Evidence map›Paper›PMID 25177794›Full record

ArticleJournal of visualized experiments : JoVE2014

Isolation of blood-vessel-derived multipotent precursors from human skeletal muscle.

William C W Chen, Arman Saparov, Mirko Corselli, Mihaela Crisan, Bo Zheng, Bruno Péault, Johnny Huard

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Pericytes as a Source of Osteogenic Cells in Bone Fracture Healing.International journal of molecular sciences · 2019
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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

7 authors at 6 institutions in 5 countries.

William C W ChenStem Cell Research Center, Department of Bioengineering and Orthopedic Surgery, University of Pittsburgh; chc88@pitt.edu.
Arman SaparovDepartment of Orthopedic Surgery, University of Pittsburgh; Nazarbayev University Research and Innovation System, Nazarbayev University.
Mirko CorselliDepartment of Orthopaedic Surgery, UCLA Orthopaedic Hospital and the Orthopaedic Hospital Research Center, University of California at Los Angeles.
Mihaela CrisanDepartment of Cell Biology, Erasmus MC Stem Cell Institute.
Bo ZhengOHSU Center for Regenerative Medicine, Oregon Health & Science University.
Bruno PéaultCentre for Cardiovascular Science and MRC Centre for Regenerative Medicine, Queen's Medical Research Institute and University of Edinburgh; David Geffen School of Medicine and the Orthopaedic Hospital Research Center, University of California at Los Angeles.
Johnny HuardStem Cell Research Center, Department of Orthopedic Surgery and McGowan Institute for Regenerative Medicine, University of Pittsburgh; jhuard@pitt.edu.
University of Pittsburgh · USMcGowan Institute for Regenerative Medicine · USMRC Centre for Regenerative Medicine · GBOregon Health & Science University · USStem Cell Institute · PAUniversity of California, Los Angeles · US

Funding

Medical Research Council G1000816
6 · The paper itself

Abstract

Since the discovery of mesenchymal stem/stromal cells (MSCs), the native identity and localization of MSCs have been obscured by their retrospective isolation in culture. Recently, using fluorescence-activated cell sorting (FACS), we and other researchers prospectively identified and purified three subpopulations of multipotent precursor cells associated with the vasculature of human skeletal muscle. These three cell populations: myogenic endothelial cells (MECs), pericytes (PCs), and adventitial cells (ACs), are localized respectively to the three structural layers of blood vessels: intima, media, and adventitia. All of these human blood-vessel-derived stem cell (hBVSC) populations not only express classic MSC markers but also possess mesodermal developmental potentials similar to typical MSCs. Previously, MECs, PCs, and ACs have been isolated through distinct protocols and subsequently characterized in separate studies. The current isolation protocol, through modifications to the isolation process and adjustments in the selective cell surface markers, allows us to simultaneously purify all three hBVSC subpopulations by FACS from a single human muscle biopsy. This new method will not only streamline the isolation of multiple BVSC subpopulations but also facilitate future clinical applications of hBVSCs for distinct therapeutic purposes.

Indexed as

AdventitiaEndothelial CellsHumansMesenchymal Stem CellsMuscle, SkeletalPericytesTunica Intima

Identifiers

PMID25177794
PMCPMC4762055
OpenAlexW2022009864

What OpenQuestion holds

Textmetadata
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.