Evidence map›Paper›PMID 37981698›Full record

ArticleStem cell research & therapy2023

Lactate: an alternative pathway for the immunosuppressive properties of mesenchymal stem/stromal cells.

Carolina Pradenas, Noymar Luque-Campos, Karina Oyarce, Rafael Contreras-Lopez, Felipe A Bustamante-Barrientos, Andrés Bustos, Felipe Galvez-Jiron, María Jesús Araya, Catalina Asencio, Raúl Lagos and 12 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

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  13. IntratumoralFrontiers in cellular and infection microbiology · 2024
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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

22 authors at 7 institutions in 2 countries.

Carolina Pradenas *Laboratorio de Biología Celular, Departamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile.
Noymar Luque-Campos *Centro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile.
Karina Oyarce *Facultad de Medicina y Ciencia, Universidad San Sebastián, Concepción, Chile.
Rafael Contreras-LopezIRMB, University of Montpellier, INSERM, 34295, Montpellier, France.
Felipe A Bustamante-BarrientosCentro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile.
Andrés BustosLaboratorio de Biología Celular, Departamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile.
Felipe Galvez-JironCentro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile.
María Jesús ArayaCentro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile.
Catalina AsencioCentro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile.
Raúl LagosLaboratorio de Biología Celular, Departamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile.
Yeimi Herrera-LunaCentro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile.
Daouda Abba MoussaIRMB, University of Montpellier, INSERM, 34295, Montpellier, France.
Charlotte Nicole HillCentro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile.
Eliana Lara-BarbaCentro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile.
Claudia AltamiranoIMPACT, Center of Interventional Medicine for Precision and Advanced Cellular Therapy, Santiago, Chile.
Alexander OrtloffDepartamento de Ciencias Veterinarias y Salud Pública, Facultad de Recursos Naturales, Universidad Católica de Temuco, Temuco, Chile.
Yessia Hidalgo-FadicIMPACT, Center of Interventional Medicine for Precision and Advanced Cellular Therapy, Santiago, Chile.
Ana María Vega-LetterCentro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile.
María de Los Ángeles García-RoblesLaboratorio de Biología Celular, Departamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile.
Farida DjouadIRMB, University of Montpellier, INSERM, 34295, Montpellier, France. farida.djouad@inserm.fr.
Patricia Luz-CrawfordCentro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago, Chile. pluz@uandes.cl.
Roberto Elizondo-VegaLaboratorio de Biología Celular, Departamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile. relizondo@udec.cl.
Universidad de Los Andes, Chile · CLUniversity of Concepción · CLUniversité de Montpellier · FRMillennium Institute on Immunology and Immunotherapy · CLPontificia Universidad Católica de Valparaíso · CLSan Sebastián University · CLTemuco Catholic University · CL

Funding

Agencia Nacional de Investigación y Desarrollo #FB210024Agencia Nacional de Investigación y Desarrollo fondecyt iniciacion 11190690Agencia Nacional de Investigación y Desarrollo fondecyt regular 1211353Agencia Nacional de Investigación y Desarrollo IMPACT
6 · The paper itself

Abstract

backgroundThe metabolic reprogramming of mesenchymal stem/stromal cells (MSC) favoring glycolysis has recently emerged as a new approach to improve their immunotherapeutic abilities. This strategy is associated with greater lactate release, and interestingly, recent studies have proposed lactate as a functional suppressive molecule, changing the old paradigm of lactate as a waste product. Therefore, we evaluated the role of lactate as an alternative mediator of MSC immunosuppressive properties and its contribution to the enhanced immunoregulatory activity of glycolytic MSCs. MATERIALS AND

methodsMurine CD4

resultsOur results showed that 50 mM of exogenous L-lactate inhibited the proliferation rate and phenotype of CD4

conclusionThese findings identify a new MSC immunosuppressive pathway that is independent of the classical suppressive mechanism and demonstrated that the enhanced suppressive and therapeutic abilities of glycolytic MSCs depend at least in part on lactate production.

Indexed as

Lactic AcidMesenchymal Stem CellsAnimalsCell DifferentiationHumansImmunosuppressive AgentsMaleMiceMice, Inbred C57BLImmunosuppressive AgentsLactic AcidGlycolytic metabolismImmunosuppressionLactate dehydrogenase, lactateMesenchymal stem/stromal cellsTh1 and Th17 cells

Identifiers

PMID37981698
PMCPMC10659074
OpenAlexW4388809058

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.