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Calcium-stores mediate adaptation in axon terminals of Olfactory Receptor Neurons in Drosophila

BACKGROUND: In vertebrates and invertebrates, sensory neurons adapt to variable ambient conditions, such as the duration or repetition of a stimulus, a physiological mechanism considered as a simple form of non-associative learning and neuronal plasticity. Although various signaling pathways, as cAM...

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Detalles Bibliográficos
Autores principales: Murmu, Meena S, Stinnakre, Jacques, Réal, Eléonore, Martin, Jean-René
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226658/
https://www.ncbi.nlm.nih.gov/pubmed/22024464
http://dx.doi.org/10.1186/1471-2202-12-105
Descripción
Sumario:BACKGROUND: In vertebrates and invertebrates, sensory neurons adapt to variable ambient conditions, such as the duration or repetition of a stimulus, a physiological mechanism considered as a simple form of non-associative learning and neuronal plasticity. Although various signaling pathways, as cAMP, cGMP, and the inositol 1,4,5-triphosphate receptor (InsP(3)R) play a role in adaptation, their precise mechanisms of action at the cellular level remain incompletely understood. Recently, in Drosophila, we reported that odor-induced Ca(2+)-response in axon terminals of olfactory receptor neurons (ORNs) is related to odor duration. In particular, a relatively long odor stimulus (such as 5 s) triggers the induction of a second component involving intracellular Ca(2+)-stores. RESULTS: We used a recently developed in-vivo bioluminescence imaging approach to quantify the odor-induced Ca(2+)-activity in the axon terminals of ORNs. Using either a genetic approach to target specific RNAs, or a pharmacological approach, we show that the second component, relying on the intracellular Ca(2+)-stores, is responsible for the adaptation to repetitive stimuli. In the antennal lobes (a region analogous to the vertebrate olfactory bulb) ORNs make synaptic contacts with second-order neurons, the projection neurons (PNs). These synapses are modulated by GABA, through either GABAergic local interneurons (LNs) and/or some GABAergic PNs. Application of GABAergic receptor antagonists, both GABA(A )or GABA(B), abolishes the adaptation, while RNAi targeting the GABAB(R )(a metabotropic receptor) within the ORNs, blocks the Ca(2+)-store dependent component, and consequently disrupts the adaptation. These results indicate that GABA exerts a feedback control. Finally, at the behavioral level, using an olfactory test, genetically impairing the GABA(B)R or its signaling pathway specifically in the ORNs disrupts olfactory adapted behavior. CONCLUSION: Taken together, our results indicate that a relatively long lasting form of adaptation occurs within the axon terminals of the ORNs in the antennal lobes, which depends on intracellular Ca(2+)-stores, attributable to a positive feedback through the GABAergic synapses.