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The Journal of Neuroscience, December 13, 2006, 26(50):12996-13006; doi:10.1523/JNEUROSCI.3503-06.2006
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Cellular/Molecular
AMPA/Kainate Receptors Drive Rapid Output and Precise Synchrony in Olfactory Bulb Granule Cells
Nathan E. Schoppa
Department of Physiology and Biophysics, University of Colorado at Denver Health Sciences Center at Fitzsimons, Aurora, Colorado 80045
Correspondence should be addressed to Nathan E. Schoppa, Department of Physiology and Biophysics, University of Colorado at Denver Health Sciences Center at Fitzsimons, Mail Stop 8307, P.O. Box 6511, Aurora, CO 80045. Email: Nathan.Schoppa{at}UCHSC.edu
Gamma frequency (3070 Hz) synchronized oscillatory activity in the olfactory bulb is widely believed to be important for odor detection and discrimination. As in other circuits with "gamma activity," the activity in the bulb is driven by GABAergic interneurons, specifically a class of axonless cells called granule cells. However, bulb granule cells appear to lack some key mechanistic features that promote rapid synchrony in other circuits, including direct electrical interconnections and dominant actions for fast neurotransmitter receptors. At least under "static" stimulus conditions, granule cells are driven by kinetically slow NMDA receptors. Here, I used patch-clamp recordings in rat olfactory bulb slices to better understand mechanisms that shape granule cell activity under "dynamic" stimulus conditions that mimic a natural odor stimulus. During a 4 Hz patterned stimulation of olfactory nerve afferents, activation of single granule cells was primarily controlled by two classes of AMPA/kainate receptor-mediated synaptic inputs derived from output mitral cells. The rapid kinetics of these receptors, together with inactivation of A-type potassium channels, ensured that granule cells had short spike-response times. Studies in cell pairs, moreover, indicated that excitatory inputs could synchronize granule cells on a rapid time scale (25 ms), in turn resulting in phase-locked GABA release onto mitral cells. The precision of granule cell synchrony was controlled by the same biophysical mechanisms that promoted rapid single-cell spiking. These studies demonstrate the mechanistic underpinnings that transform a circuit with slow, uncoupled activity under static conditions into a fast, dynamic circuit operating with high precision under physiological conditions.
Key words: olfactory; synchronization; AMPA receptor; GABAergic; interneuron; mitral cell; granule cell
Received Aug. 12, 2006;
revised Nov. 7, 2006;
accepted Nov. 7, 2006.
Correspondence should be addressed to Nathan E. Schoppa, Department of Physiology and Biophysics, University of Colorado at Denver Health Sciences Center at Fitzsimons, Mail Stop 8307, P.O. Box 6511, Aurora, CO 80045. Email: Nathan.Schoppa{at}UCHSC.edu
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