Evidence map›Paper›PMID 24367913›Full record

ArticleASN neuro2014

PDGF-responsive progenitors persist in the subventricular zone across the lifespan.

Lisamarie Moore, Jennifer M Bain, Ji Meng Loh, Steven W Levison

Abstract read
In one paragraph

Article in ASN neuro, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Can Parkinson's disease be cured by stimulating neurogenesis?The Journal of clinical investigation · 2015
    Article
  12. 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

4 authors.

Lisamarie Moore
Jennifer M Bain
Ji Meng Loh§New Jersey Institute of Technology, Department of Mathematics, Newark, NJ 07102, U.S.A.
Steven W Levison

Funding

Neural Stem Cell Responses to Perinatal Brain DamageR01MH059950 · NIMH · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI LEVISON, STEVEN W · 1999 to 2008
$1.9M
Glial Dysgenesis in the Injured Developing BrainR01HD052064 · NICHD · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI LEVISON, STEVEN W · 2010 to 2013
$1.4M
The PDGF alpha neural progenitor cells of the subventricular zone contributes toF31NS076269 · NINDS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI MOORE, LISAMARIE · 2012 to 2014
$156k
The role of VEGF in neonatal rat brain after perinatal hypoxic-ischemic damageF31NS062629 · NINDS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI BAIN, JENNIFER M. · 2008 to 2008
$28k
NICHD NIH HHS HD052064NIMH NIH HHS MH59950NINDS NIH HHS 1F31NS062629NINDS NIH HHS 1F31NS076269NINDS NIH HHS F31 NS076269
6 · The paper itself

Abstract

The SVZ (subventricular zone) contains neural stem cells and progenitors of various potentialities. Although initially parsed into A, B, and C cells, this germinal zone is comprised of a significantly more diverse population of cells. Here, we characterized a subset of postnatal PRPs (PDGF-AA-responsive precursors) that express functional PDGFα and β receptors from birth to adulthood. When grown in PDGF-AA, dissociated neonatal rat SVZ cells divided to produce non-adherent clusters of progeny. Unlike the self-renewing EGF/FGF-2-responsive precursors that produce neurospheres, these PRPs failed to self-renew after three passages; therefore, we refer to the colonies they produce as spheroids. Upon differentiation these spheroids could produce neurons, type 1 astrocytes and oligodendrocytes. When maintained in medium supplemented with BMP-4 they also produced type 2 astrocytes. Using lineage tracing methods, it became evident that there were multiple types of PRPs, including a subset that could produce neurons, oligodendrocytes, and type 1 and type 2 astrocytes; thus some of these PRPs represent a unique population of precursors that are quatropotential. Spheroids also could be generated from the newborn neocortex and they had the same potentiality as those from the SVZ. By contrast, the adult neocortex produced less than 20% of the numbers of spheroids than the adult SVZ and spheroids from the adult neocortex only differentiated into glial cells. Interestingly, SVZ spheroid producing capacity diminished only slightly from birth to adulthood. Altogether these data demonstrate that there are PRPs that persist in the SVZ that includes a unique population of quatropotential PRPs.

Indexed as

AnimalsAnimals, NewbornAstrocytesBone Morphogenetic Protein 4Cell DifferentiationCell LineageCells, CulturedEpidermal Growth FactorFibroblast Growth Factor 2Lateral VentriclesNeocortexNeural Stem CellsNeurogenesisNeuronsOligodendrogliaPlatelet-Derived Growth FactorBmp4 protein, ratBone Morphogenetic Protein 4Epidermal Growth FactorFibroblast Growth Factor 2Platelet-Derived Growth Factorplatelet-derived growth factor AProto-Oncogene Proteins c-sis

Identifiers

PMID24367913
PMCPMC3917572

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Registered trials

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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.