Biomedical subjects

Barry G Condron

Publications and source records attributed to Barry G Condron.

4 recordsLinked to original sources

PubMed2005

Development and sensitivity to serotonin of Drosophila serotonergic varicosities in the central nervous system.

Serotonin is a classical small-molecule neurotransmitter with known effects on developmental processes. Previous studies have shown a developmental role for serotonin in the fly peripheral nervous system. In this study, we show that serotonin can modulate the development of serotonergic varicosities within the fly central nervous system. We have developed a system to examine the development of serotonergic varicosities in the larval CNS. We use this method to describe the normal serotonergic development in the A7 abdominal ganglion. From first to third instar larvae, the volume of the neuropil and number of serotonergic varicosities increase substantially while the varicosity density remains relatively constant. We hypothesize that serotonin is an autoregulator for serotonergic varicosity density. We tested the sensitivity of serotonergic varicosities to serotonin by adding neurotransmitter at various stages to isolated larval ventral nerve cords. Addition of excess exogenous serotonin decreases native varicosity density in older larvae, and these acute effects are reversible. The effects of serotonin appear to be selective for serotonergic varicosities, as dopaminergic and corazonergic varicosities remain qualitatively intact following serotonin application.

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PubMed2005

An assay of behavioral plasticity in Drosophila larvae.

Stress, or threats to homeostasis, is a universal part of life. Organisms face changing and challenging situations everyday, and the ability to respond to such stress is essential for survival. When subjected to acute stress, the body responds molecularly and behaviorally in order to recover a steady state. We developed a simple and robust assay of behavioral plasticity for Drosophila larvae in which well-defined behavioral responses and recovery can be observed and quantified. After experiencing different control and bright light treatments, populations of photophobic fly larvae were placed a defined distance from a food source to which they crawled. Half-times (t(1/2)), or times at which half the total number of larvae reached the food, were used to compare different treatments and larval populations. Repeated control treatments with a main experimental strain gave tight, reproducible t(1/2) ranges. Control treatments with the wild type strains Oregon R and Canton S, the "rover" and "sitter" alleles of the forager locus, and eyeless mutants gave comparable results to those of the experimental strain. Exposure to bright light for a defined time period resulted in a reproducible slowing of locomotion. However, given a defined recovery period, the larvae recover full, normal locomotion. In addition, bright light treatments with Canton S gave comparable results to those of the experimental strain. Eyeless mutants, which are partially blind, do not show a response to bright light treatment. Thus, our assay measures the behavioral responses to bright light in Drosophila larvae and therefore might be useful as a general assay for studying behavioral plasticity and, potentially, adaptation to a stressful stimulus.

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PubMed2004

Variation in serotonergic and dopaminergic neuronal survival in the central nervous system of adult Drosophila.

Loss of serotonergic and dopaminergic neurons may have serious implications for normal brain function. Drosophila models of neurodegenerative diseases utilize the short life-span and simple anatomy of the fly to characterize the molecular and genetic processes characteristic of each dysfunctional state. In fly embryonic and larval ventral nerve cords, serotonergic and dopaminergic neurons are positioned in a stereotypic pattern that is reorganized during metamorphosis. In this study, we examine the adult pattern of serotonergic and dopaminergic neurons within the adult fly ventral nerve cord. We find that the number of cells lost following metamorphosis is highly variable. Changes in cell number attributable to age are therefore likely to be highly masked by developmental variation. The source of this variation is probably apoptosis-based cell loss during pupal development.

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PubMed2004

robo2 and robo3 interact with eagle to regulate serotonergic neuron differentiation.

The function of the central nervous system (CNS) depends crucially upon the correct differentiation of neurons and formation of axonal connections. Some aspects of neuronal differentiation are known to occur as axonal connections are forming. Although serotonin is a highly conserved neurotransmitter that is important for many CNS functions, little is known about the process of serotonergic neuron differentiation. We show that in Drosophila, expression of the serotonin transporter (SerT) is both temporally and physically related to midline crossing. Additionally, we show that the axon guidance molecules roundabout2 and roundabout3 (robo2/3) are necessary for serotonergic neuron differentiation and function independently of their ligand, slit. Loss of robo2 or robo3 causes a loss of SerT expression in about half of neurons, and resembles the phenotype seen in mutants for the transcription factor eagle (eg). Finally, we show a direct relationship between robo2/3 and eg: robo2/3 mutants lose Eg expression in serotonergic neurons, and robo2 and eg interact genetically to regulate SerT expression. We propose that post-midline expression of Robo2/3 is part of a signal that regulates serotonergic neuron differentiation and is transduced by the transcription factor Eg.

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