Evidence map›Paper›PMID 23884640›Full record

ArticleStem cells translational medicine2013

Sustained release of bone morphogenetic protein 2 via coacervate improves the osteogenic potential of muscle-derived stem cells.

Hongshuai Li, Noah Ray Johnson, Arvydas Usas, Aiping Lu, Minakshi Poddar, Yadong Wang, Johnny Huard

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Technologies to Enhance Spinal Fusion: Bench to Bedside.HSS journal : the musculoskeletal journal of Hospital for Special Surgery · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Coacervate delivery of HB-EGF accelerates healing of type 2 diabetic wounds.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
    Article
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 2 institutions in 1 country.

Hongshuai LiDepartment of Orthopaedic Surgery, University of Pittsburgh, Pittsburgh, PA, USA.
Noah Ray Johnson
Arvydas Usas
Aiping Lu
Minakshi Poddar
Yadong Wang
Johnny Huard
University of Pittsburgh · USMcGowan Institute for Regenerative Medicine · US

Funding

VARIABILITY, STABILITY & SMOOTHNESS OF WALKINGP30AG024827 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JENNIFER S BRACH · 2004 to 2026
$28.6M
Muscle Based Tissue Engineering to Improve Bone HealingR01DE013420 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HUARD, JOHNNY · 2001 to 2010
$3.6M
The Use of Coacervate Technology as a New Drug Delivery System for MusculoskeletaR21AR066206 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI HUARD, JOHNNY · 2014 to 2015
$372k
NIAMS NIH HHS R21 AR066206NIA NIH HHS P30 AG024827NIDCR NIH HHS DE013420NIDCR NIH HHS R01 DE013420
6 · The paper itself

Abstract

Muscle-derived stem cells (MDSCs) isolated from mouse skeletal muscle by a modified preplate technique exhibit long-term proliferation, high self-renewal, and multipotent differentiation capabilities in vitro. MDSCs retrovirally transduced to express bone morphogenetic proteins (BMPs) can differentiate into osteocytes and chondrocytes and enhance bone and articular cartilage repair in vivo, a feature that is not observed with nontransduced MDSCs. These results emphasize that MDSCs require prolonged exposure to BMPs to undergo osteogenic and chondrogenic differentiation. A sustained BMP protein delivery approach provides a viable and potentially more clinically translatable alternative to genetic manipulation of the cells. A unique growth factor delivery platform comprised of native heparin and a synthetic polycation, poly(ethylene argininylaspartate diglyceride) (PEAD), was used to bind, protect, and sustain the release of bone morphogenetic protein-2 (BMP2) in a temporally and spatially controlled manner. Prolonged exposure to BMP2 released by the PEAD:heparin delivery system promoted the differentiation of MDSCs to an osteogenic lineage in vitro and induced the formation of viable bone at an ectopic site in vivo. This new strategy represents an alternative approach for bone repair mediated by MDSCs while bypassing the need for gene therapy.

Indexed as

AnimalsBone Morphogenetic Protein 2Cell DifferentiationDelayed-Action PreparationsGenes, ReporterGenetic VectorsGreen Fluorescent ProteinsHeparinMiceMicellesMuscle CellsMuscle, SkeletalOsteocytesOsteogenesisPeptidesPolyestersBmp2 protein, mouseBone Morphogenetic Protein 2Delayed-Action PreparationsGreen Fluorescent ProteinsHeparinMicellesPeptidesPolyesterspoly(ethylene argininylaspartate diglyceride)Adult stem cellsBoneCellular therapyClinical translationDifferentiationHeparinMuscle stem cellsStem cell transplantation

Identifiers

PMID23884640
PMCPMC3754467
OpenAlexW2052538928

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.