Evidence map›Paper›PMID 19440205›Full record

ArticleThe EMBO journal2009

Transcription factor C/EBPbeta isoform ratio regulates osteoclastogenesis through MafB.

Jeske J Smink, Valérie Bégay, Ton Schoenmaker, Esta Sterneck, Teun J de Vries, Achim Leutz

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

71 citing papers in PubMed, 1 synthesis or guideline pooled it, 130 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Transcription-based comparison ofMicrobiology spectrum · 2026
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  6. Autophagy: regulating the seesaw of bone-fat balance.Frontiers in cell and developmental biology · 2025
    Review
  7. Article
  8. Review
  9. Transcription factor C/EBPα is required for the development of Ly6CProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. TLR or NOD receptor signaling skews monocyte fate decision via distinct mechanisms driven by mTOR and miR-155.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. Relationships betweenComparative medicine · 2021
    Article
  18. Article
  19. Article
  20. Article

11 more citing papers are in PubMed but not listed here.

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 3 institutions in 3 countries.

Jeske J SminkMax Delbrueck Center for Molecular Medicine, Berlin, Germany.
Valérie Bégay
Ton Schoenmaker
Esta Sterneck
Teun J de Vries
Achim Leutz
Max Delbrück Center · DEVrije Universiteit Amsterdam · NLNational Cancer Institute · US

Funding

Molecular Mechanisms Regulating Mouse Mammary Gland and Human Breast Tumor CellsZIABC010307 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI STERNECK, GISELA · 2009 to 2025
$22.1M
Molecular Mechanisms Regulating Mouse Mammary Gland and Human Breast Tumor CellsZ01BC010307 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI STERNECK, ESTA · 1999 to 2008
$1.8M
6 · The paper itself

Abstract

Disequilibrium between bone-forming osteoblasts and bone-resorbing osteoclasts is central to many bone diseases. Here, we show that dysregulated expression of translationally controlled isoforms of CCAAT/enhancer-binding protein beta (C/EBPbeta) differentially affect bone mass. Alternative translation initiation that is controlled by the mammalian target of rapamycin (mTOR) pathway generates long transactivating (LAP(*), LAP) and a short repressive (LIP) isoforms from a single C/EBPbeta transcript. Rapamycin, an inhibitor of mTOR signalling increases the ratio of LAP over LIP and inhibits osteoclastogenesis in wild type (WT) but not in C/EBPbeta null (c/ebpbeta(-/-)) or in LIP knock-in (L/L) osteoclast precursors. C/EBPbeta mutant mouse strains exhibit increased bone resorption and attenuated expression of MafB, a negative regulator of osteoclastogenesis. Ectopic expression of LAP and LIP in monocytes differentially affect the MafB promoter activity, MafB gene expression and dramatically affect osteoclastogenesis. These data show that mTOR regulates osteoclast formation by modulating the C/EBPbeta isoform ratio, which in turn affects osteoclastogenesis by regulating MafB expression.

Indexed as

Cell DifferentiationAnimalsBone and BonesCCAAT-Enhancer-Binding Protein-betaGene Knock-In TechniquesMafB Transcription FactorMiceMice, Mutant StrainsModels, BiologicalMutationOrgan SizeOsteoblastsOsteoclastsProtein IsoformsProtein KinasesTOR Serine-Threonine KinasesCCAAT-Enhancer-Binding Protein-betaMafb protein, mouseMafB Transcription FactormTOR protein, mouseProtein IsoformsProtein KinasesTOR Serine-Threonine Kinases

Identifiers

PMID19440205
PMCPMC2685610
OpenAlexW2021284127

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.