Evidence map›Paper›PMID 33664277›Full record

ArticleScientific reports2021

Intra-vital imaging of mesenchymal stromal cell kinetics in the pulmonary vasculature during infection.

Claire H Masterson, Arata Tabuchi, Grace Hogan, Glenn Fitzpatrick, Steven W Kerrigan, Mirjana Jerkic, Wolfgang M Kuebler, John G Laffey, Gerard F Curley

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. 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
5.0field-weighted citation impact, top 4% 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, 47 citations in OpenAlex.

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  5. Integrative Approaches to Treating Cellular Senescence in Kidney Disease.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  9. From development to regeneration: the endothelial interface in lung injury and repair.American journal of physiology. Lung cellular and molecular physiology · 2025
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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

9 authors at 5 institutions in 3 countries.

Claire H MastersonDepartment of Anesthesia, Keenan Research Centre for Biomedical Science of St Michael's Hospital, St. Michael'sHospital, 30 Bond Street, Toronto, Canada.
Arata TabuchiDepartment of Surgery, Keenan Research Centre for Biomedical Science of St Michael's Hospital, St. Michael'sHospital, 30 Bond Street, Toronto, Canada.
Grace HoganDepartment of Anesthesia, Keenan Research Centre for Biomedical Science of St Michael's Hospital, St. Michael'sHospital, 30 Bond Street, Toronto, Canada.
Glenn FitzpatrickDepartment of Anaesthesia and Critical Care, Royal College of Surgeons in Ireland, Dublin, Ireland.
Steven W KerriganDepartment of Anaesthesia and Critical Care, Royal College of Surgeons in Ireland, Dublin, Ireland.
Mirjana JerkicDepartment of Anesthesia, Keenan Research Centre for Biomedical Science of St Michael's Hospital, St. Michael'sHospital, 30 Bond Street, Toronto, Canada.
Wolfgang M KueblerDepartment of Surgery, Keenan Research Centre for Biomedical Science of St Michael's Hospital, St. Michael'sHospital, 30 Bond Street, Toronto, Canada.
John G LaffeyDepartment of Anesthesia, Keenan Research Centre for Biomedical Science of St Michael's Hospital, St. Michael'sHospital, 30 Bond Street, Toronto, Canada.
Gerard F CurleyDepartment of Anesthesia, Keenan Research Centre for Biomedical Science of St Michael's Hospital, St. Michael'sHospital, 30 Bond Street, Toronto, Canada. gercurley@rcsi.ie.
Royal College of Surgeons in Ireland · IESt. Michael's Hospital · CAUniversity of Toronto · CACharité - Universitätsmedizin Berlin · DEOllscoil na Gaillimhe – University of Galway · IE

Funding

CIHR CIHR-312714
6 · The paper itself

Abstract

Mesenchymal stem/stromal cells (MSCs) have demonstrated efficacy in pre-clinical models of inflammation and tissue injury, including in models of lung injury and infection. Rolling, adhesion and transmigration of MSCs appears to play a role during MSC kinetics in the systemic vasculature. However, a large proportion of MSCs become entrapped within the lungs after intravenous administration, while the initial kinetics and the site of arrest of MSCs in the pulmonary vasculature are unknown. We examined the kinetics of intravascularly administered MSCs in the pulmonary vasculature using a microfluidic system in vitro and intra-vital microscopy of intact mouse lung. In vitro, MSCs bound to endothelium under static conditions but not under laminar flow. VCAM-1 antibodies did not affect MSC binding. Intravital microscopy demonstrated MSC arrest at pulmonary micro-vessel bifurcations due to size obstruction. Retention of MSCs in the pulmonary microvasculature was increased in Escherichia coli-infected animals. Trapped MSCs deformed over time and appeared to release microvesicles. Labelled MSCs retained therapeutic efficacy against pneumonia. Our results suggest that MSCs are physically obstructed in pulmonary vasculature and do not display properties of rolling/adhesion, while retention of MSCs in the infected lung may require receptor interaction.

Indexed as

Mesenchymal Stem Cell TransplantationAdministration, IntravenousAnimalsBlood VesselsCardiovascular SystemDisease Models, AnimalHumansKineticsLungMesenchymal Stem CellsMicePneumonia

Identifiers

PMID33664277
PMCPMC7933415
OpenAlexW3134956792

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.