Evidence map›Paper›PMID 28286238›Full record

ArticleBone2017

The role of the progressive ankylosis protein (ANK) in adipogenic/osteogenic fate decision of precursor cells.

Takeshi Minashima, Martin Quirno, You Jin Lee, Thorsten Kirsch

Abstract read
In one paragraph

Article in Bone, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 17 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

4 authors at 1 institution in 1 country.

Takeshi MinashimaMusculoskeletal Research Center, Department of Orthopaedic Surgery, New York University School of Medicine, NY, New York, United States.
Martin QuirnoMusculoskeletal Research Center, Department of Orthopaedic Surgery, New York University School of Medicine, NY, New York, United States.
You Jin LeeMusculoskeletal Research Center, Department of Orthopaedic Surgery, New York University School of Medicine, NY, New York, United States.
Thorsten KirschMusculoskeletal Research Center, Department of Orthopaedic Surgery, New York University School of Medicine, NY, New York, United States. Electronic address: thorsten.kirsch@nyumc.org.
New York University · US

Funding

Annexins and OsteoarthritisR01AR064186 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KIRSCH, THORSTEN · 2014 to 2018
$1.9M
NIAMS NIH HHS R01 AR064186
6 · The paper itself

Abstract

The progressive ankylosis protein (ANK) is a transmembrane protein that transports intracellular pyrophosphate (PPi) to the extracellular milieu. In this study we show increased fatty degeneration of the bone marrow of adult ank/ank mice, which lack a functional ANK protein. In addition, isolated bone marrow stromal cells (BMSCs) isolated from ank/ank mice showed a decreased proliferation rate and osteogenic differentiation potential, and an increased adipogenic differentiation potential compared to BMSCs isolated from wild type (WT) littermates. Wnt signaling pathway PCR array analysis revealed that Wnt ligands, Wnt receptors and Wnt signaling proteins that stimulate osteoblast differentiation were expressed at markedly lower levels in ank/ank BMSCs than in WT BMSCs. Lack of ANK function also resulted in impaired bone fracture healing, as indicated by a smaller callus formed and delayed bone formation in the callus site. Whereas 5weeks after fracture, the fractured bone in WT mice was further remodeled and restored to original shape, the fractured bone in ank/ank mice was not fully restored and remodeled to original shape. In conclusion, our study provides evidence that ANK plays a critical role in the adipogenic/osteogenic fate decision of adult mesenchymal precursor cells. ANK functions in precursor cells are required for osteogenic differentiation of these cells during adult bone homeostasis and repair, whereas lack of ANK functions favors adipogenic differentiation.

Indexed as

AdipocytesAdipogenesisAnimalsBone MarrowCell DifferentiationFemaleMaleMesenchymal Stem CellsMiceMice, Mutant StrainsOsteocytesOsteogenesisPhosphate Transport ProteinsReal-Time Polymerase Chain ReactionWnt Signaling PathwayX-Ray Microtomographyank protein, mousePhosphate Transport ProteinsAdipogenesisBone fracture healingOsteogenesisProgressive ankylosis protein (ANK)Wnt/β-catenin signaling

Identifiers

PMID28286238
PMCPMC5396059
OpenAlexW2592932705

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.