Cerebroglycan, a developmentally regulated cell-surface heparan sulfate proteoglycan, is expressed on developing axons and growth cones

Jonathan K. Ivins*, E. David Litwack, Asli Kumbasar, Christopher S. Stipp, Arthur D. Lander

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

66 Citations (Scopus)

Abstract

Cerebroglycan is a glycosylphosphatidylinositol-linked integral membrane heparan sulfate proteoglycan found exclusively in the developing nervous system. In the rodent, cerebroglycan mRNA first appears in regions containing newly generated neurons and typically disappears 1 to several days later (Stipp et al., 1994, J. Cell Biol. 124:149-160). To gain insight into the roles that cerebroglycan plays in the developing nervous system, monospecific antibodies were prepared and used to localize cerebroglycan protein. In the rat, cerebroglycan was prominently expressed on axon tracts throughout the developing brain and spinal cord, where it was found at times when axons are actively growing, but generally not after axons have reached their targets. Cerebroglycan was also found on neuronal growth cones both in vivo and in vitro. Interestingly, cerebroglycan immunoreactivity was rarely seen in or around neuronal cell bodies. Indeed, by examining the hippocampus at a late stage in development-when most neurons no longer express cerebroglycan but newly generated granule neurons do-evidence was obtained that cerebroglycan is strongly polarized to the axonal, and excluded from the somatodendritic, compartment of neurons. The timing and pattern of cerebroglycan expression are consistent with a role for this cell-surface heparan sulfate proteoglycan in regulating the growth or guidance of axons.

Original languageEnglish
Pages (from-to)320-332
Number of pages13
JournalDevelopmental Biology
Volume184
Issue number2
DOIs
Publication statusPublished - 15 Apr 1997
Externally publishedYes

Funding

We are grateful to Merton Bern®eld for the gift of antiserum to syndecan-3. We thank Tim Fritz and Cathy Krull for helpful comments on the manuscript. This work was supported by NIH Grant NS26862 to A.D.L.

FundersFunder number
National Institutes of Health
National Institute of Neurological Disorders and StrokeR01NS026862

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