Evidence map›Paper›PMID 20564220›Full record

ArticleJournal of cellular biochemistry2010

Recent advances in understanding the mechanisms of osteoclast precursor fusion.

Merry Jo Oursler

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular biochemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
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  10. Ostm1 from Mouse to Human: Insights into Osteoclast Maturation.International journal of molecular sciences · 2020
    Review
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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

1 author at 1 institution in 1 country.

Merry Jo OurslerRobert and Arlene Kogod Center on Aging, Endocrine Research Unit, Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota 55905, USA. oursler.merryjo@mayo.edu
Mayo Clinic in Arizona · US

Funding

SEX STEROIDS, GROWTH FACTORS, &BONE CELL FUNCTIONP01AG004875 · NIA · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 1985 to 2019
$30.8M
The Role Of Osteoclast PODXL, A Mediator Of Cell Adhesion, In Bone MetabolismR01DK091146 · NIDDK · MAYO CLINIC ROCHESTER · PI OURSLER, MERRY JO · 2010 to 2014
$1.6M
ROLE OF TGF-B INDUCIBLE EARLY GENE IN OSTEOCLASTOGENESISR01AR052004 · NIAMS · MAYO CLINIC ROCHESTER · PI OURSLER, MERRY JO · 2006 to 2010
$1.6M
NIAMS NIH HHS R01 AR052004NIAMS NIH HHS R01 AR52004NIA NIH HHS P01 AG004875NIDDK NIH HHS R01 DK091146
6 · The paper itself

Abstract

Bone marrow macrophages fuse on the bone surface to form multinucleated osteoclasts that then organize to efficiently resorb bone. Many, if not all, of the stages of macrophage fusion involve cytoskeletal components that reorganize the cells. Recruitment may involve chemotactic responses to bone matrix protein and calcium ion gradients and/or chemokine production by bone forming osteoblasts. The roles of integrins vary, depending on the particular subunits with some interfering with fusion and others having a participatory role. RANKL is essential for fusion and many identified modulators of fusion influence RANKL signaling pathways. Tetraspanins have been implicated in fusion of macrophages and myoblasts, but differences in impacts exist between these two cell types. Macrophage recruitment to apoptotic cells prior to their engulfment is driven by the exposed phospholipids on the external surface of the apoptotic cells and there is evidence that this same identification mechanism is employed in macrophage fusion. Because loss of cadherin or ADAM family members suppresses macrophage fusion, a crucial role for these membrane glycoproteins is evident. The Ig membrane glycoprotein superfamily members CD200 and MFR/SIRPalpha are involved in macrophage fusion, although their influences are unresolved. Differential screenings have identified the structurally related membrane proteins DC-STAMP and OC-STAMP as required components for fusion and the contributions to fusion remain active areas of investigation. While many of the key components involved in these processes have been identified, a great deal of work remains in resolving the precise processes involved and the interactions between key contributors to multinucleated osteoclast formation.

Indexed as

ADAM ProteinsAdaptor Proteins, Signal TransducingAnimalsAntigens, CDBone ResorptionCadherinsCell AdhesionCell FusionGiant CellsHumansIntegrinsMacrophagesMembrane ProteinsOsteoblastsOsteoclastsRANK LigandADAM ProteinsAdaptor Proteins, Signal TransducingAntigens, CDantigens, CD200CadherinsDCSTAMP protein, humanIntegrinsMembrane ProteinsOCSTAMP protein, humanRANK Ligand

Identifiers

PMID20564220
PMCPMC2913389
OpenAlexW1998093175

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.