparaiso, Valparaiso, Chile.
P Luz-Crawford *Centro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile. pluz@uandes.cl.
F Djouad *IRMB, Univ Montpellier, INSERM, CHU Montpellier, Inserm U 1183, IRMB, Hôpital Saint-Eloi, 80 Avenue Augustin Fliche, 34295, Montpellier Cedex 5, France. farida.djouad@inserm.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cell (MSC)-based therapy is being increasingly considered a powerful opportunity for several disorders based on MSC immunoregulatory properties. Nonetheless, MSC are versatile and plastic cells that require an efficient control of their features and functions for their optimal use in clinic. Recently, we have shown that PPARβ/δ is pivotal for MSC immunoregulatory and therapeutic functions. However, the role of PPARβ/δ on MSC metabolic activity and the relevance of PPARβ/δ metabolic control on MSC immunosuppressive properties have never been addressed. Here, we demonstrate that PPARβ/δ deficiency forces MSC metabolic adaptation increasing their glycolytic activity required for their immunoregulatory functions on Th1 and Th17 cells. Additionally, we show that the inhibition of the mitochondrial production of ATP in MSC expressing PPARβ/δ, promotes their metabolic switch towards aerobic glycolysis to stably enhance their immunosuppressive capacities significantly. Altogether, these data demonstrate that PPARβ/δ governs the immunoregulatory potential of MSC by dictating their metabolic reprogramming and pave the way for enhancing MSC immunoregulatory properties and counteracting their versatility.

Indexed as

AnimalsBone Marrow CellsCD4-Positive T-LymphocytesCell ProliferationGene SilencingGlycolysisImmunosuppression TherapyMesenchymal Stem CellsMiceOligomycinsPPAR-betaReceptors, Cytoplasmic and NuclearTh17 CellsTh1 CellsOligomycinsPPAR-betaPpard protein, mouseReceptors, Cytoplasmic and Nuclear

Identifiers

PMID32651456
PMCPMC7351754

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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.