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Localization of chondroitin sulfate proteoglycan versican in adult brain with special reference to large projection neurons
Authors:Noriko Horii-Hayashi  Hiroaki Okuda  Kouko Tatsumi  Shigeaki Ishizaka  Masahide Yoshikawa  Akio Wanaka
Affiliation:(1) Department of Parasitology, Faculty of Medicine, Nara Medical University, Kashihara, Nara 634-8521, Japan;(2) 2nd Department of Anatomy, Faculty of Medicine, Nara Medical University, Kashihara, Nara 634-8521, Japan
Abstract:Versican is a chondroitin sulfate proteoglycan belonging to the lectican family. Versican has two glycosaminoglycan attachment regions, named the GAGα and GAGβ domains, which are both regulated by alternative splicing and yield four protein isoforms. We have investigated the expression and localization of versican in the developing and adult brain by using anti-versican GAGα and GAGβ antibodies. Western analysis revealed that GAGα-reactive isoform was dominant in the adult brain. Immunohistochemical study demonstrated that GAGα immunoreactivity was detectable from neonatal periods to adulthood, whereas GAGβ immunoreactivity completely disappeared within 3 weeks of birth. In the adult brain, GAGα immunoreactivity was seen in the white matter regions and was also localized in the gray matter including somata and dendrites of cortical and hippocampal pyramidal neurons and cerebellar Purkinje cells. In contrast, GAGα immunoreactivity was not localized on parvalbumin-positive interneurons and cerebellar stellate cells. Furthermore, GAGα immunoreactivity was not co-localized with perineuronal net markers such as Wisteria floribunda agglutinin lectin and phosphacan. Thus, versican was localized on large projection neurons rather than small interneurons. To confirm the binding mechanism of versican to neurons, hyaluronan and chondroitin sulfates were enzymatically removed from brain sections before the immunolabeling of versican. These treatments had no effect on the labeling pattern of versican, suggesting that other versican-interactive molecules are involved in the binding of versican to neurons. This study was supported by a Grant-in-Aid for Scientific Research on Priority Areas “Advanced Brain Science Project” from the Ministry of Education, Culture, Sports, Science, and Technology, Japan.
Keywords:Chondroitin sulfate proteoglycans  Extracellular matrix  Neurons  Immunohistochemistry  Brain  Versican  Mouse (C57BL/6J)
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