Evidence map›Paper›PMID 25222280›Full record

ArticlePloS one2014

Impaired osteoblast differentiation in annexin A2- and -A5-deficient cells.

Damian C Genetos, Alice Wong, Thomas J Weber, Norman J Karin, Clare E Yellowley

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

29 citing papers in PubMed, 67 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Damian C GenetosDepartment of Anatomy, Physiology and Cell Biology, School of Veterinary Medicine, University of California Davis, Davis, CA, United States of America.
Alice WongDepartment of Anatomy, Physiology and Cell Biology, School of Veterinary Medicine, University of California Davis, Davis, CA, United States of America.
Thomas J WeberSystems Toxicology, Pacific Northwest National Laboratory, Richland, WA, United States of America.
Norman J KarinSystems Toxicology, Pacific Northwest National Laboratory, Richland, WA, United States of America.
Clare E YellowleyDepartment of Anatomy, Physiology and Cell Biology, School of Veterinary Medicine, University of California Davis, Davis, CA, United States of America.
University of California, Davis · USPacific Northwest National Laboratory · US

Funding

Regulation of sclerostin expression by hypoxia: A proposed mechanism to explain hR03AR057547 · NIAMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GENETOS, DAMIAN C · 2010 to 2012
$224k
NIAMS NIH HHS R03 AR057547
6 · The paper itself

Abstract

Annexins are a class of calcium-binding proteins with diverse functions in the regulation of lipid rafts, inflammation, fibrinolysis, transcriptional programming and ion transport. Within bone, they are well-characterized as components of mineralizing matrix vesicles, although little else is known as to their function during osteogenesis. We employed shRNA to generate annexin A2 (AnxA2)- or annexin A5 (AnxA5)-knockdown pre-osteoblasts, and determined whether proliferation or osteogenic differentiation was altered in knockdown cells, compared to pSiren (Si) controls. We report that DNA content, a marker of proliferation, was significantly reduced in both AnxA2 and AnxA5 knockdown cells. Alkaline phosphatase expression and activity were also suppressed in AnxA2- or AnxA5-knockdown after 14 days of culture. The pattern of osteogenic gene expression was altered in knockdown cells, with Col1a1 expressed more rapidly in knock-down cells, compared to pSiren. In contrast, Runx2, Ibsp, and Bglap all revealed decreased expression after 14 days of culture. In both AnxA2- and AnxA5-knockdown, interleukin-induced STAT6 signaling was markedly attenuated compared to pSiren controls. These data suggest that AnxA2 and AnxA5 can influence bone formation via regulation of osteoprogenitor proliferation, differentiation, and responsiveness to cytokines in addition to their well-studied function in matrix vesicles.

Indexed as

AnimalsAnnexin A2Annexin A5Cell DifferentiationCell ProliferationCollagen Type ICollagen Type I, alpha 1 ChainCore Binding Factor Alpha 1 SubunitGene Expression Regulation, DevelopmentalGene Knockdown TechniquesIntegrin-Binding SialoproteinMiceOsteoblastsOsteogenesisRNA, Small InterferingSignal TransductionAnnexin A2Annexin A5Collagen Type ICollagen Type I, alpha 1 ChainCore Binding Factor Alpha 1 SubunitIbsp protein, mouseIntegrin-Binding SialoproteinRNA, Small InterferingRunx2 protein, mouseSTAT6 Transcription Factor

Identifiers

PMID25222280
PMCPMC4164658
OpenAlexW2019071999

What OpenQuestion holds

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LicenceCC0
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.