Evidence map›Paper›PMID 19417086›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2009

Erythropoietin signaling promotes transplanted progenitor cell survival.

Yi Jia, Renaud Warin, Xiaobing Yu, Reed Epstein, Constance Tom Noguchi

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

19 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
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  10. Erythropoietin action in stress response, tissue maintenance and metabolism.International journal of molecular sciences · 2014
    Review
  11. Article
  12. Review
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  14. Article
  15. Article
  16. Article
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  18. Endogenous erythropoietin signaling facilitates skeletal muscle repair and recovery following pharmacologically induced damage.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2012
    Article
  19. 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

5 authors at 2 institutions in 1 country.

Yi JiaMolecular Medicine Branch, NIDDK, National Institutes of Health, Bethesda, MD 20892-1822, USA.
Renaud Warin
Xiaobing Yu
Reed Epstein
Constance Tom Noguchi
National Institute of Diabetes and Digestive and Kidney Diseases · USNational Institutes of Health · US

Funding

Globin Gene Expression And Treatment Of Sickle Cell AnemiaZIADK025021 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI NOGUCHI, CONSTANCE · 2009 to 2025
$6.3M
Role of erythropoietin in skeletal muscle and bone maintenance and repairZIADK025103 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI NOGUCHI, CONSTANCE · 2009 to 2015
$2.2M
Role of erythropoietin in muscle maintenance and repairZ01DK025103 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI NOGUCHI, CONSTANCE · 2007 to 2008
$511k
Intramural NIH HHS
6 · The paper itself

Abstract

We examine the potential for erythropoietin signaling to promote donor cell survival in a model of myoblast transplantation. Expression of a truncated erythropoietin receptor in hematopoietic stem cells has been shown to promote selective engraftment in mice. We previously demonstrated expression of endogenous erythropoietin receptor on murine myoblasts, and erythropoietin treatment can stimulate myoblast proliferation and delay differentiation. Here, we report that enhanced erythropoietin receptor expression, as well as exogenous erythropoietin treatment in myoblasts, provided a survival advantage and protection against apoptosis under serum-starvation conditions. When cultured in differentiation medium, expression of the myogenic regulatory proteins shifted toward early differentiation with increased erythropoietin receptor. Expression of early myogenic differentiation proteins Myf-5 and MyoD increased, while later stage protein myogenin decreased. Transplantation of C2C12 myoblasts overexpressing truncated erythropoietin receptor showed more transplanted cell incorporation into muscle fibers in muscular dystrophy mdx mice. These cells also restored dystrophin protein expression in mdx mice at 6 wk after cell treatment that was further increased with exogenous erythropoietin administration. In summary, enhanced erythropoietin receptor expression promotes transplanted cell survival in a mouse model for myoblast transplantation and provides dystrophin expression in mice with muscular dystrophy.

Indexed as

AnimalsCells, CulturedCell SurvivalDystrophinErythropoietinMiceMuscular DystrophiesMyoblastsReceptors, ErythropoietinSignal TransductionStem CellsStem Cell TransplantationDystrophinErythropoietinReceptors, Erythropoietin

Identifiers

PMID19417086
PMCPMC2735366
OpenAlexW2014434110

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.