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Gopfert, M. C.

Publications and source records attributed to Gopfert, M. C..

2 recordsLinked to original sources

Mechanically-evoked spike responses of pentascolopidial chordotonal organs of Drosophila larvae

Stretch-sensitive ensembles of neurons in insects, known as Chordotonal organs (COs), function in proprioception, the detection of sound and substrate vibrations. Here we characterize the mechanical sensitivity of the lateral pentascolopidial CO (lch5) of Drosophila larvae to establish its postulated role in proprioception. We developed a physiologically realistic method to replicate proprioceptive input to lch5 by pulling the apodeme (tendon) to which the tips of the neurons attach. We found that lch5 sensory neurons respond transiently with a short latency to the velocity-component of stretch displacements and the release of stretch (relaxation). The mechanosensory mutant inactive, has a decreased response to mechanical stimuli and a lower overall spontaneous spike rate. Finally, we simulated the input that lch5 receives during crawling and observed spikes coincident with the start, middle and end of each peristaltic body contraction. We provide the first characterization of proprioceptive feedback in Drosophila larvae and firmly establish the proprioceptive function of lch5 in larval locomotion. Summary statementWe have characterized the spiking responses of the pentascolopidial chordotonal organ of 20 Drosophila larvae to mechanical stimuli and reveal a clear role in proprioception.

neuroscience↗

IFT88 transports Gucy2d, a guanylyl cyclase, to maintain sensory cilia function in Drosophila

Cilia are involved in a plethora of motility and sensory-related functions. Ciliary defects cause several ciliopathies, some of which with late-onset, suggesting cilia are actively maintained. While much is known about cilia assembly, little is understood about the mechanisms of their maintenance. Given that intraflagellar transport (IFT) is essential for cilium assembly, we investigated the role of one of its main players, IFT88, in ciliary maintenance. We show that DmIFT88, the Drosophila melanogaster orthologue of IFT88, continues to move along fully formed sensory cilia, and that its acute knockdown in the ciliated neurons of the adult affects sensory behaviour. We further identify DmGucy2d, the Drosophila guanylyl cyclase 2d, as a DmIFT88 cargo, whose loss also leads to defects in sensory behaviour maintenance. DmIFT88 binds to the intracellular part of DmGucy2d, which is evolutionarily conserved and mutated in several degenerative retina diseases, taking the cyclase into the cilia. Our results offer a novel mechanism for the maintenance of sensory cilia function and its potential role in human diseases.

cell biology↗