Evidence map›Paper›PMID 34149687›Full record

ReviewFrontiers in immunology2021

The Macrophage Response Is Driven by Mesenchymal Stem Cell-Mediated Metabolic Reprogramming.

Noymar Luque-Campos, Felipe A Bustamante-Barrientos, Carolina Pradenas, Cynthia García, María Jesús Araya, Candice Bohaud, Rafael Contreras-López, Roberto Elizondo-Vega, Farida Djouad, Patricia Luz-Crawford and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 6% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

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  3. TPx Protein ofPathogens (Basel, Switzerland) · 2026
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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

11 authors at 6 institutions in 2 countries.

Noymar Luque-CamposLaboratorio de Inmunología Celular y Molecular, Facultad de Medicina, Universidad de los Andes, Santiago, Chile.
Felipe A Bustamante-BarrientosLaboratorio de Inmunología Celular y Molecular, Facultad de Medicina, Universidad de los Andes, Santiago, Chile.
Carolina PradenasLaboratorio de Inmunología Celular y Molecular, Facultad de Medicina, Universidad de los Andes, Santiago, Chile.
Cynthia GarcíaLaboratorio de Inmunología Celular y Molecular, Facultad de Medicina, Universidad de los Andes, Santiago, Chile.
María Jesús ArayaLaboratorio de Inmunología Celular y Molecular, Facultad de Medicina, Universidad de los Andes, Santiago, Chile.
Candice BohaudIRMB, Univ Montpellier, INSERM, Montpellier, France.
Rafael Contreras-LópezIRMB, Univ Montpellier, INSERM, Montpellier, France.
Roberto Elizondo-VegaLaboratorio de Biología Celular, Departamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile.
Farida DjouadIRMB, Univ Montpellier, INSERM, Montpellier, France.
Patricia Luz-CrawfordLaboratorio de Inmunología Celular y Molecular, Facultad de Medicina, Universidad de los Andes, Santiago, Chile.
Ana María Vega-LetterCentro de Investigación e Innovación Biomédica, Universidad de los Andes, Santiago, Chile.
Universidad de Los Andes, Chile · CLInserm · FRClínica Las Condes · CLUniversité de Montpellier · FRUniversity of Chile · CLUniversity of Concepción · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) are multipotent adult stromal cells widely studied for their regenerative and immunomodulatory properties. They are capable of modulating macrophage plasticity depending on various microenvironmental signals. Current studies have shown that metabolic changes can also affect macrophage fate and function. Indeed, changes in the environment prompt phenotype change. Therefore, in this review, we will discuss how MSCs orchestrate macrophage's metabolic plasticity and the impact on their function. An improved understanding of the crosstalk between macrophages and MSCs will improve our knowledge of MSC's therapeutic potential in the context of inflammatory diseases, cancer, and tissue repair processes in which macrophages are pivotal.

Indexed as

Cell CommunicationCell PlasticityCellular ReprogrammingEnergy MetabolismAnimalsCellular MicroenvironmentHumansInflammation MediatorsMacrophagesMesenchymal Stem CellsPhenotypeSignal TransductionInflammation Mediatorsautoimmunitycancermacrophagesmesenchymal stem cellsmetabolismtissue repair and regeneration

Identifiers

PMID34149687
PMCPMC8213396
OpenAlexW3166294177

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.