Divergent regulation of GAP-43 expression and CNS neurite outgrowth by cyclic AMP

✍ Scribed by Parker L. Andersen; Christine A. Webber; Scott R. Whittemore; David J. Schreyer

• Publisher: John Wiley and Sons
• Year: 2000
• Tongue: English
• Weight: 368 KB
• Volume: 61
• Category: Article
• ISSN: 0360-4012
• DOI: 10.1002/1097-4547(20000915)61:6<626::aid-jnr6>3.0.co;2-j

✦ Synopsis

Robust process outgrowth and high expression of the growth-associated protein GAP-43 seem to be intrinsic features of neurons, but both are down-regulated after axonal contact of target cells. We report that chronic exposure of the serotonergic CNS cell line RN46A to cyclic AMP analogs, forskolin, or cholera toxin represses GAP-43 expression in a dose dependent manner. Thus, cAMP could mediate a GAP-43 repressive signal that is initiated extracellularly. Activation of the cyclic AMP pathway by these same reagents, however, enhances the rate that RN46A cells extend neurites. This stimulation of neurite growth can occur during inhibition of new transcription, and in the absence of high levels of GAP-43. These findings demonstrate that a GAP-43-repressing intracellular signaling pathway exists, that repression of GAP-43 expression by cAMP is not directly coupled to inhibition of neurite growth, and that acceleration of growth cone advancement by cAMP is not dependent on the presence of GAP-43.