Evidence map›Paper›PMID 23553740›Full record

ArticleJournal of orthopaedic research : official publication of the Orthopaedic Research Society2013

Human myogenic endothelial cells exhibit chondrogenic and osteogenic potentials at the clonal level.

Bo Zheng, Guangheng Li, William C W Chen, Bridget M Deasy, Jonathan B Pollett, Bin Sun, Lauren Drowley, Burhan Gharaibeh, Arvydas Usas, Bruno Péault and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2013. 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
1.7field-weighted citation impact, top 17% 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, 20 citations in OpenAlex.

  1. Stem Cells and Bone Tissue Engineering.Life (Basel, Switzerland) · 2024
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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 5 institutions in 2 countries.

Bo ZhengStem Cell Research Center, Department of Orthopaedic Surgery, University of Pittsburgh School of Medicine, Bridgeside Point II, Suite 206, 450 Technology Drive, Pittsburgh, Pennsylvania 15219, USA.
Guangheng Li
William C W Chen
Bridget M Deasy
Jonathan B Pollett
Bin Sun
Lauren Drowley
Burhan Gharaibeh
Arvydas Usas
Bruno Péault
Johnny Huard
Point Park University · USUniversity of Pittsburgh · USChildren's Hospital of Pittsburgh · USMcGowan Institute for Regenerative Medicine · USUniversity of Edinburgh · GB

Funding

Preclinical Gene Therapy in a Large Animal Model of DMDU54AR050733 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HUARD, JOHNNY · 2003 to 2008
$7.7M
Muscle Based Tissue Engineering to Improve Bone HealingR01DE013420 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HUARD, JOHNNY · 2001 to 2010
$3.6M
Muscle regeneration through stem cell transplantationR01AR049684 · NIAMS · CHILDREN'S HOSP PITTSBURGH/UPMC HLTH SYS · PI HUARD, JOHNNY · 2002 to 2006
$1.4M
Medical Research Council G1000816NIAMS NIH HHS IU54AR050733-01NIAMS NIH HHS R01 AR049684NIAMS NIH HHS R01-AR049684NIAMS NIH HHS U54 AR050733NIDCR NIH HHS R01 DE013420NIDCR NIH HHS R01-DE13420-06
6 · The paper itself

Abstract

We have previously reported the high regenerative potential of murine muscle-derived stem cells (mMDSCs) that are capable of differentiating into multiple mesodermal cell lineages, including myogenic, endothelial, chondrocytic, and osteoblastic cells. Recently, we described a putative human counterpart of mMDSCs, the myogenic endothelial cells (MECs), in adult human skeletal muscle, which efficiently repair/regenerate the injured and dystrophic skeletal muscle as well as the ischemic heart in animal disease models. Nevertheless it remained unclear whether human MECs, at the clonal level, preserve mMDSC-like chondrogenic and osteogenic potentials and classic stem cell characteristics including high proliferation and resistance to stress. Herein, we demonstrated that MECs, sorted from fresh postnatal human skeletal muscle biopsies, can be grown clonally and exhibit robust resistance to oxidative stress with no tumorigeneity. MEC clones were capable of differentiating into chondrocytes and osteoblasts under inductive conditions in vitro and participated in cartilage and bone formation in vivo. Additionally, adipogenic and angiogenic potentials of clonal MECs (cMECs) were observed. Overall, our study showed that cMECs not only display typical properties of adult stem cells but also exhibit chondrogenic and osteogenic capacities in vitro and in vivo, suggesting their potential applications in articular cartilage and bone repair/regeneration.

Indexed as

AdipocytesAdultAnimalsBiopsyCell DifferentiationCell ProliferationCells, CulturedChondrocytesChondrogenesisEndotheliumHumansIn Vitro TechniquesMaleMiceMice, SCIDMuscle Development

Identifiers

PMID23553740
PMCPMC4360901
OpenAlexW1559432338

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.