The Drosophila Gr28bD product is a non-specific cation channel that can be used as a novel thermogenetic tool

Mishra, Aditi; Salari, Autoosa; Berigan, Benton R.; Miguel, Kayla; Amirshenava, Marzie; Robinson, Abbey O.; Zars, Benjamin C.; Lin, Jenna L.; Milescu, Lorin S.; Milescu, Mirela; Zars, Troy

doi:10.1038/s41598-017-19065-4

Cited by 12 publications

(28 citation statements)

References 34 publications

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“…Thus, the temperature sensitivity of Gr28bE might be limited to certain cell types. To measure the physiological changes underlying fly behavior, we co-expressed GR28bD or its orthologs with Gcamp6f in Drosophila motor neurons [9]. There were profound changes in Gr28bD induced neuronal activity with increase in temperature that could be measured as changes in Gcamp6f fluorescence.…”

Section: Discussionmentioning

confidence: 99%

“…or its thermosensitive orthologs function as non-selective cation channels that depolarize cells on activation ( [9], in prep). In addition to physiological studies, this observation also corroborates our hypothesis that hyperexcitability of neurons paralyzes flies with thermosensitive Gr overexpression.…”

Section: Discussionmentioning

confidence: 99%

“…With the use of one these novel tools we determined that place learning and memory is modulated by activity of dopaminergic neurons. Additionally, we have discussed our findings where we collaborated to quantify the physiological changes in neurons overexpressing these proteins [9] and study their functions in a heterologous system. The red edges indicate candidate thermosensitive GRs [69].…”

Section: Goals Of the Thesis: Aims And Rationalementioning

confidence: 99%

“…All behavior experiments were performed in the heat-box paradigm [9,87]. Briefly, activities of flies were observed as they walked the length of a small chamber which is lined on the top and bottom with Peltier elements.…”

Section: Behavioral Assaysmentioning

confidence: 99%

“…Since then, modifications of Golgi staining, use of viral vectors to trace development of circuits, GFP Reconstitution across Synaptic Partners (GRASP) to label specific synapses, and electron microscopy to identify microstructures have enabled thorough studies of brain anatomies in various organisms [1]. In the meantime, determining the functional connectivity of neural circuits has become feasible with the development of electrophysiology, optogenetics [2,3], chemogenetics (for example, DREADD) [4][5][6], thermogenetics [7][8][9], magnetothermogenetics [10,11] and imaging techniques such as FMRI [12].…”

Section: Introductionmentioning

confidence: 99%

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Identification, characterization and use of novel thermogenetic tools in drosophilia melanogaster

Mishra¹

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Extrinsic control of neural activity is necessary to decipher the neural mechanisms underlying behavior. Molecular tools that employ light (optogenetics) or temperature (thermogenetics) are primarily used for extrinsic manipulation of neurons. While the available tools offer precise temporal and spatial resolution, their caveats lie in the limited number of tools that can be used simultaneously to alter neuronal activity. The overlapping spectrum of activation of optogenetic tools prevents their simultaneous use in preparations. Similarly, the lack of thermogenetic tools that can function in the physiological range of organisms has restricted their use. The use of thermogenetic tools is limited to two members from the Transient receptor family of proteins, TrpA1 and TrpM8 to activate neurons, and one protein that reduces synaptic output, Shibirets. A major drawback to the Trp channels is their response to both temperature and voltage changes. Hence, the discovery of a new temperature sensitive Gustatory Receptor protein provided an opportunity to mine for other temperature sensitive proteins and develop novel thermogenetic tools. In this thesis we report the identification of several thermosensitive proteins, their characterization, and use in studying the learning and memory of freely moving flies. In the first chapter, we probed several Gustatory receptors for their temperature sensitivity using the heat box. The heat box is a high throughput system that enables us to test and track the behavior of single flies in response to temperature. The top and bottom of heat box chamber has Peltier elements that allow for control of temperature with a resolution of 1[degrees]C. We overexpressed several Gustatory receptors one at a time pan neuronally in Drosophila melanogaster and exposed them to various assays. Our initials results imply that at least 2 Drosophila melanogaster Gustatory receptors other than Gr28bD are temperature sensitive. To increase the repertoire of thermosensitive proteins, we assayed for temperature response properties of Gr28bD orthologs from 5 other Drosophila species that occupy different habitats in the world. We rationalized that flies in different habitats will have Gr28bD orthologs with unique temperature response properties designed to sustain in that habitat. Of the 5 proteins we tested, we found that 4 proteins are temperature sensitive at different temperatures. While pan-neuronal overexpression is a robust method to determine the temperature responsiveness of a protein, it does not recapitulate the natural environment the protein is present in. In D. melanogaster, Gr28bD is present in specialized heat sensing cells in the antenna, called Hot Cells. There are 3 Hot cells on each of the two antennae. There is however no physiological information on the where the orthologs are expressed. Since Gr28bD is used for rapid heat avoidance in flies, we rationalized that its orthologs too sever a similar function in their host species and are expressed in the peripheral regions. Hence, in the second chapter, we tested for the avoidance behavior of flies using two choice assays. We made mutant flies that lacked Gr28b proteins, including Gr28bD in the antennae. We then examined the ability of the orthologs to rescue the heat avoidance behavior in these mutants. We found that all the orthologs respond to temperature differences albeit, at different temperatures. Above a threshold temperature, flies rescued with some orthologs could not differentiate between small temperature differences, suggesting that the activity of the orthologs might saturate beyond certain temperatures. Some homologs responded to temperature only when expressed in Hot Cells, thus leading us to examine the presence of accessory proteins it the hot cells that might be enhancing the thermosensitive properties of these homologs. We found several candidate proteins that can studied further to determine their role in the temperature sensing in the hot cells. When used as thermogenetic tools, thermosensitive proteins are in localized environments in small cluster of cells. In the third chapter, we expressed Gr28bD in small clusters of dopaminergic neurons in the fly brain with an aim to understand the role of activation of dopaminergic neurons in operant place learning and memory paradigm. In addition to examining their learning scores at different temperatures, we investigated other behaviors of the flies during the training. Contrary to previous results from our lab that showed that dopaminergic neurons are not important for place learning and memory, we found that activation of a specific subset of dopaminergic neurons does alter place learning and memory. Our findings new laid the groundwork for more experiments to investigate dopaminergic modulation of place learning and memory.

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Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%