IOVS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
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 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 Google Scholar
Google Scholar
Right arrow Articles by Inatani, M.
Right arrow Articles by Honda, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Inatani, M.
Right arrow Articles by Honda, Y.
(Investigative Ophthalmology and Visual Science. 2000;41:4338-4346.)
© 2000 by The Association for Research in Vision and Ophthalmology, Inc.

Neuroglycan C, a Neural Tissue–Specific Transmembrane Chondroitin Sulfate Proteoglycan, in Retinal Neural Network Formation

Masaru Inatani1, Hidenobu Tanihara2, Atsuhiko Oohira3, Yasumasa Otori4, Akihiro Nishida1, Megumi Honjo1, Noriaki Kido1 and Yoshihito Honda1

1 From the Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine; the 2 Department of Ophthalmology, Tenri Hospital; the 3 Department of Perinatology, Institute for Developmental Research, Aichi Human Service Center; and the 4 Department of Ophthalmology and Visual Science, Osaka University, Japan.

PURPOSE. Neuroglycan C (NGC) is a transmembrane chondroitin sulfate proteoglycan present exclusively in central nervous system tissues. In the current study the expression pattern and characterization of NGC during the development of the retina were investigated.

METHODS. Expressional changes of NGC mRNAs during rat retinal development were examined by semiquantitative reverse transcription–polymerase chain reaction (RT-PCR). The localization and characterization of NGC core proteins were investigated by immunoblot analysis and immunohistochemistry using an anti-NGC antibody.

RESULTS. Immunohistochemical analysis revealed that NGC was highly expressed in the nerve fiber layer (NFL) and inner plexiform layer (IPL) in rat postnatal developing retina. At embryonal stages, NGC immunoreactivities were faint. In contrast, at postnatal developmental stages (approximately postnatal day [P]7), intense immunoreactivity was observed in the NFL and IPL, where active dendrite branching was observed, and conventional synapses began to be formed. As retinal layer differentiation proceeded (from P14 to P42), immunoreactivities in the inner retinal layers gradually became fainter. Immunoblot and semiquantitative RT-PCR analyses showed that the peak level of NGC expression occurred on approximately P7 and P14. Glycosylation of the NGC core protein changed as the retinal layers matured. In immunoelectron microscopic analysis, NGC immunoreactivity was located on the axonal membranes of neuronal cells in the postnatal retina, whereas immunoreactivity was reduced on membranes at the adult stage. In retinal ganglion cells in vitro, NGC was highly localized in their spiny budding neurites.

CONCLUSIONS. The results show spatiotemporal expression patterns of NGC, and suggest that it plays a role in the formation of neural networks in retinal development.




This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
K. Nakanishi, S. Aono, K. Hirano, Y. Kuroda, M. Ida, Y. Tokita, F. Matsui, and A. Oohira
Identification of Neurite Outgrowth-promoting Domains of Neuroglycan C, a Brain-specific Chondroitin Sulfate Proteoglycan, and Involvement of Phosphatidylinositol 3-Kinase and Protein Kinase C Signaling Pathways in Neuritogenesis
J. Biol. Chem., August 25, 2006; 281(34): 24970 - 24978.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
Y. Inoue, M. Yoneda, J. Zhao, O. Miyaishi, A. Ohno-Jinno, T. Kataoka, Z. Isogai, K. Kimata, M. Iwaki, and M. Zako
Molecular Cloning and Characterization of Chick SPACRCAN
J. Biol. Chem., April 14, 2006; 281(15): 10381 - 10388.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. Aono, Y. Tokita, T. Shuo, S. Yamauchi, F. Matsui, K. Nakanishi, K. Hirano, M. Sano, and A. Oohira
Glycosylation Site for Chondroitin Sulfate on the Neural Part-time Proteoglycan, Neuroglycan C
J. Biol. Chem., November 5, 2004; 279(45): 46536 - 46541.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. ProteomicsHome page
V. L. Bonilha, S. K. Bhattacharya, K. A. West, J. Sun, J. W. Crabb, M. E. Rayborn, and J. G. Hollyfield
Proteomic Characterization of Isolated Retinal Pigment Epithelium Microvilli
Mol. Cell. Proteomics, November 1, 2004; 3(11): 1119 - 1127.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
B. Hassel, M. Schreff, E.-M. Stube, U. Blaich, and S. Schumacher
CALEB/NGC Interacts with the Golgi-associated Protein PIST
J. Biol. Chem., October 10, 2003; 278(41): 40136 - 40143.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
Y. Zhang, U. Rauch, and M.-T. R. Perez
Accumulation of Neurocan, a Brain Chondroitin Sulfate Proteoglycan, in Association with the Retinal Vasculature in RCS Rats
Invest. Ophthalmol. Vis. Sci., March 1, 2003; 44(3): 1252 - 1261.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
M. Inatani, M. Honjo, A. Oohira, N. Kido, Y. Otori, Y. Tano, Y. Honda, and H. Tanihara
Spatiotemporal Expression Patterns of N-Syndecan, a Transmembrane Heparan Sulfate Proteoglycan, in Developing Retina
Invest. Ophthalmol. Vis. Sci., May 1, 2002; 43(5): 1616 - 1621.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2000 by the Association for Research in Vision and Ophthalmology