Evidence map›Paper›PMID 23629940›Full record

ArticleJournal of biomedical materials research. Part A2013

Characterization of chondrocyte scaffold carriers for cell-based gene therapy in articular cartilage repair.

Wei Shui, Liangjun Yin, Jeffrey Luo, Ruidong Li, Wenwen Zhang, Jiye Zhang, Wei Huang, Ning Hu, Xi Liang, Zhong-Liang Deng and 6 more

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.8field-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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Review
  6. Review
  7. Article
  8. Gene therapy for chondral and osteochondral regeneration: is the future now?Cellular and molecular life sciences : CMLS · 2018
    Review
  9. Article
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  16. Destabilization of heterologous proteins mediated by the GSK3β phosphorylation domain of the β-catenin protein.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2013
    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

16 authors at 5 institutions in 2 countries.

Wei ShuiDepartment of Orthopaedic Surgery of the Affiliated Hospitals, Chongqing Medical University, Chongqing 400016, China; Molecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine, The University of Chicago Medical Center, Chicago, Illinois 60637.
Liangjun Yin
Jeffrey Luo
Ruidong Li
Wenwen Zhang
Jiye Zhang
Wei Huang
Ning Hu
Xi Liang
Zhong-Liang Deng
Zhenming Hu
Lewis L Shi
Hue H Luu
Rex C Haydon
Tong-Chuan He
Sherwin H Ho
University of Chicago · USDalian Medical University · CNSecond Affiliated Hospital of Chongqing Medical University · CNFirst Affiliated Hospital of Chongqing Medical University · CNUniversity of Chicago Medical Center · US

Funding

Regulation of beta-Catenin Signaling by Tyrosine PhosphorylationR01CA106569 · NCI · UNIVERSITY OF CHICAGO · PI HE, TONG-CHUAN · 2006 to 2010
$1.3M
NCI NIH HHS R01 CA106569
6 · The paper itself

Abstract

Articular cartilage lesions in the knee are common injuries. Chondrocyte transplant represents a promising therapeutic modality for articular cartilage injuries. Here, we characterize the viability and transgene expression of articular chondrocytes cultured in three-dimensional scaffolds provided by four types of carriers. Articular chondrocytes are isolated from rabbit knees and cultured in four types of scaffolds: type I collagen sponge, fibrin glue, hyaluronan, and open-cell polylactic acid (OPLA). The cultured cells are transduced with adenovirus expressing green fluorescence protein (AdGFP) and luciferase (AdGL3-Luc). The viability and gene expression in the chondrocytes are determined with fluorescence microscopy and luciferase assay. Cartilage matrix production is assessed by Alcian blue staining. Rabbit articular chondrocytes are effectively infected by AdGFP and exhibited sustained GFP expression. All tested scaffolds support the survival and gene expression of the infected chondrocytes. However, the highest transgene expression is observed in the OPLA carrier. At 4 weeks, Alcian blue-positive matrix materials are readily detected in OPLA cultures. Thus, our results indicate that, while all tested carriers can support the survival of chondrocytes, OPLA supports the highest transgene expression and is the most conductive scaffold for matrix production, suggesting that OPLA may be a suitable scaffold for cell-based gene therapy of articular cartilage repairs.

Indexed as

Genetic TherapyWound HealingAdenoviridaeAnimalsCartilage, ArticularCell SeparationCell SurvivalChondrocytesExtracellular MatrixGene Expression RegulationGenetic VectorsGene Transfer TechniquesHEK293 CellsHumansLactic AcidMaleLactic AcidPolyesterspoly(lactide)Polymersarticular cartilageautologous chondrocyte implantationchondrocyteex vivo gene therapyopen-cell poly lactic acid (OPLA)scaffold carrier

Identifiers

PMID23629940
PMCPMC4056444
OpenAlexW1913082307

What OpenQuestion holds

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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.