Manipulation of Neural Circuits in Drosophila Larvae

Author(s):  
Ibrahim Tastekin ◽  
Matthieu Louis
2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Atsuki Hiramoto ◽  
Julius Jonaitis ◽  
Sawako Niki ◽  
Hiroshi Kohsaka ◽  
Richard D. Fetter ◽  
...  

AbstractTypical patterned movements in animals are achieved through combinations of contraction and delayed relaxation of groups of muscles. However, how intersegmentally coordinated patterns of muscular relaxation are regulated by the neural circuits remains poorly understood. Here, we identify Canon, a class of higher-order premotor interneurons, that regulates muscular relaxation during backward locomotion of Drosophila larvae. Canon neurons are cholinergic interneurons present in each abdominal neuromere and show wave-like activity during fictive backward locomotion. Optogenetic activation of Canon neurons induces relaxation of body wall muscles, whereas inhibition of these neurons disrupts timely muscle relaxation. Canon neurons provide excitatory outputs to inhibitory premotor interneurons. Canon neurons also connect with each other to form an intersegmental circuit and regulate their own wave-like activities. Thus, our results demonstrate how coordinated muscle relaxation can be realized by an intersegmental circuit that regulates its own patterned activity and sequentially terminates motor activities along the anterior-posterior axis.


SLEEP ◽  
2020 ◽  
Vol 43 (Supplement_1) ◽  
pp. A9-A9
Author(s):  
A R Poe ◽  
M Szuperak ◽  
M S Kayser

Abstract Introduction Sleep during early life is thought to be important for brain development. Indeed, disruptions in sleep during development have long-lasting effects on cognitive functioning. Recently, our lab has developed the LarvaLodge platform for monitoring sleep in developing Drosophila larvae. Using this system we can investigate the neural circuits and signals controlling sleep during early neurodevelopmental periods. Neuropeptides play critical roles in regulating many behaviors in both larvae and adult flies.While several neuropeptides modulate sleep in adult flies, it is not known what role neuropeptides play in controlling larval sleep. Methods To identify peptidergic neurons that regulate 2nd instar larval sleep, we activated neurons labeled by 34 independent Gal4 driver lines corresponding to 25 different neuropeptide genes using the heat-sensitive cation channel, TrpA1. Results Of the 34 Gal4 driver lines, we determined that 2 lines are wake-promoting and 7 lines are sleep-promoting. A subset of these exert effects on sleep without associated changes in wake activity levels. We also observed sleep fragmentation (increase in sleep bout number and decrease in sleep bout length) in 3 lines. Subsequent analysis indicated that manipulation of activity in Diuretic hormone 44 (Dh44)-labeled neurons bidirectionally modulates sleep-wake. Additionally, pan-neuronal knockdown of Dh44 altered sleep duration. Conclusion This work indicates that neuropeptidergic signaling modulates sleep during early development and provides a platform to examine how neuropeptidergic regulation of sleep/wake changes throughout the lifespan. Support NIH T32


2009 ◽  
Vol 101 (6) ◽  
pp. 3075-3088 ◽  
Author(s):  
Stefan R. Pulver ◽  
Stanislav L. Pashkovski ◽  
Nicholas J. Hornstein ◽  
Paul A. Garrity ◽  
Leslie C. Griffith

In recent years, a number of tools have become available for remotely activating neural circuits in Drosophila. Despite widespread and growing use, very little work has been done to characterize exactly how these tools affect activity in identified fly neurons. Using the GAL4-UAS system, we expressed blue light–gated Channelrhodopsin-2 (ChR2) and a mutated form of ChR2 (H134R-ChR2) in motor and sensory neurons of the Drosophila third-instar locomotor circuit. Neurons expressing H134R-ChR2 show enhanced responses to blue light pulses and less spike frequency adaptation than neurons expressing ChR2. Although H134R-ChR2 was more effective at manipulating behavior than ChR2, the behavioral consequences of firing rate adaptation were different in sensory and motor neurons. For comparison, we examined the effects of ectopic expression of the warmth-activated cation channel Drosophila TRPA1 (dTRPA1). When dTRPA1 was expressed in larval motor neurons, heat ramps from 21 to 27°C evoked tonic spiking at ∼25°C that showed little adaptation over many minutes. dTRPA1 activation had stronger and longer-lasting effects on behavior than ChR2 variants. These results suggest that dTRPA1 may be particularly useful for researchers interested in activating fly neural circuits over long time scales. Overall, this work suggests that understanding the cellular effects of these genetic tools and their temporal dynamics is important for the design and interpretation of behavioral experiments.


2012 ◽  
Vol 7 (8) ◽  
pp. 1470-1478 ◽  
Author(s):  
Ken Honjo ◽  
Richard Y Hwang ◽  
William Daniel Tracey

2001 ◽  
Vol 120 (5) ◽  
pp. A177-A177
Author(s):  
S SHARP ◽  
J YU ◽  
J GUZMAN ◽  
J XUE ◽  
H COOKE ◽  
...  

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