Evidence map›Paper›PMID 24133046›Full record

ArticleJournal of biomedical materials research. Part A2014

Characterization of scaffold carriers for BMP9-transduced osteoblastic progenitor cells in bone regeneration.

Wei Shui, Wenwen Zhang, Liangjun Yin, Guoxin Nan, Zhan Liao, Hongmei Zhang, Ning Wang, Ningning Wu, Xian Chen, Sheng Wen and 9 more

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 27 citations in OpenAlex.

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  20. Chitosan-based scaffolds for bone tissue engineering.Journal of materials chemistry. B · 2014
    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

19 authors at 5 institutions in 2 countries.

Wei Shui
Wenwen Zhang
Liangjun Yin
Guoxin Nan
Zhan Liao
Hongmei Zhang
Ning Wang
Ningning Wu
Xian Chen
Sheng Wen
Yunfeng He
Fang Deng
Junhui Zhang
Hue H Luu
Lewis L Shi
Zhenming Hu
Rex C Haydon
James M Mok
Tong-Chuan He
University of Chicago Medical Center · USMolecular Oncology (United States) · USChongqing Medical University · CNCentral South University · CNFirst Affiliated Hospital of Chongqing Medical University · CN

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

Successful bone tissue engineering at least requires sufficient osteoblast progenitors, efficient osteoinductive factors, and biocompatible scaffolding materials. We have demonstrated that BMP9 is one of the most potent factors in inducing osteogenic differentiation of mesenchymal progenitors. To facilitate the potential use of cell-based BMP9 gene therapy for bone regeneration, we characterize the in vivo osteoconductive activities and bone regeneration potential of three clinically used scaffold materials, type I collagen sponge, hydroxyapatite-tricalcium phosphate (HA-TCP), and demineralized bone matrix (DBM), using BMP9-expressing C2C12 osteoblastic progenitor cells. We find that recombinant adenovirus-mediated BMP9 expression effectively induces osteogenic differentiation in C2C12 cells. Although direct subcutaneous injection of BMP9-transduced C2C12 cells forms ectopic bony masses, subcutaneous implantation of BMP9-expressing C2C12 cells with collagen sponge or HA-TCP scaffold yields the most robust and mature cancellous bone formation, whereas the DBM carrier group forms no or minimal bone masses. Our results suggest that collagen sponge and HA-TCP scaffold carriers may provide more cell-friendly environment to support the survival, propagation, and ultimately differentiation of BMP9-expressing progenitor cells. This line of investigation should provide important experimental evidence for further preclinical studies in BMP9-mediated cell-based approach to bone tissue engineering.

Indexed as

Bone RegenerationTransduction, GeneticAnimalsCalcium PhosphatesCell DifferentiationChoristomaCollagen Type IDurapatiteGrowth Differentiation Factor 2HEK293 CellsHumansMaleMesenchymal Stem CellsMice, NudeOsteoblastsOsteogenesisCalcium PhosphatesCollagen Type IDurapatiteGrowth Differentiation Factor 2tricalcium phosphate

Identifiers

PMID24133046
PMCPMC4476251
OpenAlexW2155466257

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.