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The Journal of Neuroscience, September 1, 2002, 22(17):7536-7547
Aggrecan Glycoforms Contribute to the Molecular Heterogeneity of
Perineuronal Nets
Russell T.
Matthews1,
Gail M.
Kelly1,
Cynthia A.
Zerillo1,
Grace
Gray1,
Michael
Tiemeyer2, and
Susan
Hockfield1
1 Department of Neurobiology, Yale University School of
Medicine, New Haven, Connecticut 06520, and 2 Glyko, Inc.,
Novato, California, 94949
The perineuronal net forms the extracellular matrix of many neurons
in the CNS, surrounding neuron cell bodies and proximal dendrites in a
mesh-like structure with open "holes" at the sites of synaptic
contacts. The perineuronal net is first detected late in development,
approximately coincident with the transformation of the CNS from an
environment conducive to neuronal growth and motility to one that is
restrictive, suggesting a role for the perineuronal net in this
developmental transition. Perineuronal nets show a great degree of
molecular heterogeneity. Using monoclonal antibodies Cat-301, Cat-315,
and Cat-316, we have shown previously that although all antibodies
recognize chondroitin sulfate proteoglycans of similar sizes, each
antibody recognizes perineuronal nets on distinct but overlapping sets
of neurons in the adult cat CNS. An understanding of the heterogeneity
demonstrated by these antibodies is critical to understanding the
organization and function of perineuronal nets. Using aggrecan
knock-out mice (cmd), we have now determined that all
three antibodies recognize aggrecan. Chemical and enzymatic
deglycosylation show that the differences revealed by the three
antibodies arise from differential glycosylation of aggrecan. We
further demonstrate that aggrecan mRNA is expressed relatively late in development and that neurons themselves are likely
the predominant cellular sites of aggrecan expression. This work indicates that neurons can directly regulate the composition of their extracellular matrix by regulated synthesis and differential glycosylation of aggrecan in a cell type-specific manner. These results
have important implications for the role of regulated microheterogeneity of glycosylation in the CNS.
Key words:
chondroitin sulfates; proteoglycans; glycosylation; lectican; extracellular matrix; synapse formation
Copyright © 2002 Society for Neuroscience 0270-6474/02/22177536-12$05.00/0
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