the clock input to the first optic neuropil of drosophila melanogaster expressing neuronal circadian plasticity时钟输入的第一视觉神经纤维网黑腹果蝇表达神经生理可塑性.pdfVIP
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the clock input to the first optic neuropil of drosophila melanogaster expressing neuronal circadian plasticity时钟输入的第一视觉神经纤维网黑腹果蝇表达神经生理可塑性
The Clock Input to the First Optic Neuropil of Drosophila
melanogaster Expressing Neuronal Circadian Plasticity
Milena Damulewicz, Elzbieta Pyza*
Department of Cell Biology and Imaging, Institute of Zoology, Jagiellonian University, Krakow, Poland
Abstract
In the first optic neuropil (lamina) of the fly’s visual system, two interneurons, L1 and L2 monopolar cells, and epithelial glial
cells show circadian rhythms in morphological plasticity. These rhythms depend on clock gene period (per) and
cryptochrome (cry) expression. In the present study, we found that rhythms in the lamina of Drosophila melanogaster may be
regulated by circadian clock neurons in the brain since the lamina is invaded by one neurite extending from ventral lateral
neurons; the so-called pacemaker neurons. These neurons and the projection to the lamina were visualized by green
fluorescent protein (GFP). GFP reporter gene expression was driven by the cry promotor in cry-GAL4/UAS-GFP transgenic
lines. We observed that the neuron projecting to the lamina forms arborizations of varicose fibers in the distal lamina. These
varicose fibers do not form synaptic contacts with the lamina cells and are immunoreactive to the antisera raised against a
specific region of Schistocerca gregaria ion transport peptide (ITP). ITP released in a paracrine way in the lamina cortex, may
regulate the swelling and shrinking rhythms of the lamina monopolar cells and the glia by controlling the transport of ions
and fluids across cell membranes at particular times of the day.
Citation: Damulewicz M, Pyza E (2011) The Clock Input to the First Optic Neuropil of Drosophila melanogaster Expressing Neuronal Circadian Plasticity. PLoS
ONE 6(6): e21258. doi:10.1371/journal.pone.0021258
Editor: Efthimios M. C. Skoulakis, Alexander Flemming Biomedical Sciences Research Center, Greece
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