Abstract
Glypican-1, a heparan sulfate proteoglycan, is expressed in various tissues including developing and postnatal central nervous system. It serves as a receptor for heparin-binding molecules such as fibroblast growth factors (FGFs). We investigated whether glypican-1 was expressed after brain injury in adult mice. In situ hybridization study showed that glypican-1 mRNA was expressed in the region surrounding necrotic tissue, and that the signal intensity peaked 7 days after the cryo-injury. In addition, both FGF-2 and amyloid precursor protein (APP) were concurrently upregulated and colocalized with glypican-1 mRNA. Since FGF-2 and APP can bind to glypican-1 in vitro, the present study suggested that their autocrine/paracrine interactions with glypican-1 may be involved in neuronal regeneration and/or neurite-outgrowth inhibition after brain injury.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amyloid beta-Protein Precursor / metabolism
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Animals
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Astrocytes / metabolism
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Autocrine Communication / genetics
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Brain / metabolism*
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Brain / physiopathology
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Brain Injuries / genetics
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Brain Injuries / metabolism*
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Brain Injuries / physiopathology
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Disease Models, Animal
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Fibroblast Growth Factor 2 / metabolism
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Gene Expression / physiology
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Gliosis / metabolism
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Gliosis / physiopathology
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Growth Cones / metabolism
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Growth Cones / ultrastructure
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Growth Substances / metabolism*
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Heparan Sulfate Proteoglycans / genetics*
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Male
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Mice
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Mice, Inbred ICR
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Nerve Regeneration / genetics*
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Neurites / metabolism
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Neurites / ultrastructure
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RNA, Messenger / metabolism
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Recovery of Function / genetics*
Substances
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Amyloid beta-Protein Precursor
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Growth Substances
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Heparan Sulfate Proteoglycans
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RNA, Messenger
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Fibroblast Growth Factor 2