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Original Article

Developmental Changes of GABA Synaptic Transient in Cerebellar Granule Cells

Department of Physiology and Biophysics, Georgetown University School of Medicine, Washington, DC (A.B., C.L., S.V., J.W.M.); and Laboratory of Neuroscience, Department of Biophysics, Wroclaw Medical University, Wroclaw, Poland (J.W.M.)

Abstract

The time course of synaptic currents is largely determined by the microscopic gating of the postsynaptic receptors and the temporal profile of the synaptic neurotransmitter concentration. Although several lines of evidence indicate that developmental changes of GABAergic synaptic current time course are clearly correlated with a switch in postsynaptic receptors, much less is known about the modification of GABA release during development. To address this issue, we studied the sensitivity of miniature inhibitory postsynaptic currents (mIPSCs) to a quickly dissociating competitive antagonist, 1,2,5,6-tetrahydropyridine-4-yl)methylphosphinic acid (TPMPA), in neurons cultured for 6 to 8 days in vitro (DIV) ("young") and for 12 to 14 DIV ("old"). mIPSCs recorded in young neurons were significantly more resistant to the block by TPMPA. This observation was interpreted as a consequence of a more efficient displacement of TPMPA from GABA_A receptors caused by a stronger GABA release in young neurons. The change in mIPSC sensitivity to TPMPA during development was not affected by the deletion of ₁ subunit, supporting its presynaptic origin. The effects of a second quickly dissociating antagonist, SR-95103 [2-(carboxy-3'-propyl)-3-amino-4-methyl-6-phenylpyridazinium chloride], on young, old, and ₁ -/- neurons were qualitatively the same as those obtained with TPMPA. Moreover, the analysis of current responses to ultrafast GABA applications showed that the unbinding rates of TPMPA in DIV 6 to 8 and in DIV 12 to 14 neurons are not significantly different, ruling out the postsynaptic mechanism of differential TPMPA action. Thus, we provide evidence that presynaptic GABA uniquantal release is developmentally regulated.

Address correspondence to: Dr. Andrea Barberis, Department of Physiology and Biophysics, Georgetown University School of Medicine, 225 Basic Research Bldg. 3900 Reservoir Rd., NW, Washington, DC 20007. E-mail: barberis{at}sissa.it

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				J. Szabadics, G. Tamas, and I. Soltesz Different transmitter transients underlie presynaptic cell type specificity of GABAA,slow and GABAA,fast PNAS, September 11, 2007; 104(37): 14831 - 14836. [Abstract] [Full Text] [PDF]