Glycobiology Advance Access published online on May 14, 2008
Glycobiology, doi:10.1093/glycob/cwn040
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Spatiotemporal expression of chondroitin sulfate sulfotransferases in the postnatal developing mouse cerebellum
Department of Developmental Neuroscience, Tokyo Metropolitan Institute for Neuroscience, Musashidai, Fuchu, Tokyo 183-8526, Japan
1 To whom correspondence should be addressed: Tel: 81-42-325-3881; Fax: 81-42-321-8678; e-mail: maedan{at}tmin.ac.jp
Received on April 3, 2008; accepted on May 10, 2008
Chondroitin sulfate (CS) proteoglycans are major components of the cell surface and the extracellular matrix in the developing brain, and bind to various proteins via CS chains in a CS structure-dependent manner. This study demonstrated the expression pattern of three CS sulfotransferase genes, dermatan 4-O-sulfotransferase (D4ST), uronyl 2-O-sulfotransferase (UST), and N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase (GalNAc4S-6ST), in the mouse postnatal cerebellum. These sulfotransferases are responsible for the biosynthesis of oversulfated structures in CS chains such as B-, D-, and E-units, which constitute the binding sites for various heparin-binding proteins. Real-time reverse transcription-polymerase chain reaction analysis indicated that the expression of UST increased remarkably during cerebellar development. The amounts of B and D units, which are generated by UST activity, in the cerebellar CS chains also increased during development. On the contrary, the expression of GalNAc4S-6ST and its biosynthetic product, E unit, decreased during postnatal development. In situ hybridization experiments revealed the levels of UST and GalNAc4S-6ST mRNAs to correlate inversely in many cells including Purkinje cells, granule cells in the external granular layer, and inhibitory interneurons. In these neurons, the expression of UST increased and that of GalNAc4S-6ST decreased during development and/or maturation. D4ST was also expressed by many neurons, but its expression was not simply correlated with development, which might contribute to the diversification of CS structures expressed by distinct neurons. These results suggest that the CS structures of various cerebellar neurons change during development and such changes of CS are involved in the regulation of various signaling pathways.
Key words: cerebellum / chondroitin sulfate / dermatan 4-O-sulfotransferase / N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase / uronyl 2-O-sulfotransferase
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