Evidence map›Paper›PMID 19269977›Full record

ArticleThe Journal of biological chemistry2009

Regulated proteolysis of nonmuscle myosin IIA stimulates osteoclast fusion.

Brooke K McMichael, Robert B Wysolmerski, Beth S Lee

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
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  4. Review
  5. Article
  6. Osteoclast Multinucleation: Review of Current Literature.International journal of molecular sciences · 2020
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Genetic basis of cell-cell fusion mechanisms.Trends in genetics : TIG · 2013
    Review
  15. Paxillin contracts the osteoclast cytoskeleton.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2012
    Article
  16. An essential role for the association of CD47 to SHPS-1 in skeletal remodeling.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2011
    Article
  17. Quantitative proteomic analysis of dexamethasone-induced effects on osteoblast differentiation, proliferation, and apoptosis in MC3T3-E1 cells using SILAC.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2011
    Article
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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

3 authors at 2 institutions in 1 country.

Brooke K McMichaelDepartment of Physiology and Cell Biology, The Ohio State University College of Medicine, Columbus, Ohio 43210, USA.
Robert B Wysolmerski
Beth S Lee
The Ohio State University · USWest Virginia University · US

Funding

THE ROLE OF HEF1 PROTEIN IN INVASION OF METASTATIC BREAST CANCERP20RR016440 · NCRR · WEST VIRGINIA UNIVERSITY · PI CUFF, CHRISTOPHER F · 2001 to 2010
$22.8M
TRANSCRIPTIONAL CONTROL OF VACUOLAR H+-ATPASE EXPRESSIONR01DK052131 · NIDDK · WASHINGTON UNIVERSITY · PI LEE, BETH S. · 1997 to 2009
$2.7M
REGULATION OF ENDOTHELIAL CELL ISOMETRIC TENSIONR01HL045788 · NHLBI · WEST VIRGINIA UNIVERSITY · PI WYSOLMERSKI, ROBERT B. · 1996 to 2006
$1.9M
DYNAMICS OF THE ACTIN CYTOSKELETON IN OSTEOCLASTSR01AR051515 · NIAMS · OHIO STATE UNIVERSITY · PI LEE, BETH S. · 2006 to 2009
$1.0M
ENDOTHELIAL CELL RETRACTION AND EDEMA OF ARDSR29HL045788 · NHLBI · SAINT LOUIS UNIVERSITY · PI WYSOLMERSKI, ROBERT B. · 1991 to 1995
–
NCRR NIH HHS P20-RR16440NHLBI NIH HHS HL-45788NIAMS NIH HHS AR051515NIDDK NIH HHS DK052131
6 · The paper itself

Abstract

The nonmuscle myosin IIA heavy chain (Myh9) is strongly associated with adhesion structures of osteoclasts. In this study, we demonstrate that during osteoclastogenesis, myosin IIA heavy chain levels are temporarily suppressed, an event that stimulates the onset of cell fusion. This suppression is not mediated by changes in mRNA or translational levels but instead is due to a temporary increase in the rate of myosin IIA degradation. Intracellular activity of cathepsin B is significantly enhanced at the onset of osteoclast precursor fusion, and specific inhibition of its activity prevents myosin IIA degradation. Further, treatment of normal cells with cathepsin B inhibitors during the differentiation process reduces cell fusion and bone resorption capacity, whereas overexpression of cathepsin B enhances fusion. Ongoing suppression of the myosin IIA heavy chain via RNA interference results in formation of large osteoclasts with significantly increased numbers of nuclei, whereas overexpression of myosin IIA results in less osteoclast fusion. Increased multinucleation caused by myosin IIA suppression does not require RANKL. Further, knockdown of myosin IIA enhances cell spreading and lessens motility. These data taken together strongly suggest that base-line expression of nonmuscle myosin IIA inhibits osteoclast precursor fusion and that a temporary, cathepsin B-mediated decrease in myosin IIA levels triggers precursor fusion during osteoclastogenesis.

Indexed as

AnimalsCathepsin BCell AdhesionCell FusionCell LineCell MovementCell NucleusGene Knockout TechniquesMiceMyosin Heavy ChainsNonmuscle Myosin Type IIAOsteoclastsRANK LigandCathepsin BCtsb protein, mouseMyh9 protein, mouseMyosin Heavy ChainsNonmuscle Myosin Type IIARANK LigandTnfsf11 protein, mouse

Identifiers

PMID19269977
PMCPMC2673295
OpenAlexW2049268865

What OpenQuestion holds

Textmetadata
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.