Big Lessons from Tiny Flies: Drosophila melanogaster as a Model to Explore Dysfunction of Dopaminergic and Serotonergic Neurotransmitter Systems.
Ameya Sanjay KastureThomas HummelSonja SucicMichael FreissmuthPublished in: International journal of molecular sciences (2018)
The brain of Drosophila melanogaster is comprised of some 100,000 neurons, 127 and 80 of which are dopaminergic and serotonergic, respectively. Their activity regulates behavioral functions equivalent to those in mammals, e.g., motor activity, reward and aversion, memory formation, feeding, sexual appetite, etc. Mammalian dopaminergic and serotonergic neurons are known to be heterogeneous. They differ in their projections and in their gene expression profile. A sophisticated genetic tool box is available, which allows for targeting virtually any gene with amazing precision in Drosophila melanogaster. Similarly, Drosophila genes can be replaced by their human orthologs including disease-associated alleles. Finally, genetic manipulation can be restricted to single fly neurons. This has allowed for addressing the role of individual neurons in circuits, which determine attraction and aversion, sleep and arousal, odor preference, etc. Flies harboring mutated human orthologs provide models which can be interrogated to understand the effect of the mutant protein on cell fate and neuronal connectivity. These models are also useful for proof-of-concept studies to examine the corrective action of therapeutic strategies. Finally, experiments in Drosophila can be readily scaled up to an extent, which allows for drug screening with reasonably high throughput.
Keyphrases
- drosophila melanogaster
- genome wide
- spinal cord
- endothelial cells
- copy number
- high throughput
- cell fate
- genome wide identification
- induced pluripotent stem cells
- resting state
- white matter
- pluripotent stem cells
- dna methylation
- physical activity
- oxidative stress
- functional connectivity
- weight loss
- machine learning
- binding protein
- spinal cord injury
- multiple sclerosis
- sleep quality
- genome wide analysis
- blood brain barrier