Lorber, B.* ; Chew, D.J.* ; Hauck, S.M. ; Chong, R.S.* ; Fawcett, J.W.* ; Martin, K.R.*
Retinal glia promote dorsal root ganglion axon regeneration.
PLoS ONE 10:e0115996 (2015)
Axon regeneration in the adult central nervous system (CNS) is limited by several factors including a lack of neurotrophic support. Recent studies have shown that glia from the adult rat CNS, specifically retinal astrocytes and Müller glia, can promote regeneration of retinal ganglion cell axons. In the present study we investigated whether retinal glia also exert a growth promoting effect outside the visual system. We found that retinal glial conditioned medium significantly enhanced neurite growth and branching of adult rat dorsal root ganglion neurons (DRG) in culture. Furthermore, transplantation of retinal glia significantly enhanced regeneration of DRG axons past the dorsal root entry zone after root crush in adult rats. To identify the factors that mediate the growth promoting effects of retinal glia, mass spectrometric analysis of retinal glial conditioned medium was performed. Apolipoprotein E and secreted protein acidic and rich in cysteine (SPARC) were found to be present in high abundance, a finding further confirmed by western blotting. Inhibition of Apolipoprotein E and SPARC significantly reduced the neuritogenic effects of retinal glial conditioned medium on DRG in culture, suggesting that Apolipoprotein E and SPARC are the major mediators of this regenerative response.
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Publication type
Article: Journal article
Document type
Scientific Article
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Keywords
Receptor-related Protein-1; Apolipoprotein-e; Neurite Outgrowth; Mesangial Cells; Spinal-cord; In-vitro; Sparc; Survival; Lipoproteins; Osteonectin
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Language
english
Publication Year
2015
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2015
ISSN (print) / ISBN
1932-6203
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Volume: 10,
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Article Number: e0115996
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Public Library of Science (PLoS)
Publishing Place
Lawrence, Kan.
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Peer reviewed
POF-Topic(s)
30203 - Molecular Targets and Therapies
Research field(s)
Enabling and Novel Technologies
PSP Element(s)
G-505700-001
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Erfassungsdatum
2015-04-01