Evidence map›Paper›PMID 35563809›Full record

ArticleCells2022

The Autophagy Protein Pacer Positively Regulates the Therapeutic Potential of Mesenchymal Stem Cells in a Mouse Model of DSS-Induced Colitis.

Cristian A Bergmann, Sebastian Beltran, Ana Maria Vega-Letter, Paola Murgas, Maria Fernanda Hernandez, Laura Gomez, Luis Labrador, Bastián I Cortés, Cristian Poblete, Cristobal Quijada and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-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

11 citing papers in PubMed, 14 citations in OpenAlex.

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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

13 authors at 4 institutions in 1 country.

Cristian A BergmannCenter for Integrative Biology (CIB), Faculty of Science, Universidad Mayor, Santiago 7500000, Chile.ORCID 0000-0001-7564-9742
Sebastian BeltranCenter for Integrative Biology (CIB), Faculty of Science, Universidad Mayor, Santiago 7500000, Chile.
Ana Maria Vega-LetterLaboratorio de Inmunología Celular y Molecular, Centro de Investigación Biomédica, Facultad de Medicina, Universidad de Los Andes, Santiago 7620001, Chile.
Paola MurgasCenter for Integrative Biology (CIB), Faculty of Science, Universidad Mayor, Santiago 7500000, Chile.ORCID 0000-0001-9601-9096
Maria Fernanda HernandezCenter for Integrative Biology (CIB), Faculty of Science, Universidad Mayor, Santiago 7500000, Chile.
Laura GomezCenter for Integrative Biology (CIB), Faculty of Science, Universidad Mayor, Santiago 7500000, Chile.
Luis LabradorCenter for Integrative Biology (CIB), Faculty of Science, Universidad Mayor, Santiago 7500000, Chile.ORCID 0000-0002-0511-2015
Bastián I CortésCenter for Integrative Biology (CIB), Faculty of Science, Universidad Mayor, Santiago 7500000, Chile.
Cristian PobleteLaboratorio de Morfofisiopatología y Citodiagnóstico, Escuela de Tecnología Médica, Facultad de Ciencias, Universidad Mayor, Santiago 7500000, Chile.ORCID 0000-0003-0903-7400
Cristobal QuijadaServicio de Anatomía Patológica, Hospital Clínico de la Universidad de Chile, Santiago 8380456, Chile.
Flavio CarrionPrograma de Inmunología Translacional, Facultad de Medicina, Universidad del Desarrollo Clínica Alemana, Santiago 7590943, Chile.ORCID 0000-0002-4086-6867
Ute WoehlbierCenter for Integrative Biology (CIB), Faculty of Science, Universidad Mayor, Santiago 7500000, Chile.ORCID 0000-0003-3114-9708
Patricio A ManqueCenter for Integrative Biology (CIB), Faculty of Science, Universidad Mayor, Santiago 7500000, Chile.
Universidad Mayor · CLHospital Clínico de la Universidad de Chile · CLUniversidad de Los Andes, Chile · CLUniversidad de Santiago de Chile · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSC) have emerged as a promising tool to treat inflammatory diseases, such as inflammatory bowel disease (IBD), due to their immunoregulatory properties. Frequently, IBD is modeled in mice by using dextran sulfate sodium (DSS)-induced colitis. Recently, the modulation of autophagy in MSC has been suggested as a novel strategy to improve MSC-based immunotherapy. Hence, we investigated a possible role of Pacer, a novel autophagy enhancer, in regulating the immunosuppressive function of MSC in the context of DSS-induced colitis. We found that Pacer is upregulated upon stimulation with the pro-inflammatory cytokine TNFα, the main cytokine released in the inflammatory environment of IBD. By modulating Pacer expression in MSC, we found that Pacer plays an important role in regulating the autophagy pathway in this cell type in response to TNFα stimulation, as well as in regulating the immunosuppressive ability of MSC toward T-cell proliferation. Furthermore, increased expression of Pacer in MSC enhanced their ability to ameliorate the symptoms of DSS-induced colitis in mice. Our results support previous findings that autophagy regulates the therapeutic potential of MSC and suggest that the augmentation of autophagic capacity in MSC by increasing Pacer levels may have therapeutic implications for IBD.

Indexed as

ColitisInflammatory Bowel DiseasesMesenchymal Stem CellsMesenchymal Stem Cell TransplantationAnimalsAutophagyCytokinesDextran SulfateDisease Models, AnimalMiceTumor Necrosis Factor-alphaCytokinesDextran SulfateTumor Necrosis Factor-alphaautophagycolitisinflammatory bowel diseaseKIAA0226Lmesenchymal stem cellsPACERRUBCNLtherapy

Identifiers

PMID35563809
PMCPMC9101276
OpenAlexW4225132460

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.