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The Journal of Neuroscience, September 1, 1999, 19(17):7384-7393
Evidence of an Agrin Receptor in Cortical Neurons
Lutz G. W.
Hilgenberg,
Cameron L.
Hoover, and
Martin A.
Smith
Department of Anatomy and Neurobiology, University of California at
Irvine, Irvine, California 92697
Agrin plays a key role in directing the differentiation of the
vertebrate neuromuscular junction. Understanding agrin function at the
neuromuscular junction has come via molecular genetic analyses of agrin
as well as identification of its receptor and associated signal
transduction pathways. Agrin is also expressed by many populations of
neurons in brain, but its role remains unknown. Here we show, in
cultured cortical neurons, that agrin induces expression of the
immediate early gene c-fos in a
concentration-dependent and saturable manner, as expected for a signal
transduction pathway activated by a cell surface receptor. Agrin is
active in cortical neurons at picomolar concentrations, is
Ca2+ dependent, and is inhibited by heparin and
staurosporine. Despite marked differences in acetylcholine receptor
(AChR)-clustering activity, all alternatively spliced forms of agrin
are equally potent inducers of c-fos in cortical
neurons. A similar, isoform-independent response to agrin was also
observed in cultures prepared from the hippocampus and cerebellum. Only
agrin with high AChR-clustering activity was effective in cultured
muscle, whereas non-neuronal cells were agrin insensitive. Although
consistent with a receptor tyrosine kinase model similar to the
muscle-specific kinase-myotube-associated specificity component
complex in muscle, our data suggest that CNS neurons express a unique
agrin receptor. Evidence that neuronal signal transduction is mediated
via an increase in intracellular Ca2+ means that
agrin is well situated to influence important
Ca2+-dependent functions in brain, including
neuronal growth, differentiation, and adaptive changes in gene
expression associated with synaptic remodeling.
Key words:
agrin; signal transduction; c-fos; synapse
formation; neuromuscular junction; cortex
Copyright © 1999 Society for Neuroscience 0270-6474/99/19177384-10$05.00/0
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