Search bioRxiv⌕ Search

Biology subjects

MacLeod, J.

Publications and source records attributed to MacLeod, J..

2 recordsLinked to original sources

Dopamine promotes motor programs underlying substrate tunneling in larval Drosophila

Dopamine is a conserved biogenic amine with diverse neuromodulatory roles. Here we examine the role of dopamine in modulating larval Drosophila melanogaster motor programs underlying movement over and through substrates. First, we performed dual-color calcium imaging in tyrosine hydroxylase (TH)-expressing dopaminergic neurons and motor neurons to reveal cell-type specific recruitment patterns during fictive motor programs. Activity of select TH-neurons correlated strongly with fictive headsweeps as well as forward and backward locomotion. Next, bath applications of dopamine biased the isolated central nervous system towards fictive forward locomotion and inhibited fictive headsweeps. To probe whether these effects are recapitulated in intact animals, we optogenetically manipulated TH-neuron activity during surface crawling and tunneling. Optogenetic activation of TH-neurons with CsChrimson during crawling had no effect on headsweeps and slowed locomotor rhythms by increasing wave duration and decreasing wave frequency. Furthermore, posterior asymmetries, motor sequences characteristic of tunneling, were triggered. On the other hand, optogenetically inhibiting TH-neurons with GtACR1 had little effect on surface crawling. Underground, TH-neuron activation enhanced tunneling activity by increasing wave frequency, instead of duration, which increased overall time spent tunnelling, whereas inhibition decreased time spent tunneling. These results suggest that dopaminergic modulation of larval forward locomotion is dependent on sensorimotor context. We propose dopamine mediates a coordinated network effort to shift central pattern generators to promote tunneling-specific motor programs. New & NoteworthyHere, we find Drosophila larval dopaminergic neurons exhibit cell-type-specific activity in relation to fictive motor patterns. Furthermore, pharmacological and optogenetic manipulations of dopaminergic signaling acutely modifies locomotor output. Specifically, dopamine application promotes forward locomotion and inhibits headsweeps in isolated preparations, while optogenetically activating TH-neurons in freely behaving larvae mediates a shift from crawling to tunneling motor programs. This provides new insights into context-dependent dopaminergic modulation of locomotion in a genetically tractable invertebrate.

neuroscience↗

Localization of muscarinic acetylcholine receptor dependent rhythm generating modules in the Drosophila larval locomotor network

Mechanisms of rhythm generation have been extensively studied in motor systems that control locomotion over terrain in limbed animals; however, much less is known about rhythm generation in soft-bodied terrestrial animals. Here we explored how muscarinic acetylcholine receptor (mAChR) dependent rhythm generating networks are distributed in the central nervous system (CNS) of soft-bodied Drosophila larvae. We measured fictive motor patterns in isolated CNS preparations using a combination of Ca2+ imaging and electrophysiology while manipulating mAChR signalling pharmacologically. Bath application of the mAChR agonist oxotremorine potentiated rhythm generation in distal regions of the isolated CNS, whereas application of the mAChR antagonist scopolamine suppressed rhythm generation in these regions. Oxotremorine raised baseline Ca2+ levels and potentiated rhythmic activity in isolated posterior abdominal CNS segments as well as isolated anterior brain and thoracic regions, but did not induce rhythmic activity in isolated anterior abdominal segments. Bath application of scopolamine to reduced preparations lowered baseline Ca2+ levels and abolished rhythmic activity. These results suggest the presence of a bimodal gradient of rhythmogenicity in the larval CNS, with mAChR dependent rhythm generating networks in distal regions separated by medial segments with severely reduced rhythmogenic abilities. This work furthers our understanding of motor control in soft-bodied locomotion and provides a foundation for study of rhythm generating networks in an emerging genetically tractable locomotor system.

neuroscience↗