Evidence map›Paper›PMID 28211362›Full record

ArticleBiomedical materials (Bristol, England)2017

Marrow-isolated adult multilineage inducible cells embedded within a biologically-inspired construct promote recovery in a mouse model of peripheral vascular disease.

Cristina Grau-Monge, Gaëtan J-R Delcroix, Andrea Bonnin-Marquez, Mike Valdes, Ead Lewis Mazen Awadallah, Daniel F Quevedo, Maxime R Armour, Ramon B Montero, Paul C Schiller, Fotios M Andreopoulos and 1 more

Abstract read
In one paragraph

Article in Biomedical materials (Bristol, England), 2017. 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
0.6field-weighted citation impact, top 31% 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, 13 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

11 authors at 2 institutions in 1 country.

Cristina Grau-MongeDepartment of Orthopaedics, University of Miami Miller School of Medicine, FL, United States of America.
Gaëtan J-R DelcroixDepartment of Orthopaedics, University of Miami Miller School of Medicine, FL, United States of America.
Andrea Bonnin-MarquezGeriatric Research, Education, and Clinical Center and Research Service, Bruce W. Carter VAMC, Miami, FL, United States of America.
Mike ValdesDepartment of Biomedical Engineering, University of Miami College of Engineering, FL, United States of America.
Ead Lewis Mazen AwadallahDepartment of Biomedical Engineering, University of Miami College of Engineering, FL, United States of America.
Daniel F QuevedoDepartment of Biomedical Engineering, University of Miami College of Engineering, FL, United States of America.
Maxime R ArmourDepartment of Biomedical Engineering, University of Miami College of Engineering, FL, United States of America.
Ramon B MonteroDepartment of Biomedical Engineering, University of Miami College of Engineering, FL, United States of America.
Paul C SchillerDepartment of Orthopaedics, University of Miami Miller School of Medicine, FL, United States of America.
Fotios M AndreopoulosDepartment of Biomedical Engineering, University of Miami College of Engineering, FL, United States of America.
Gianluca D'IppolitoDepartment of Orthopaedics, University of Miami Miller School of Medicine, FL, United States of America.
University of Miami · USBruce W. Carter VA Medical Center · US

Funding

MIAMI cellular-based constructs for vessel regeneration in an aged mouse model ofR21AG044624 · NIA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI D'IPPOLITO, GIANLUCA · 2014 to 2015
$407k
Mechanisms of Stem Cell Self-Renewal and AgingI01BX000952 · VA · MIAMI VA HEALTH CARE SYSTEM · PI SCHILLER, PAUL CHRISTIAN · 2012 to 2015
–
BLRD VA I01 BX000952NIA NIH HHS R21 AG044624
6 · The paper itself

Abstract

Peripheral vascular disease is one of the major vascular complications in individuals suffering from diabetes and in the elderly that is associated with significant burden in terms of morbidity and mortality. Stem cell therapy is being tested as an attractive alternative to traditional surgery to prevent and treat this disorder. The goal of this study was to enhance the protective and reparative potential of marrow-isolated adult multilineage inducible (MIAMI) cells by incorporating them within a bio-inspired construct (BIC) made of two layers of gelatin B electrospun nanofibers. We hypothesized that the BIC would enhance MIAMI cell survival and engraftment, ultimately leading to a better functional recovery of the injured limb in our mouse model of critical limb ischemia compared to MIAMI cells used alone. Our study demonstrated that MIAMI cell-seeded BIC resulted in a wide range of positive outcomes with an almost full recovery of blood flow in the injured limb, thereby limiting the extent of ischemia and necrosis. Functional recovery was also the greatest when MIAMI cells were combined with BICs, compared to MIAMI cells alone or BICs in the absence of cells. Histology was performed 28 days after grafting the animals to explore the mechanisms at the source of these positive outcomes. We observed that our critical limb ischemia model induces an extensive loss of muscular fibers that are replaced by intermuscular adipose tissue (IMAT), together with a highly disorganized vascular structure. The use of MIAMI cells-seeded BIC prevented IMAT infiltration with some clear evidence of muscular fibers regeneration.

Indexed as

Adipose TissueAnimalsBiocompatible MaterialsCells, CulturedDisease Models, AnimalExtremitiesGelatinHumansInduced Pluripotent Stem CellsIschemiaMaleMaterials TestingMiceMice, Inbred BALB CMuscle, Smooth, VascularNanofibersBiocompatible MaterialsGelatin

Identifiers

PMID28211362
PMCPMC5373662
OpenAlexW2589002624

What OpenQuestion holds

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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.