WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience Join the Society for Neuroscience
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (36)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lander, C.
Right arrow Articles by Hockfield, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lander, C.
Right arrow Articles by Hockfield, S.

 Previous Article  |  Next Article 

The Journal of Neuroscience, January 1, 1998, 18(1):174-183

Neurons Produce a Neuronal Cell Surface-Associated Chondroitin Sulfate Proteoglycan

Cynthia Lander, Hong Zhang, and Susan Hockfield

Section of Neurobiology, Yale University School of Medicine, New Haven, Connecticut 06520-8001

Monoclonal antibody Cat-315 recognizes a chondroitin sulfate proteoglycan (CSPG) expressed on the surface of subsets of neurons in many areas of the mammalian CNS (). The cell type-specific expression exhibited by the Cat-315 CSPG and other perineuronal net CSPGs imparts a distinct molecular surface identity to a neuron (; ). The cell type(s) producing these surface-associated proteins and yielding this cellular diversity has remained in question. The expression of the Cat-315 CSPG in primary rat cortical cultures has permitted an examination of the cellular source of the Cat-315 antigen, as well as a determination of its spatial relationship to the neuronal surface.

Live-cell labeling of primary neuronal cultures demonstrates that the Cat-315 CSPG is on the extracellular surface of neurons. Furthermore, extraction experiments demonstrate that the Cat-315 CSPG lacks a transmembrane domain and that the entire molecule is extracellular and, therefore, can be considered a constituent of brain extracellular matrix. Several lines of evidence indicate that neurons with cell surface staining produce the Cat-315 CSPG. First, neurons with cell surface staining also show intracellular Cat-315 immunoreactivity. Second, beta -xyloside or monensin, reagents that inhibit the synthesis and transport of CSPGs, increase intracellular Cat-315 immunoreactivity within neurons that express cell surface Cat-315 immunoreactivity. Third, double labeling with Cat-315 and a polyclonal antibody for the Golgi complex demonstrates a precise colocalization of the intracellular Cat-315 immunoreactivity with the Golgi. Together, these observations demonstrate that neurons contribute to the extracellular matrix of brain and that the Cat-315 CSPG is produced by the neurons that carry Cat-315 cell surface immunoreactivity.

Key words: perineuronal net; brain extracellular matrix; neuronal subsets; rat cortex; primary neuronal cultures; glycosaminoglycan


Copyright © 1998 Society for Neuroscience  0270-6474/98/181174-10$05.00/0


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
K. L. Abbott, R. T. Matthews, and M. Pierce
Receptor Tyrosine Phosphatase {beta} (RPTP{beta}) Activity and Signaling Are Attenuated by Glycosylation and Subsequent Cell Surface Galectin-1 Binding
J. Biol. Chem., November 28, 2008; 283(48): 33026 - 33035.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. P. Steinmetz, K. P. Horn, V. J. Tom, J. H. Miller, S. A. Busch, D. Nair, D. J. Silver, and J. Silver
Chronic Enhancement of the Intrinsic Growth Capacity of Sensory Neurons Combined with the Degradation of Inhibitory Proteoglycans Allows Functional Regeneration of Sensory Axons through the Dorsal Root Entry Zone in the Mammalian Spinal Cord
J. Neurosci., August 31, 2005; 25(35): 8066 - 8076.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
R. T. Matthews, G. M. Kelly, C. A. Zerillo, G. Gray, M. Tiemeyer, and S. Hockfield
Aggrecan Glycoforms Contribute to the Molecular Heterogeneity of Perineuronal Nets
J. Neurosci., September 1, 2002; 22(17): 7536 - 7547.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
B. P. Niederost, D. R. Zimmermann, M. E. Schwab, and C. E. Bandtlow
Bovine CNS Myelin Contains Neurite Growth-Inhibitory Activity Associated with Chondroitin Sulfate Proteoglycans
J. Neurosci., October 15, 1999; 19(20): 8979 - 8989.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. A. Nastuk, S. Davis, G. D. Yancopoulos, and J. R. Fallon
Expression Cloning and Characterization of NSIST, a Novel Sulfotransferase Expressed by a Subset of Neurons and Postsynaptic Targets
J. Neurosci., September 15, 1998; 18(18): 7167 - 7177.
[Abstract] [Full Text] [PDF]



-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2009 by Society for Neuroscience ONLINE ISSN: 1529-2401
-