Evidence map›Paper›PMID 27995034›Full record

ArticleSpringerPlus2016

Adipose-derived human stem/stromal cells: comparative organ specific mitochondrial bioenergy profiles.

Alice S Ferng, Katherine M Marsh, Jamie M Fleming, Renee F Conway, David Schipper, Naing Bajaj, Alana M Connell, Tia Pilikian, Kitsie Johnson, Ray Runyan and 3 more

Open access · diamondAbstract read
In one paragraph

Article in SpringerPlus, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 32% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
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 1 institution in 1 country.

Alice S FerngDivision of Cardiothoracic Surgery, Department of Surgery, University of Arizona College of Medicine, 1501 North Campbell Avenue, Tucson, AZ 85724 USA ; Department of Physiological Sciences, University of Arizona College of Medicine, Tucson, AZ USA ; Department of Biomedical Engineering, University of Arizona College of Medicine, Tucson, AZ USA ; University of Arizona College of Medicine, Tucson, AZ USA ; Department of Orthopaedic Surgery, University of Arizona College of Medicine, Tucson, AZ USA.
Katherine M MarshDivision of Cardiothoracic Surgery, Department of Surgery, University of Arizona College of Medicine, 1501 North Campbell Avenue, Tucson, AZ 85724 USA ; University of Arizona College of Medicine, Tucson, AZ USA.
Jamie M FlemingUniversity of Arizona College of Medicine, Tucson, AZ USA ; Department of Orthopaedic Surgery, University of Arizona College of Medicine, Tucson, AZ USA ; University of Massachusetts Medical School, UMass Memorial Health Care, Worcester, MA USA.
Renee F ConwayDepartment of Orthopaedic Surgery, University of Arizona College of Medicine, Tucson, AZ USA.
David SchipperDivision of Cardiothoracic Surgery, Department of Surgery, University of Arizona College of Medicine, 1501 North Campbell Avenue, Tucson, AZ 85724 USA.
Naing BajajDivision of Cardiothoracic Surgery, Department of Surgery, University of Arizona College of Medicine, 1501 North Campbell Avenue, Tucson, AZ 85724 USA.
Alana M ConnellDivision of Cardiothoracic Surgery, Department of Surgery, University of Arizona College of Medicine, 1501 North Campbell Avenue, Tucson, AZ 85724 USA.
Tia PilikianDivision of Cardiothoracic Surgery, Department of Surgery, University of Arizona College of Medicine, 1501 North Campbell Avenue, Tucson, AZ 85724 USA.
Kitsie JohnsonDivision of Cardiothoracic Surgery, Department of Surgery, University of Arizona College of Medicine, 1501 North Campbell Avenue, Tucson, AZ 85724 USA.
Ray RunyanDepartment of Cellular and Molecular Medicine, University of Arizona College of Medicine, Tucson, AZ USA.
Stephen M BlackUniversity of Arizona College of Medicine, Tucson, AZ USA.
John A SzivekDepartment of Orthopaedic Surgery, University of Arizona College of Medicine, Tucson, AZ USA.
Zain KhalpeyDivision of Cardiothoracic Surgery, Department of Surgery, University of Arizona College of Medicine, 1501 North Campbell Avenue, Tucson, AZ 85724 USA ; Department of Physiological Sciences, University of Arizona College of Medicine, Tucson, AZ USA ; Department of Biomedical Engineering, University of Arizona College of Medicine, Tucson, AZ USA ; University of Arizona College of Medicine, Tucson, AZ USA ; Department of Cellular and Molecular Medicine, University of Arizona College of Medicine, Tucson, AZ USA ; Banner-University Medical Center, Tucson, AZ USA.
University of Arizona · US

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Dan Theodorescu · 1985 to 2026
$110.2M
Therapeutic Mechanisms of RhoA Inhibition In Acute Lung InjuryP01HL101902 · NHLBI · AUGUSTA UNIVERSITY · PI BLACK, STEPHEN M · 2011 to 2016
$11.2M
PERINATAL REGULATION OF THE ENDOTHELIAL NOS GENER01HL060190 · NHLBI · UNIVERSITY OF MONTANA · PI Stephen M Black · 1998 to 2026
$7.1M
ROS in Pulmonary Hypertension: Role of ADMAR01HL067841 · NHLBI · UNIVERSITY OF MONTANA · PI BLACK, STEPHEN M · 2002 to 2011
$2.6M
NCI NIH HHS P30 CA023074NHLBI NIH HHS P01 HL101902NHLBI NIH HHS R01 HL060190NHLBI NIH HHS R01 HL067841
6 · The paper itself

Abstract

backgroundAdipose-derived stem/stromal cells (ASCs) isolated from the stromal vascular fraction are a source of mesenchymal stem cells that have been shown to be beneficial in many regenerative medicine applications. ASCs are an attractive source of stem cells in particular, due to their lack of immunogenicity. This study examines differences between mitochondrial bioenergetic profiles of ASCs isolated from adipose tissue of five peri-organ regions: pericardial, thymic, knee, shoulder, and abdomen.

resultsFlow cytometry showed that the majority of each ASC population isolated from the adipose tissue of 12 donors, with an n = 3 for each tissue type, were positive for MSC markers CD90, CD73, and CD105, and negative for hematopoietic markers CD34, CD11B, CD19, and CD45. Bioenergetic profiles were obtained for ASCs with an n = 4 for each tissue type and graphed together for comparison. Mitochondrial stress tests provided the following measurements: basal respiration rate (measured as oxygen consumption rate [pmol O

conclusionsThe main goal of this manuscript was to provide baseline reference values for future experiments and to compare bioenergetic potentials of ASCs isolated from adipose tissue harvested from different anatomical locations. Through an investigation of mitochondrial respiration and glycolysis, it was demonstrated that bioenergetic profiles do not significantly differ by region due to depot-dependent and donor-dependent variability. Thus, although the physiological function, microenvironment and anatomical harvest site may directly affect the characteristics of ASCs isolated from different organ regions, the ultimate utility of ASCs remains independent of the anatomical harvest site.

Indexed as

Adipose-derived stem/stromal cellsBioenergetic profilingExtracellular fluxHuman adipose tissueMesenchymal stem cellsMitochondrial bioenergeticsStromal vascular fractionTissue engineering

Identifiers

PMID27995034
PMCPMC5133220
OpenAlexW2559190554

What OpenQuestion holds

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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.