Show simple item record

dc.contributor.advisorOland, Lynneen
dc.contributor.authorCHARLTON, JULIE ANN
dc.creatorCHARLTON, JULIE ANNen
dc.date.accessioned2016-06-11T01:17:11Z
dc.date.available2016-06-11T01:17:11Z
dc.date.issued2016
dc.identifier.citationCHARLTON, JULIE ANN. (2016). NEURAL ACTIVITY AFFECTS ASTROCYTE MORPHOLOGY IN DROSOPHILA MELANOGASTER (Bachelor's thesis, University of Arizona, Tucson, USA).
dc.identifier.urihttp://hdl.handle.net/10150/612643
dc.description.abstractAstrocytes are known to maintain a proper ionic balance in the central nervous system, take up neurotransmitters after synaptic signaling, and modulate synaptic activity through a reciprocal conversation in which neuronal activity induces responses in glial cells that, in turn, modulate neuronal activity. We previously reported that constitutive RNAi knockdown of the GABA transporter in astrocyte--‐like glia of the 3rd--‐instar ventral nerve cord (VNC) strongly reduced larval locomotion, indicating that altering astrocyte function modulates activity in neurons comprising the motor circuitry (MacNamee et al., SfN abstract 2013). Here we have manipulated neural activity in the larva to assess the impact of altered neuronal activity on astrocytes. We fed larvae picrotoxin, which blocks GABAA receptors and glutamate--‐gated chloride channels and used a FLP--‐out genetic construct to visualize the detailed morphology of astrocytes in the VNC. Results to date indicate that the pharmacological treatment, which would be expected to change the balance of inhibition and excitation, significantly reduced locomotor activity and concomitantly led to a marked decrease in the volume occupied by the branching processes of astrocytes. The impact on glial morphology is being assessed using 3--‐D reconstructions of high--‐magnification confocal microscopic images.
dc.language.isoen_USen
dc.publisherThe University of Arizona.en
dc.rightsCopyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.en
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.titleNEURAL ACTIVITY AFFECTS ASTROCYTE MORPHOLOGY IN DROSOPHILA MELANOGASTERen_US
dc.typetexten
dc.typeElectronic Thesisen
thesis.degree.grantorUniversity of Arizonaen
thesis.degree.levelBachelorsen
thesis.degree.disciplineHonors Collegeen
thesis.degree.disciplineNeuroscience and Cognitive Scienceen
thesis.degree.nameB.S.en
refterms.dateFOA2018-09-11T12:36:03Z
html.description.abstractAstrocytes are known to maintain a proper ionic balance in the central nervous system, take up neurotransmitters after synaptic signaling, and modulate synaptic activity through a reciprocal conversation in which neuronal activity induces responses in glial cells that, in turn, modulate neuronal activity. We previously reported that constitutive RNAi knockdown of the GABA transporter in astrocyte--‐like glia of the 3rd--‐instar ventral nerve cord (VNC) strongly reduced larval locomotion, indicating that altering astrocyte function modulates activity in neurons comprising the motor circuitry (MacNamee et al., SfN abstract 2013). Here we have manipulated neural activity in the larva to assess the impact of altered neuronal activity on astrocytes. We fed larvae picrotoxin, which blocks GABAA receptors and glutamate--‐gated chloride channels and used a FLP--‐out genetic construct to visualize the detailed morphology of astrocytes in the VNC. Results to date indicate that the pharmacological treatment, which would be expected to change the balance of inhibition and excitation, significantly reduced locomotor activity and concomitantly led to a marked decrease in the volume occupied by the branching processes of astrocytes. The impact on glial morphology is being assessed using 3--‐D reconstructions of high--‐magnification confocal microscopic images.


Files in this item

Thumbnail
Name:
azu_etd_mr_2016_0035_sip1_m.pdf
Size:
1.899Mb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record