Evidence map›Paper›PMID 23073844›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2012

The skeletal site-specific role of connective tissue growth factor in prenatal osteogenesis.

Alex G Lambi, Talia L Pankratz, Christina Mundy, Maureen Gannon, Mary F Barbe, Joan T Richtsmeier, Steven N Popoff

Open access · bronzeAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2012. 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
0.8field-weighted citation impact, top 30% 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, 42 citations in OpenAlex.

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  17. The pivotal role of CCN2 in mammalian palatogenesis.Journal of cell communication and signaling · 2017
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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 3 institutions in 1 country.

Alex G LambiDepartment of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.
Talia L Pankratz
Christina Mundy
Maureen Gannon
Mary F Barbe
Joan T Richtsmeier
Steven N Popoff
Temple University · USPennsylvania State University · USVanderbilt University Medical Center · US

Funding

THE ROLE OF CTGF IN OSTEOBLAST DEVELOPMENT AND FUNCTIONR01AR047432 · NIAMS · TEMPLE UNIV OF THE COMMONWEALTH · PI POPOFF, STEVEN N. · 2002 to 2012
$3.1M
Midface and Upper Airway in CraniosynostosisR01DE022988 · NIDCR · PENNSYLVANIA STATE UNIVERSITY, THE · PI JABS, ETHYLIN WANG, RICHTSMEIER, JOAN THERESE · 2012 to 2016
$3.1M
PHENOGENETICS OF SKULL AND BRAIN INTEGRATION IN CRANIOSYNOSTOSISR01DE018500 · NIDCR · PENNSYLVANIA STATE UNIVERSITY, THE · PI RICHTSMEIER, JOAN THERESE · 2008 to 2012
$2.8M
High-resolution ex vivo micro-computerized tomography systemS10RR026727 · NCRR · TEMPLE UNIV OF THE COMMONWEALTH · PI BARBE, MARY F · 2010 to 2010
$308k
NIAMS NIH HHS R01 AR047432NIDCR NIH HHS 3R01DE018500-02S1NIDCR NIH HHS R01 DE018500NIDCR NIH HHS R01DE018500NIDCR NIH HHS R01 DE022988
6 · The paper itself

Abstract

backgroundConnective tissue growth factor (CTGF/CCN2) is a matricellular protein that is highly expressed during bone development. Mice with global CTGF ablation (knockout, KO) have multiple skeletal dysmorphisms and perinatal lethality. A quantitative analysis of the bone phenotype has not been conducted.

resultsWe demonstrated skeletal site-specific changes in growth plate organization, bone microarchitecture, and shape and gene expression levels in CTGF KO compared with wild-type mice. Growth plate malformations included reduced proliferation zone and increased hypertrophic zone lengths. Appendicular skeletal sites demonstrated decreased metaphyseal trabecular bone, while having increased mid-diaphyseal bone and osteogenic expression markers. Axial skeletal analysis showed decreased bone in caudal vertebral bodies, mandibles, and parietal bones in CTGF KO mice, with decreased expression of osteogenic markers. Analysis of skull phenotypes demonstrated global and regional differences in CTGF KO skull shape resulting from allometric (size-based) and nonallometric shape changes. Localized differences in skull morphology included increased skull width and decreased skull length. Dysregulation of the transforming growth factor-β-CTGF axis coupled with unique morphologic traits provides a potential mechanistic explanation for the skull phenotype.

conclusionsWe present novel data on a skeletal phenotype in CTGF KO mice, in which ablation of CTGF causes site-specific aberrations in bone formation.

Indexed as

Cell ProliferationAnimalsAntigens, DifferentiationConnective Tissue Growth FactorGrowth PlateMiceMice, KnockoutOrgan SpecificityOsteogenesisSkullSpineAntigens, DifferentiationCCN2 protein, mouseConnective Tissue Growth Factor

Identifiers

PMID23073844
PMCPMC3752831
OpenAlexW1981501451

What OpenQuestion holds

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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.