Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0110668
Title: BMP Signaling in astrocytes downregulates EGFR to modulate survival and maturation
Authors: Scholze A.R.
Foo L.C. 
Mulinyawe S.
Barres B.A.
Keywords: aquaporin 4
bone morphogenetic protein
bone morphogenetic protein 5
epidermal growth factor receptor
fibroblast growth factor
glial fibrillary acidic protein
protein S100B
Smad1 protein
Smad5 protein
Smad8 protein
somatomedin B
Wnt7a protein
bone morphogenetic protein
Egfr protein, rat
epidermal growth factor receptor
animal cell
animal tissue
Article
astrocyte
cell differentiation
cell heterogeneity
cell lineage
cell maturation
cell proliferation
cell survival
controlled study
down regulation
immunoblotting
immunoreactivity
in vitro study
nonhuman
oligodendroglia
prospective study
protein analysis
protein expression
protein phosphorylation
purification
rat
signal transduction
upregulation
animal
astrocyte
biosynthesis
gene expression regulation
genetics
metabolism
mouse
phosphorylation
physiology
signal transduction
Animals
Astrocytes
Bone Morphogenetic Proteins
Gene Expression Regulation, Developmental
Mice
Phosphorylation
Rats
Receptor, Epidermal Growth Factor
Signal Transduction
Issue Date: 2014
Citation: Scholze A.R., Foo L.C., Mulinyawe S., Barres B.A. (2014). BMP Signaling in astrocytes downregulates EGFR to modulate survival and maturation. PLoS ONE 9 (10) : e110668. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0110668
Rights: Attribution 4.0 International
Abstract: Astrocytes constitute a major cell population in the brain with a myriad of essential functions, yet we know remarkably little about the signaling pathways and mechanisms that direct astrocyte maturation. To explore the signals regulating astrocyte development, we prospectively purified and cultured immature postnatal rodent astrocytes. We identified fibroblast growth factors (FGFs) and bone morphogenetic proteins (BMPs) as robust trophic factors for immature astrocytes. We showed that astrocytes respond directly to BMPs via phosphorylation of the smad1/5/8 pathway. In vitro, BMP signaling promoted immature astrocytes to adopt multiple characteristics of mature astrocytes, including a more process-bearing morphology, aquaporin-4 (AQP4) and S100? immunoreactivity, limited proliferation, and strong downregulation of epidermal growth factor receptor (EGFR). In vivo, activation of the smad1/5/8 pathway in astrocytes was seen during early postnatal development, but inhibition of astrocyte proliferation was not observed. These insights can aid in the further dissection of the mechanisms and pathways controlling astrocyte biology and development. © 2014 Scholze et al.
Source Title: PLoS ONE
URI: https://scholarbank.nus.edu.sg/handle/10635/161767
ISSN: 19326203
DOI: 10.1371/journal.pone.0110668
Rights: Attribution 4.0 International
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