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1.
Proc Natl Acad Sci U S A ; 116(40): 20158-20168, 2019 10 01.
Artigo em Inglês | MEDLINE | ID: mdl-31527261

RESUMO

To assess the biological value of environmental stimuli, animals' sensory systems must accurately decode both the identities and the intensities of these stimuli. While much is known about the mechanism by which sensory neurons detect the identities of stimuli, less is known about the mechanism that controls how sensory neurons respond appropriately to different intensities of stimuli. The ionotropic receptor IR76b has been shown to be expressed in different Drosophila chemosensory neurons for sensing a variety of chemicals. Here, we show that IR76b plays an unexpected role in lowering the sensitivity of Drosophila sweet taste neurons. First, IR76b mutants exhibited clear behavioral responses to sucrose and acetic acid (AA) at concentrations that were too low to trigger observable behavioral responses from WT animals. Second, IR76b is expressed in many sweet neurons on the labellum, and these neurons responded to both sucrose and AA. Removing IR76b from the sweet neurons increased their neuronal responses as well as animals' behavioral responses to sucrose and AA. Conversely, overexpressing IR76b in the sweet neurons decreased their neuronal as well as animals' behavioral responses to sucrose and AA. Last, IR76b's response-lowering ability has specificity: IR76b mutants and WT showed comparable responses to capsaicin when the mammalian capsaicin receptor VR1 was ectopically expressed in their sweet neurons. Our findings suggest that sensitivity of Drosophila sweet neurons to their endogenous ligands is actively limited by IR76b and uncover a potential molecular target by which contexts can modulate sensitivity of sweet neurons.


Assuntos
Drosophila/fisiologia , Células Receptoras Sensoriais/fisiologia , Percepção Gustatória , Paladar , Animais , Biomarcadores , Mutação , Bulbo Olfatório , Limiar Gustativo
2.
J Neurogenet ; 35(3): 306-319, 2021 09.
Artigo em Inglês | MEDLINE | ID: mdl-33688796

RESUMO

Larval Drosophila are used as a genetically accessible study case in many areas of biological research. Here we report a fast, robust and user-friendly procedure for the whole-body multi-fluorescence imaging of Drosophila larvae; the protocol has been optimized specifically for larvae by systematically tackling the pitfalls associated with clearing this small but cuticularized organism. Tests on various fluorescent proteins reveal that the recently introduced monomeric infrared fluorescent protein (mIFP) is particularly suitable for our approach. This approach comprises an effective, low-cost clearing protocol with minimal handling time and reduced toxicity in the reagents employed. It combines a success rate high enough to allow for small-scale screening approaches and a resolution sufficient for cellular-level analyses with light sheet and confocal microscopy. Given that publications and database documentations typically specify expression patterns of transgenic driver lines only within a given organ system of interest, the present procedure should be versatile enough to extend such documentation systematically to the whole body. As examples, the expression patterns of transgenic driver lines covering the majority of neurons, or subsets of chemosensory, central brain or motor neurons, are documented in the context of whole larval body volumes (using nsyb-Gal4, IR76b-Gal4, APL-Gal4 and mushroom body Kenyon cells, or OK371-Gal4, respectively). Notably, the presented protocol allows for triple-color fluorescence imaging with near-infrared, red and yellow fluorescent proteins.


Assuntos
Animais Geneticamente Modificados , Imageamento Tridimensional/métodos , Imagem Óptica/métodos , Animais , Drosophila , Proteínas de Fluorescência Verde , Larva , Microscopia Confocal/métodos , Transgenes
3.
Cell Rep ; 18(3): 737-750, 2017 01 17.
Artigo em Inglês | MEDLINE | ID: mdl-28099851

RESUMO

Amino acid taste is expected to be a universal property among animals. Although sweet, bitter, salt, and water tastes have been well characterized in insects, the mechanisms underlying amino acid taste remain elusive. From a Drosophila RNAi screen, we identify an ionotropic receptor, Ir76b, as necessary for yeast preference. Using calcium imaging, we identify Ir76b+ amino acid taste neurons in legs, overlapping partially with sweet neurons but not those that sense other tastants. Ir76b mutants have reduced responses to amino acids, which are rescued by transgenic expression of Ir76b and a mosquito ortholog AgIr76b. Co-expression of Ir20a with Ir76b is sufficient for conferring amino acid responses in sweet-taste neurons. Notably, Ir20a also serves to block salt response of Ir76b. Our study establishes the role of a highly conserved receptor in amino acid taste and suggests a mechanism for mutually exclusive roles of Ir76b in salt- and amino-acid-sensing neurons.


Assuntos
Aminoácidos/farmacologia , Proteínas de Drosophila/metabolismo , Drosophila melanogaster/fisiologia , Receptores Ionotrópicos de Glutamato/metabolismo , Canais de Sódio/metabolismo , Paladar/efeitos dos fármacos , Animais , Animais Geneticamente Modificados/fisiologia , Sequência de Bases , Comportamento Animal/efeitos dos fármacos , Sistemas CRISPR-Cas/genética , Cálcio/metabolismo , Proteínas de Drosophila/antagonistas & inibidores , Proteínas de Drosophila/deficiência , Proteínas de Drosophila/genética , Drosophila melanogaster/efeitos dos fármacos , Feminino , Masculino , Microscopia Confocal , Neurônios/metabolismo , Neurônios/patologia , Fenótipo , Interferência de RNA , Receptores Ionotrópicos de Glutamato/antagonistas & inibidores , Receptores Ionotrópicos de Glutamato/genética , Canais de Sódio/genética , Cloreto de Sódio/farmacologia , Açúcares/farmacologia , Paladar/fisiologia
4.
Curr Biol ; 27(18): 2741-2750.e4, 2017 Sep 25.
Artigo em Inglês | MEDLINE | ID: mdl-28889974

RESUMO

Carboxylic acids are present in many foods, being especially abundant in fruits. Yet, relatively little is known about how acids are detected by gustatory systems and whether they have a potential role in nutrition or provide other health benefits. Here we identify sour gustatory receptor neurons (GRNs) in tarsal taste sensilla of Drosophila melanogaster. We find that most tarsal sensilla harbor a sour GRN that is specifically activated by carboxylic and mineral acids but does not respond to sweet- and bitter-tasting chemicals or salt. One pair of taste sensilla features two GRNs that respond only to a subset of carboxylic acids and high concentrations of salt. All sour GRNs prominently express two Ionotropic Receptor (IR) genes, IR76b and IR25a, and we show that both these genes are necessary for the detection of acids. Furthermore, we establish that IR25a and IR76b are essential in sour GRNs of females for oviposition preference on acid-containing food. Our investigations reveal that acids activate a unique set of taste cells largely dedicated to sour taste, and they indicate that both pH/proton concentration and the structure of carboxylic acids contribute to sour GRN activation. Together, our studies provide new insights into the cellular and molecular basis of sour taste.


Assuntos
Proteínas de Drosophila/genética , Drosophila melanogaster/fisiologia , Oviposição , Receptores Ionotrópicos de Glutamato/genética , Canais de Sódio/genética , Percepção Gustatória , Animais , Células Quimiorreceptoras/fisiologia , Proteínas de Drosophila/metabolismo , Drosophila melanogaster/genética , Feminino , Receptores Ionotrópicos de Glutamato/metabolismo , Canais de Sódio/metabolismo
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