Absence of GAP-43 can protect neurons from death

The main function of GAP-43 is thought to be regulating growth cone motilit y and axon guidance signals. GAP-43 is highly expressed during development and in regenerating nerves and in particular regions of the adult brain. We here present the first evidence that GAP-43 can modulate guidance signals emanating from Semaphorin III (SemaIII) in cultured NGF-dependent sensory n eurons. We further show that absence of GAP-43 dramatically increases resis tance of specific sensory neurons to apoptotic stimuli in vitro. NGF-depend ent sensory neurons from GAP-43 (+/-) and null mutant mice are strongly pro tected against SemaIII-induced death. Furthermore, NGF- and BDNF-dependent neurons, but not NT-3-dependent neurons, from GAP-43 null mutant mice are m uch more resistant to apoptosis induced by trophic factor deprivation. We a lso show that early postnatal Purkinje cells from GAP-43 (+/-) mice are mor e resistant to cell death in organotypic cultures. We conclude that GAP-43 can influence neuronal survival and modulate repulsive axon guidance signal s.