Evidence map›Paper›PMID 19494148›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2009

Early postnatal proteolipid promoter-expressing progenitors produce multilineage cells in vivo.

Fuzheng Guo, Joyce Ma, Erica McCauley, Peter Bannerman, David Pleasure

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed
5.3field-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

86 citing papers in PubMed, 132 citations in OpenAlex.

  1. Article
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  4. Review
  5. Article
  6. Recombinant Erythropoietin Induces Oligodendrocyte Progenitor Cell Proliferation After Traumatic Brain Injury and Delayed Hypoxemia.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Article
  7. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  8. Article
  9. Article
  10. Review
  11. Frontiers in cellular neuroscience · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

26 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

5 authors at 1 institution in 1 country.

Fuzheng GuoInstitute for Pediatric Regenerative Medicine, University of California, Davis, School of Medicine, Sacramento, California 95817, USA.
Joyce Ma
Erica McCauley
Peter Bannerman
David Pleasure
University of California, Davis · US

Funding

OLIGODENDROGLIAL PROLIFERATION AND DIFFERENTIATIONR01NS025044 · NINDS · UNIVERSITY OF CALIFORNIA DAVIS · PI PLEASURE, DAVID E. · 1987 to 2011
$3.9M
NINDS NIH HHS R01 NS025044
6 · The paper itself

Abstract

Proteolipid promoter (plp promoter) activity in the newborn mouse CNS is restricted to NG2-expressing oligodendroglial progenitor cells and oligodendrocytes. There are two populations of NG2 progenitors based on their plp promoter expression. Whereas the general population of NG2 progenitors has been shown to be multipotent in vitro and after transplantation, it is not known whether the subpopulation of plp promoter-expressing NG2 progenitors [i.e., plp promoter-expressing NG2 progenitors (PPEPs)] has the potential to generate multilineage cells during normal development in vivo. We addressed this issue by fate mapping Plp-Cre-ER(T2)/Rosa26-EYFP (PCE/R) double-transgenic mice, which carried an inducible Cre gene under the control of the plp promoter. Expression of the enhanced yellow fluorescent protein (EYFP) reporter gene in PPEPs was elicited by administering tamoxifen to postnatal day 7 PCE/R mice. We have demonstrated that early postnatal PPEPs, which had been thought to be restricted to the oligodendroglial lineage, also unexpectedly gave rise to a subset of immature, postmitotic, protoplasmic astrocytes in the gray matter of the spinal cord and ventral forebrain, but not in white matter. Furthermore, these PPEPs also gave rise to small numbers of immature, DCX (doublecortin)-negative neurons in the ventral forebrain, dorsal cerebral cortex, and hippocampus. EYFP-labeled representatives of each of these lineages survived to adulthood. These findings indicate that there are regional differences in the fates of neonatal PPEPs, which are multipotent in vivo, giving rise to oligodendrocytes, astrocytes, and neurons.

Indexed as

2',3'-Cyclic-Nucleotide PhosphodiesterasesAnimalsAnimals, NewbornAntigensAstrocytesBacterial ProteinsBrainBromodeoxyuridineCell DifferentiationCell ProliferationChondroitin Sulfate Proteoglycan 4Doublecortin Domain ProteinsDoublecortin ProteinEstrogen AntagonistsGene ExpressionImmediate-Early Proteins2',3'-Cyclic-Nucleotide PhosphodiesterasesAntigensBacterial ProteinsBromodeoxyuridineChondroitin Sulfate Proteoglycan 4Cre recombinaseDcx protein, mouseDoublecortin Domain ProteinsDoublecortin ProteinEstrogen AntagonistsGt(ROSA)26Sor non-coding RNA, mouseImmediate-Early ProteinsIntegrasesLuminescent ProteinsMicrotubule-Associated ProteinsNerve Tissue ProteinsNeuropeptidesProteinsProteoglycansProteolipidsRas-like protein, mouseRepressor ProteinsRNA, UntranslatedTamoxifenyellow fluorescent protein, Bacteria

Identifiers

PMID19494148
PMCPMC2717630
OpenAlexW2014827000

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.