The myelin-associated glycoprotein inhibitor BENZ induces outgrowth and survival of rat dorsal root ganglion cell cultures
✍ Scribed by Marcin Nowicki; Joanna Kosacka; Reinhard Brossmer; Katharina Spanel-Borowski; Jürgen Borlak
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 623 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0360-4012
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✦ Synopsis
Abstract
The novel myelin‐associated glycoprotein (MAG) inhibitor BENZ binds to the N‐acetylneuraminic acid (Neu5Ac) portion of the N‐terminal Ig‐like domain of MAG. Treatment of rat dorsal root ganglion (DRG) cell cultures with BENZ‐induced outgrowth of neurofilament 200–positive neurites improved survival of neurons and increased the number of GFAP‐positive cells, as determined by fluorescence and confocal laser microscopy and by Western immunoblotting. Furthermore, treatment of DRG cell cultures with BENZ repressed gene and protein expression of the small GTPase RhoA but induced expression of Rho GTP–activating proteins 5 and 24, likely to counteract protein kinase A activity. Specifically, expression of inhibitors of neurite outgrowth, for example, Rock2 and PAK4, was repressed, but cofilin 1, a promoter of axonal growth, was induced. We propose that the MAG inhibitor BENZ abrogates the RhoA–ROCK–cofilin pathway to promote neurite outgrowth. Our findings require confirmation by in vivo animal studies. © 2007 Wiley‐Liss, Inc.