| Literature DB >> 16242215 |
Susanne Klumpp1, Dorothee Kriha, Gunther Bechmann, Alexander Maassen, Sandra Maier, Stefanie Pallast, Patrick Hoell, Josef Krieglstein.
Abstract
The aim of this work was to test whether growth factors such as basic fibroblast growth factor (bFGF), nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF) undergo autophosphorylation and whether this affects their biological activity. Incubation of those growth factors with [gamma-(32)P]ATP resulted in phosphorylation in vitro. The phosphate bond was resistant to alkaline pH, yet acid-labile. Addition of alkaline phosphatase resulted in time and protein dependent dephosphorylation. Concomitantly, alkaline phosphatase abolished the neuroprotective effect of those growth factors upon oxygen and glucose deprivation and upon staurosporine-induced cell death. For those studies, we were using primary cultures of cortical and hippocampal neurons from embryonic and neonatal rats. Incubation of bFGF with non-hydrolyzable ATP-gammaS resulted in phosphorylation and in neuroprotection resistant to alkaline phosphatase. We conclude that bFGF, NGF and BDNF undergo autophosphorylation on site(s) other than serine, threonine, tyrosine and/or ATP-binding, and that this binding of phosphate is essential for neuroprotection in vivo.Entities:
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Year: 2005 PMID: 16242215 DOI: 10.1016/j.neuint.2005.08.009
Source DB: PubMed Journal: Neurochem Int ISSN: 0197-0186 Impact factor: 3.921