Synaptic depression induced by postsynaptic cAMP production in the Drosophila mushroom body calyx

Key points

Synaptic potentiation in Drosophila is observed at cholinergic synapses between antennal lobe (AL) and mushroom body (MB) neurons in the adult brain; however, depression at the AL–MB synapses has not yet been identified. By ex vivo Ca²⁺ imaging in an isolated cultured Drosophila brain, we found novel activity‐dependent depression at the AL–MB synapses. The degree of Ca²⁺ responses after repetitive AL stimulation is significantly reduced in the dendritic region of MB neurons (calyx) compared with those before AL stimulation, and this reduction of Ca²⁺ responses remains for at least 30 min. The expression of rutabaga, which encodes Ca²⁺/calmodulin‐dependent adenylyl cyclase, is essential in the MB neurons for the reduction of Ca²⁺ responses in the calyx. Our study reveals that elevation of cAMP production in the calyx during repetitive AL stimulation induces the depression at the AL–MB synapses.

Abstract

Synaptic plasticity has been studied to reveal the molecular and cellular mechanisms of associative and non‐associative learning. The fruit fly Drosophila melanogaster can be used to identify the molecular mechanisms of synaptic plasticity because vast genetic information or tools are available. Here, by ex vivo Ca²⁺ imaging of an isolated cultured Drosophila brain, we examined the novel activity‐dependent synaptic depression between the projection neurons of the antennal lobe (AL) and mushroom body (MB). Ex vivo Ca²⁺ imaging analysis revealed that electrical stimulation of AL elicits Ca²⁺ responses in the dendritic (calyx) and axonal (α lobe) regions of MB neurons, and the responses are reduced after repetitive AL stimulation. Since the cAMP signalling pathway plays an important role in synaptic plasticity in invertebrates and vertebrates, we examined whether the reduction of Ca²⁺ responses is also regulated by the cAMP signalling pathway. The expression of rutabaga (rut), which encodes Ca²⁺/calmodulin‐dependent adenylyl cyclase, was essential for the reduction of Ca²⁺ responses in the calyx and α lobe. Furthermore, imaging analysis using a fluorescence resonance energy transfer‐based cAMP indicator revealed that the cAMP level increased in the wild‐type calyx during repetitive AL stimulation, whereas it decreased in rut¹mutant flies with a loss‐of‐function mutation of rut. Thus, our study suggests that an increase in postsynaptic cAMP level during repetitive AL stimulation contributes to the attenuation of inputs at AL–MB synapses.

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