Evidence map›Paper›PMID 10359570›Full record

ArticleThe Journal of clinical investigation1999

Annexin II increases osteoclast formation by stimulating the proliferation of osteoclast precursors in human marrow cultures.

C Menaa, R D Devlin, S V Reddy, Y Gazitt, S J Choi, G D Roodman

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
1.8field-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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 107 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Hypoxia favors the generation of human plasma cells.Cell cycle (Georgetown, Tex.) · 2017
    Article
  14. Article
  15. Article
  16. Distal convoluted tubule.Comprehensive Physiology · 2015
    Review
  17. Article
  18. Article
  19. Article
  20. Annexin A2 heterotetramer: structure and function.International journal of molecular sciences · 2013
    Article
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

6 authors at 2 institutions in 1 country.

C MenaaDepartment of Medicine/Hematology, University of Texas Health Science Center, San Antonio, Texas 78284, USA Audie Murphy Veterans Administration Hospital, San Antonio, Texas 78284, USA.
R D Devlin
S V Reddy
Y Gazitt
S J Choi
G D Roodman
The University of Texas Health Science Center at San Antonio · USPalmetto Hematology Oncology · US

Funding

TUMORS EFFECTS ON THE SKELETONP01CA040035 · NCI · VANDERBILT UNIVERSITY · PI SUN, LUZHE · 1985 to 2010
$11.0M
OSTEOCLASTS FROM TRANSGENIC MICER01AR041336 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI ROODMAN, GARSON DAVID · 1991 to 2009
$2.3M
DEVELOPMENTAL ASPECTS OF OSTEOCLAST FORMATION IN VITROR01AG013625 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI ROODMAN, GARSON DAVID · 1995 to 2005
$1.3M
PATHOBIOLOGY OF THE OSTEOCLAST IN PAGETS DISEASER01AR044603 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI ROODMAN, G DAVID · 1998 to 2002
$792k
NCI NIH HHS CA-40035NCI NIH HHS P01 CA040035NIAMS NIH HHS AR-44603NIAMS NIH HHS R01 AR041336NIAMS NIH HHS R01 AR044603NIA NIH HHS AG-13625NIA NIH HHS R01 AG013625
6 · The paper itself

Abstract

Annexin II (AXII), a calcium-dependent phospholipid-binding protein, has been recently found to be an osteoclast (OCL) stimulatory factor that is also secreted by OCLs. In vitro studies showed that AXII induced OCL formation and bone resorption. However, the mechanism of action by which AXII acts as a soluble extracellular protein to induce OCL formation is unknown. In this paper, we demonstrate that AXII gene expression is upregulated by 1,25-dihydroxyvitamin D3 [1, 25-(OH)2D3] and that addition of AXII significantly increased OCL-like multinucleated cell formation. Time-course studies suggested that AXII acted on the proliferative stage of OCL precursors and that AXII increased thymidine incorporation in OCL precursors. Moreover, AXII enhanced the growth of CFU-GM, the earliest identifiable OCL precursor, when bone marrow cultures were treated with low concentrations of GM-CSF. This capacity of AXII to induce OCL precursor proliferation was due to induction of GM-CSF expression, because the addition of neutralizing antibodies to GM-CSF blocked the stimulatory effect of AXII on OCL formation. RT-PCR analysis using RNA from highly purified subpopulations of marrow cells demonstrated that T cells, especially CD4(+) T cells, produced GM-CSF in response to AXII. Furthermore, FACS(R) analysis of T-cell subpopulations treated with fluorescein-labeled AXII suggested that the CD4(+), but not CD8(+), subpopulation of T cells express an AXII receptor. Taken together, these data suggest that AXII stimulates OCL formation by activating T cells through a putative receptor to secrete GM-CSF. GM-CSF then expands the OCL precursor pool to enhance OCL formation.

Indexed as

Annexin A2Bone Marrow CellsCell DifferentiationCell DivisionGranulocyte-Macrophage Colony-Stimulating FactorHumansNeutralization TestsOsteoclastsRNA, MessengerStem CellsStromal CellsT-LymphocytesAnnexin A2Granulocyte-Macrophage Colony-Stimulating FactorRNA, Messenger

Identifiers

PMID10359570
PMCPMC408373
OpenAlexW2141990015

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.