scholarly journals Acid sensing by sweet and bitter taste neurons in Drosophila melanogaster

2013 ◽  
Vol 4 (1) ◽  
Author(s):  
Sandhya Charlu ◽  
Zev Wisotsky ◽  
Adriana Medina ◽  
Anupama Dahanukar
Keyword(s):  
Drosophila Melanogaster ◽  
Bitter Taste

scholarly journals Searching for relief: Drosophila melanogaster navigation in a virtual bitter maze

2019 ◽  
Author(s):  
Nicola Meda ◽  
Giovanni Frighetto ◽  
Aram Megighian ◽  
Mauro Agostino Zordan
Keyword(s):  
Drosophila Melanogaster ◽  
Pain Relief ◽  
Bitter Taste ◽  
Place Learning ◽  
Relevant Stimulus ◽  
Searching Behaviour ◽  
Safe Area ◽  
Visual Markers ◽  
Open Circular ◽  
Taste Stimulation

AbstractAnimals use pain-relief learning to discern which actions can diminish or abolish noxious stimuli. If relief from pain is provided in a specific location, place learning is the mechanism used to pinpoint that location in space. Little is known about how physiological and non-directly damaging stimuli can alter visual-based searching behaviour in animals. Here we show how the optogenetically-induced activation of bitter-sensing neurons urges Drosophila melanogaster to seek relief from bitter taste stimulation and that this distressful, but ecologically relevant stimulus, innately wired to the threat of intoxication, is sufficient to elicit pain-relief-like behavioural responses. Specifically, freely walking flies inside an open circular arena are trained to seek relief from the unpleasant stimulation by searching for a safe area alternatively positioned in the proximity of a pair of identical, diametrically opposed, visual markers. Moreover, and perhaps more importantly, under this paradigm flies develop visual place learning manifested by their seeking relief in the zone associated with bitter relief during the last trial of training, even when exposed to constant bitter stimulation with no relief provided. An important implication is that this form of learning does not lead to operant conditioning generalization. We further propose that kinematic indexes, such as the spatially-specific reduction of locomotor velocity, may provide immediate evidence of relief-based place learning and spatial memory.

Author response for "Location and arrangement of campaniform sensilla in Drosophila melanogaster"

2020 ◽  
Author(s):  
Gesa F. Dinges ◽  
Alexander S. Chockley ◽  
Till Bockemühl ◽  
Kei Ito ◽  
Alexander Blanke ◽  
...  
Keyword(s):  
Drosophila Melanogaster ◽  
Author Response ◽  
Campaniform Sensilla

Live Confocal Analysis of Fertilization and Early Development

2001 ◽  
Vol 7 (S2) ◽  
pp. 1012-1013
Author(s):  
Uyen Tram ◽  
William Sullivan
Keyword(s):  
Drosophila Melanogaster ◽  
Embryonic Development ◽  
Real Time ◽  
Early Development ◽  
Fluorescent Probes ◽  
Primary Defect ◽  
Fluorescent Analysis ◽  
Dynamic Event ◽  
Enormous Amount ◽  
Fluorescent Studies

Embryonic development is a dynamic event and is best studied in live animals in real time. Much of our knowledge of the early events of embryogenesis, however, comes from immunofluourescent analysis of fixed embryos. While these studies provide an enormous amount of information about the organization of different structures during development, they can give only a static glimpse of a very dynamic event. More recently real-time fluorescent studies of living embryos have become much more routine and have given new insights to how different structures and organelles (chromosomes, centrosomes, cytoskeleton, etc.) are coordinately regulated. This is in large part due to the development of commercially available fluorescent probes, GFP technology, and newly developed sensitive fluorescent microscopes. For example, live confocal fluorescent analysis proved essential in determining the primary defect in mutations that disrupt early nuclear divisions in Drosophila melanogaster. For organisms in which GPF transgenics is not available, fluorescent probes that label DNA, microtubules, and actin are available for microinjection.

Apoptosis and development

2003 ◽  
Vol 39 ◽  
pp. 11-24 ◽  
Author(s):  
Justin V McCarthy
Keyword(s):  
Drosophila Melanogaster ◽  
Mammalian Cells ◽  
Cell Number ◽  
Model Organisms ◽  
Biological Processes ◽  
Nematode Caenorhabditis Elegans ◽  
Apoptotic Pathway ◽  
Genetic Pathways ◽  
Evolutionarily Conserved ◽  
Multicellular Organisms

Apoptosis is an evolutionarily conserved process used by multicellular organisms to developmentally regulate cell number or to eliminate cells that are potentially detrimental to the organism. The large diversity of regulators of apoptosis in mammalian cells and their numerous interactions complicate the analysis of their individual functions, particularly in development. The remarkable conservation of apoptotic mechanisms across species has allowed the genetic pathways of apoptosis determined in lower species, such as the nematode Caenorhabditis elegans and the fruitfly Drosophila melanogaster, to act as models for understanding the biology of apoptosis in mammalian cells. Though many components of the apoptotic pathway are conserved between species, the use of additional model organisms has revealed several important differences and supports the use of model organisms in deciphering complex biological processes such as apoptosis.

Insights into amyloid disease from fly models

2014 ◽  
Vol 56 ◽  
pp. 69-83 ◽  
Author(s):  
Ko-Fan Chen ◽  
Damian C. Crowther
Keyword(s):  
Drosophila Melanogaster ◽  
Neurodegenerative Disorders ◽  
Amyloid Β ◽  
Amyloid Β Peptide ◽  
Disease Pathogenesis ◽  
Amyloid Aggregates ◽  
Aβ Amyloid ◽  
Polypeptide Chains ◽  
Amyloid Diseases

The formation of amyloid aggregates is a feature of most, if not all, polypeptide chains. In vivo modelling of this process has been undertaken in the fruitfly Drosophila melanogaster with remarkable success. Models of both neurological and systemic amyloid diseases have been generated and have informed our understanding of disease pathogenesis in two main ways. First, the toxic amyloid species have been at least partially characterized, for example in the case of the Aβ (amyloid β-peptide) associated with Alzheimer's disease. Secondly, the genetic underpinning of model disease-linked phenotypes has been characterized for a number of neurodegenerative disorders. The current challenge is to integrate our understanding of disease-linked processes in the fly with our growing knowledge of human disease, for the benefit of patients.

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