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J Neurosci 1999 Aug 15;1916:7066-76.
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Nitric oxide in the retinotectal system: a signal but not a retrograde messenger during map refinement and segregation.

Rentería RC , Constantine-Paton M .

The role of nitric oxide (NO) as a mediator of synaptic plasticity is controversial in both the adult and developing brain. NO generation appears to be necessary for some types of NMDA receptor-dependent synaptic plasticity during development but not for others. Our previous work using several NO donors revealed that Xenopus laevis retinal ganglion cell axons stop growing in response to NO exposure. We demonstrate here that the same response occurs in tectal neuron processes bathed in the NO donor S-nitrosocysteine (SNOC) and in RGC growth cones to which SNOC is very locally applied. We show that NO synthase (NOS) activity is present in the Rana pipiens optic tectum throughout development in a dispersed subpopulation of tectal neurons, although effects of NO on synaptic function in a Rana pipiens tectal slice were varied. We chronically inhibited NOS in doubly innervated Rana tadpole optic tecta using L-N(G)-nitroarginine methyl ester in Elvax. Despite significant NOS inhibition as measured biochemically, eye-specific stripes remained normally segregated. This suggests that NOS activity is not downstream of NMDA receptor activation during retinotectal synaptic competition because NMDA receptor activation is necessary for segregation of retinal afferents into ocular dominance stripes in the doubly innervated tadpole optic tectum. We conclude that NO has some signaling function in the retinotectal pathway, but this function is not critical to the mechanism that refines the projection and causes eye-specific stripes.

PubMed ID: 10436061
PMC ID: PMC6782861
Article link: J Neurosci
Grant support: [+]

Species referenced: Xenopus laevis
Genes referenced: mhc2-dab nos1 nos3 tecta.2
Antibodies: Nos1 Ab3

Article Images: [+] show captions
References [+] :
Ankri, Automatic detection of spontaneous synaptic responses in central neurons. 1994, Pubmed