The sensation of mechanical signals is vital for all animals. For this task Drosophila larvae are equipped with chordotonal organs. These are specialized mechanosensory organs which are composed of multicellular subunits. In this study I show how metabotropic signaling by the adhesion GCPR CIRL interacts with part of the ionotropic pathways during mechanosensation in sensory neurons of the pentascolopidial chordotonal organ (lch5). CIRL modulates cAMP levels in sensory neurons and thereby shapes the receptor potential response to mechanical stimuli. Here, CIRL forms a functional interaction with the TRP channel NOMPC in which nompC is epistatic to Cirl. Furthermore, the evidence presented suggest the presence of another target of CIRL and the involvement of a further signaling pathway besides cAMP modulation. In the second part of the study, I describe a method to express the anion-selective channelrhodopsin GtACR1 in individual of the five neurons of the lch5. For this I used the MARCM approach which
generates genetic mosaics during the development of the neurons of interest. Thereby a specific subset of cells deriving from a common precursor expresses the desired protein GtACR1.
| Identifer | oai:union.ndltd.org:DRESDEN/oai:qucosa:de:qucosa:79756 |
| Date | 27 June 2022 |
| Creators | Dahlhoff, Stefan |
| Contributors | Universität Leipzig |
| Source Sets | Hochschulschriftenserver (HSSS) der SLUB Dresden |
| Language | English |
| Detected Language | English |
| Type | info:eu-repo/semantics/acceptedVersion, doc-type:doctoralThesis, info:eu-repo/semantics/doctoralThesis, doc-type:Text |
| Rights | info:eu-repo/semantics/openAccess |
Page generated in 0.0021 seconds