Evidence map›Paper›PMID 21898543›Full record

ArticleJournal of cellular biochemistry2012

Erythropoietin mediated bone formation is regulated by mTOR signaling.

Jinkoo Kim, Younghun Jung, Hongli Sun, Jeena Joseph, Anjali Mishra, Yusuke Shiozawa, Jingcheng Wang, Paul H Krebsbach, Russell S Taichman

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cellular biochemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

69 citing papers in PubMed, 116 citations in OpenAlex.

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  14. Hypoxia-Inducible Factors Signaling in Osteogenesis and Skeletal Repair.International journal of molecular sciences · 2022
    Review
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9 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

9 authors at 1 institution in 1 country.

Jinkoo KimDepartment of Periodontics and Oral Medicine, University of Michigan School of Dentistry, Ann Arbor, Michigan 48109-1078, USA.
Younghun Jung
Hongli Sun
Jeena Joseph
Anjali Mishra
Yusuke Shiozawa
Jingcheng Wang
Paul H Krebsbach
Russell S Taichman
University of Michigan–Ann Arbor · US

Funding

Tumor microvesicle-mediated modulation of the bone microenvironmentP01CA093900 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PIENTA, KENNETH J. · 2004 to 2024
$29.6M
FunctionalCharacterization of the Stem Cell NicheR01DK082481 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KREBSBACH, PAUL HUGO, TAICHMAN, RUSSELL S · 2009 to 2012
$1.4M
BONE MARROW STROMAL CELLS FOR SKELETAL REGENERATIONR01DE013835 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KREBSBACH, PAUL H · 2001 to 2005
$1.3M
The Use of Erythropoietin to Reprogram Oral and Craniofacial Stem CellsRC1DE020721 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KOHN, DAVID H., KREBSBACH, PAUL HUGO · 2009 to 2010
$971k
AXII in the Multiple Myeloma Bone MicroenvironmentR21CA141426 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ROODMAN, GARSON DAVID · 2010 to 2011
$324k
NCI NIH HHS CA093900NCI NIH HHS CA141426NCI NIH HHS P01 CA093900NCI NIH HHS R21 CA141426NIDCR NIH HHS 1RC1DE020721NIDCR NIH HHS DE020721NIDCR NIH HHS R01 DE013835NIDCR NIH HHS RC1 DE020721NIDDK NIH HHS DK082481NIDDK NIH HHS R01 DK082481
6 · The paper itself

Abstract

The role of erythropoietin (Epo) and Epo/Epo receptor (EpoR) signaling pathways for production of red blood cells are well established. However, little is known about Epo/EpoR signaling in non-hematopoietic cells. Recently, we demonstrated that Epo activates JAK/STAT signaling in hematopoietic stem cells (HSCs), leading to the production of bone morphogenetic protein 2 (BMP2) and bone formation and that Epo also directly activates mesenchymal cells to form osteoblasts in vitro. In this study, we investigated the effects of mTOR signaling on Epo-mediated osteoblastogenesis and osteoclastogenesis. We found that mTOR inhibition by rapamycin blocks Epo-dependent and -independent osteoblastic phenotypes in human bone marrow stromal cells (hBMSCs) and ST2 cells, respectively. Furthermore, we found that rapamycin inhibits Epo-dependent and -independent osteoclastogenesis in mouse bone marrow mononuclear cells and Raw264.7 cells. Finally, we demonstrated that Epo increases NFATc1 expression and decreases cathepsin K expression in an mTOR-independent manner, resulting in an increase of osteoclast numbers and a decrease in resorption activity. Taken together, these results strongly indicate that mTOR signaling plays an important role in Epo-mediated bone homeostasis.

Indexed as

AnimalsBone and BonesBone DevelopmentCathepsin KCell DifferentiationCell LineCell ProliferationErythropoietinHumansMiceNFATC Transcription FactorsOsteoblastsOsteoclastsOsteogenesisReceptors, ErythropoietinSignal TransductionCathepsin KErythropoietinMTOR protein, humanNFATC1 protein, humanNFATC Transcription FactorsReceptors, ErythropoietinSirolimusTOR Serine-Threonine Kinases

Identifiers

PMID21898543
PMCPMC3237787
OpenAlexW2108809192

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.