Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
19
pubmed:dateCreated
2007-4-26
pubmed:abstractText
An instability of the mature cell phenotype is thought to participate to the formation of gliomas, primary brain tumors deriving from astrocytes and/or neural stem cells. Transforming growth factor alpha (TGFalpha) is an erbB1 ligand overexpressed in the earliest stages of gliomas, and exerts trophic effects on gliomal cells and astrocytes. Here, we questioned whether prolonged TGFalpha exposure affects the stability of the normal mature astrocyte phenotype. We first developed astrocyte cultures devoid of residual neural stem cells or progenitors. We demonstrate that days of TGFalpha treatment result in the functional conversion of a population of mature astrocytes into radial glial cells, a population of neural progenitors. TGFalpha-generated radial glial cells support embryonic neurons migration, and give birth to cells of the neuronal lineage, expressing neuronal markers and the electrophysiological properties of neuroblasts. Lengthening TGFalpha treatment to months results in the delayed appearance of cells with neural stem cells properties: they form floating cellular spheres that are self-renewing, can be clonally derived from a single cell and differentiated into cells of the neuronal lineage. This study uncovers a novel population of mature astrocytes capable, in response to a single epigenetic factor, to regress progressively into a neural stem-like cell stage via an intermediate progenitor stage.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0950-9232
pubmed:author
pubmed:issnType
Print
pubmed:day
26
pubmed:volume
26
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2695-706
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:17057735-Animals, pubmed-meshheading:17057735-Astrocytes, pubmed-meshheading:17057735-Cell Differentiation, pubmed-meshheading:17057735-Cell Lineage, pubmed-meshheading:17057735-Cell Movement, pubmed-meshheading:17057735-Cells, Cultured, pubmed-meshheading:17057735-Electrophysiology, pubmed-meshheading:17057735-Embryo, Mammalian, pubmed-meshheading:17057735-Female, pubmed-meshheading:17057735-Fetus, pubmed-meshheading:17057735-Humans, pubmed-meshheading:17057735-Immunoblotting, pubmed-meshheading:17057735-Immunoprecipitation, pubmed-meshheading:17057735-Mice, pubmed-meshheading:17057735-Mice, Inbred C57BL, pubmed-meshheading:17057735-Neuroglia, pubmed-meshheading:17057735-Neurons, pubmed-meshheading:17057735-Receptor, Epidermal Growth Factor, pubmed-meshheading:17057735-Receptor, erbB-2, pubmed-meshheading:17057735-Recombinant Proteins, pubmed-meshheading:17057735-Stem Cells, pubmed-meshheading:17057735-Transforming Growth Factor alpha
pubmed:year
2007
pubmed:articleTitle
Transforming growth factor alpha promotes sequential conversion of mature astrocytes into neural progenitors and stem cells.
pubmed:affiliation
Inserm U114 and U752, Paris, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't