Evidence map›Paper›PMID 29352000›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2018

Mesenchymal Stem Cells Recruit CCR2

Katsuyuki Takeda, Tracy L Webb, Fangkun Ning, Yoshiki Shiraishi, Daniel P Regan, Lyndah Chow, Mia J Smith, Shigeru Ashino, Amanda M Guth, Sophie Hopkins and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.7field-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

33 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
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  5. Article
  6. CD317Stem cell research & therapy · 2024
    Article
  7. Apoptotic MSCs, COX2/PGE2 and clinical efficacy in Crohn fistula.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
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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

12 authors at 2 institutions in 1 country.

Katsuyuki TakedaDepartment of Pediatrics, Division of Cell Biology, National Jewish Health, Denver, CO 80206; and takedak@njhealth.org.ORCID 0000-0003-1623-3573
Tracy L WebbCenter for Immune and Regenerative Medicine, Department of Clinical Sciences, Colorado State University, Fort Collins, CO 80523.
Fangkun NingDepartment of Pediatrics, Division of Cell Biology, National Jewish Health, Denver, CO 80206; and.
Yoshiki ShiraishiDepartment of Pediatrics, Division of Cell Biology, National Jewish Health, Denver, CO 80206; and.ORCID 0000-0001-5275-6318
Daniel P ReganCenter for Immune and Regenerative Medicine, Department of Clinical Sciences, Colorado State University, Fort Collins, CO 80523.
Lyndah ChowCenter for Immune and Regenerative Medicine, Department of Clinical Sciences, Colorado State University, Fort Collins, CO 80523.ORCID 0000-0002-6413-9517
Mia J SmithCenter for Immune and Regenerative Medicine, Department of Clinical Sciences, Colorado State University, Fort Collins, CO 80523.ORCID 0000-0003-3042-5061
Shigeru AshinoDepartment of Pediatrics, Division of Cell Biology, National Jewish Health, Denver, CO 80206; and.
Amanda M GuthCenter for Immune and Regenerative Medicine, Department of Clinical Sciences, Colorado State University, Fort Collins, CO 80523.
Sophie HopkinsCenter for Immune and Regenerative Medicine, Department of Clinical Sciences, Colorado State University, Fort Collins, CO 80523.
Erwin W GelfandDepartment of Pediatrics, Division of Cell Biology, National Jewish Health, Denver, CO 80206; and.
Steven DowCenter for Immune and Regenerative Medicine, Department of Clinical Sciences, Colorado State University, Fort Collins, CO 80523.ORCID 0000-0001-5488-9464
Colorado State University · USNational Jewish Health · US

Funding

Signaling Memory in Chronic AsthmaP01HL036577 · NHLBI · NATIONAL JEWISH HEALTH · PI ALAM, RAFEUL · 1986 to 2011
$18.7M
Biomedical Research Training for VeterinariansT32OD010437 · OD · COLORADO STATE UNIVERSITY · PI Gregg A Dean, KELLY S SANTANGELO · 2012 to 2026
$6.2M
Naturally Occurring T Regulatory Cells Control Airway HyperresponsivenessR01AI077609 · NIAID · NATIONAL JEWISH HEALTH · PI GELFAND, ERWIN WILLIAM · 2009 to 2013
$2.3M
Veterinary Pre-Doctoral Research Scholars ProgramT32OD012201 · OD · COLORADO STATE UNIVERSITY · PI VANDEWOUDE, SUE · 2013 to 2019
$795k
Elucidating the role and regulation of periostin in therapy-induced chemoresistance in metastatic breast cancerK01OD022982 · OD · COLORADO STATE UNIVERSITY · PI REGAN, DANIEL PATRICK · 2016 to 2021
$720k
Evolution of Dendritic Cell Dysfunction in FIV InfectionK08AI071724 · NIAID · COLORADO STATE UNIVERSITY · PI WEBB, TRACY L · 2008 to 2012
$529k
NHLBI NIH HHS P01 HL036577NIAID NIH HHS K08 AI071724NIAID NIH HHS R01 AI077609NIH HHS K01 OD022982NIH HHS T32 OD010437NIH HHS T32 OD012201
6 · The paper itself

Abstract

Mesenchymal stem cells (MSC) exert immune modulatory properties and previous studies demonstrated suppressive effects of MSC treatment in animal models of allergic airway inflammation. However, the underlying mechanisms have not been fully elucidated. We studied the role of MSC in immune activation and subsequent recruitment of monocytes in suppressing airway hyperresponsiveness and airway inflammation using a mouse model of allergic airway inflammation. MSC administration prior to or after allergen challenge inhibited the development of airway inflammation in allergen-sensitized mice. This was accompanied by an influx of CCR2-positive monocytes, which were localized around injected MSC in the lungs. Notably, IL-10-producing monocytes and/or macrophages were also increased in the lungs. Systemic administration of liposomal clodronate or a CCR2 antagonist significantly prevented the suppressive effects of MSC. Activation of MSC by IFN-γ leading to the upregulation of CCL2 expression was essential for the suppressive effects, as administration of wild-type MSC into IFN-γ-deficient recipients, or IFN-γ receptor-deficient or CCL2-deficient MSC into wild-type mice failed to suppress airway inflammation. These results suggest that MSC activation by IFN-γ, followed by increased expression of CCL2 and recruitment of monocytes to the lungs, is essential for suppression by MSC in allergen-induced airway hyperresponsiveness and airway inflammation.

Indexed as

AnimalsCell MovementFemaleInflammationMesenchymal Stem CellsMiceMice, Inbred C57BLMonocytesReceptors, CCR2Respiratory HypersensitivityCcr2 protein, mouseReceptors, CCR2

Identifiers

PMID29352000
PMCPMC5809262
OpenAlexW2783676704

What OpenQuestion holds

Textmetadata
LicenceTDM
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.