sensory experience differentially modulates the mrna expression of the polysialyltransferases st8siaii and st8siaiv in postnatal mouse visual cortex感官体验不同调节的mrna表达polysialyltransferases st8siaii和st8siaiv产后小鼠视觉皮质.pdfVIP
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sensory experience differentially modulates the mrna expression of the polysialyltransferases st8siaii and st8siaiv in postnatal mouse visual cortex感官体验不同调节的mrna表达polysialyltransferases st8siaii和st8siaiv产后小鼠视觉皮质
Sensory Experience Differentially Modulates the mRNA
Expression of the Polysialyltransferases ST8SiaII and
ST8SiaIV in Postnatal Mouse Visual Cortex
´
Marie-Claude Belanger, Graziella Di Cristo*
´ ´
CHU Sainte-Justine and Universite de Montreal, Montreal, Quebec, Canada
Abstract
Polysialic acid (PSA) is a unique carbohydrate composed of a linear homopolymer of a-2,8 linked sialic acid, and is mainly
attached to the fifth immunoglobulin-like domain of the neural cell adhesion molecule (NCAM) in vertebrate neural system.
In the brain, PSA is exclusively synthesized by the two polysialyltransferases ST8SiaII (also known as STX) and ST8SiaIV (also
known as PST). By modulating adhesive property of NCAM, PSA plays a critical role in several neural development processes
such as cell migration, neurite outgrowth, axon pathfinding, synaptogenesis and activity-dependent plasticity. The
expression of PSA is temporally and spatially regulated during neural development and a tight regulation of PSA expression
is essential to its biological function. In mouse visual cortex, PSA is downregulated following eye opening and its decrease
allows the maturation of GABAergic synapses and the opening of the critical period for ocular dominance plasticity.
Relatively little is known about how PSA levels are regulated by sensory experience and neuronal activity. Here, we
demonstrate that while both ST8SiaII and ST8SiaIV mRNA levels decrease around the time of eye opening in mouse visual
cortex, only ST8SiaII mRNA level reduction is regulated by sensory experience. Using an organotypic culture system from
mouse visual cortex, we further show that ST8SiaII gene expression is regulated by spiking activity and NMDA-mediated
excitation. Further, we show
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