Evidence map›Paper›PMID 23266958›Full record

ArticleThe Journal of cell biology2012

Plasma membrane calcium ATPase regulates bone mass by fine-tuning osteoclast differentiation and survival.

Hyung Joon Kim, Vikram Prasad, Seok-Won Hyung, Zang Hee Lee, Sang-Won Lee, Aditi Bhargava, David Pearce, Youngkyun Lee, Hong-Hee Kim

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
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  9. Article
  10. Sestrin2 Regulates Osteoclastogenesis via the p62-TRAF6 Interaction.Frontiers in cell and developmental biology · 2021
    Article
  11. Membrane Transport Proteins in Osteoclasts: The Ins and Outs.Frontiers in cell and developmental biology · 2021
    Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Primary Active CaCold Spring Harbor perspectives in biology · 2020
    Review
  17. Article
  18. Article
  19. Article
  20. 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

9 authors at 5 institutions in 2 countries.

Hyung Joon KimDepartment of Cell and Developmental Biology, BK21 Program and Dental Research Institute, Seoul National University, Seoul 110-749, Korea.
Vikram Prasad
Seok-Won Hyung
Zang Hee Lee
Sang-Won Lee
Aditi Bhargava
David Pearce
Youngkyun Lee
Hong-Hee Kim
Seoul National University · KRKorea University · KRUniversity of California, San Francisco · USKyungpook National University · KRUniversity of Cincinnati Medical Center · US

Funding

Mouse Models for Ion Homeostasis Defects in HeartR01HL061974 · NHLBI · UNIVERSITY OF CINCINNATI · PI SHULL, GARY EDWARD · 1999 to 2010
$5.1M
Regulation and Function of Urocortins and their ReceptorsR01DK080787 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BHARGAVA, ADITI · 2009 to 2013
$2.2M
NHLBI NIH HHS HL061974NHLBI NIH HHS R01 HL061974
6 · The paper itself

Abstract

The precise regulation of Ca(2+) dynamics is crucial for proper differentiation and function of osteoclasts. Here we show the involvement of plasma membrane Ca(2+) ATPase (PMCA) isoforms 1 and 4 in osteoclastogenesis. In immature/undifferentiated cells, PMCAs inhibited receptor activator of NF-κB ligand-induced Ca(2+) oscillations and osteoclast differentiation in vitro. Interestingly, nuclear factor of activated T cell c1 (NFATc1) directly stimulated PMCA transcription, whereas the PMCA-mediated Ca(2+) efflux prevented NFATc1 activation, forming a negative regulatory loop. PMCA4 also had an anti-osteoclastogenic effect by reducing NO, which facilitates preosteoclast fusion. In addition to their role in immature cells, increased expression of PMCAs in mature osteoclasts prevented osteoclast apoptosis both in vitro and in vivo. Mice heterozygous for PMCA1 or null for PMCA4 showed an osteopenic phenotype with more osteoclasts on bone surface. Furthermore, PMCA4 expression levels correlated with peak bone mass in premenopausal women. Thus, our results suggest that PMCAs play important roles for the regulation of bone homeostasis in both mice and humans by modulating Ca(2+) signaling in osteoclasts.

Indexed as

Cell DifferentiationCell SurvivalAdultAmino Acid SequenceAnimalsApoptosisBone DensityCalcium SignalingCell FusionCells, CulturedFemaleFemurHumansMaleMiceMice, 129 StrainATP2B1 protein, humanATP2B4 protein, humanNFATC Transcription FactorsNitric OxidePlasma Membrane Calcium-Transporting ATPasesProtein IsoformsRANK Ligand

Identifiers

PMID23266958
PMCPMC3529522
OpenAlexW2044489236

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.