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Title page for ETD etd-03312010-103304


Type of Document Dissertation
Author Tang, Xin
Author's Email Address xin.tang@vanderbilt.edu
URN etd-03312010-103304
Title MODULATION OF GABAA RECEPTOR FUNCTION BY PKA AND PKC PROTEIN PHOSPHORYLATION
Degree PhD
Department Neuroscience
Advisory Committee
Advisor Name Title
Roger J. Colbran Committee Chair
Albert H. Beth Committee Member
Alfred L. George Committee Member
Robert L. Macdonald Committee Member
Keywords
  • GABAA receptor
  • phosphorylation
  • PKA
  • PKC
Date of Defense 2010-03-12
Availability unrestricted
Abstract
We studied the modulation of 432L and 43 GABAA receptor currents by two protein kinases, PKA and PKC. Although modulation of synaptic 1¦2 GABAA receptor isoforms has been studied widely, study of the modulation of peri- and extrasynaptic ¦ and non-synaptic ¦ GABAA receptors by protein phosphorylation is lacking. Using patch-clamp recording, we compared the effects of protein phosphorylation of 432L and 43 GABAA receptors under different levels of activation that included spontaneous openings, tonic currents activated by low GABA concentrations and phasic currents activated by high GABA concentrations. We found that PKA-activation preferentially increased spontaneous 43 receptor currents by increasing single channel open frequency and decreased GABA-activated steady-state, tonic 43 currents, but only had small effects on spontaneous and GABA-activated tonic 432L currents, indicating the differential modulation of tonic inhibition mediated by 432L and 43 GABAA receptors. In contrast, both PKA and PKC had similar effects on desensitization of phasic 432L and 43 currents, implying a common modulatory mechanism of protein phosphorylation in regulating synaptic current kinetics. Our study suggested that protein phosphorylation had profound effects on different GABAA receptor isoforms, which should also be determined by receptor sub-cellular (synaptic or non-synaptic) localization and by the level of ambient GABA (spontaneous or GABA-activated), thus ensuring precise modulation of specific GABAA receptor properties in specific brain areas.
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