Our laboratory is interested in how heightened sensory drive competes for representation through cortical reorganization
that displaces or overlays existing functional sensory cortex. In the somatosensory system, heightened use or "over-use" of
a particular part of the skin will reassign neurons from neighboring representations of the body map to the region with
increased touch rates. Our experiments are conducted in mice that have been subjected to a tactile over-stimulation behavioral
task. We examine competition-based cortical reorganization from three perspectives:
First, we use electrophysiology to explore and characterize how the reassignment of cortical tissue alters firing patterns.
We record from isolated units with multi-electrode arrays in anesthetized, awake restrained, or awake/behaving animals in order
to define the extent of reorganization as a function of training time, as well as the functional specificity of re-wiring. We
are particularly interested in understanding how the reorganization process respectively augments or impairs the responsiveness
of neurons to new tactile input versus responsiveness to its former areas.
Second, we use pharmacological approaches to establish the degree to which reorganization plugs in new connectivity, rewires
existing connectivity and/or abolishes older connections. To explore the full range of functioning pre- and post-reorganization
circuitry we use microiontophoresis to locally administer pharmacological agents directed at a number of neurotransmitter systems.
We are specifically interested in identifying how neuromodulators may re-weight sensory drive from different body regions in the
acute state, once reorganization has been established, to reveal its new tactile responsiveness or the original
developmentally-regulated identity assignment of that neuron.
Third, we use molecular biology along with electrophysiology in wild type and transgenic animals to identify biochemical and
genetic mechanisms that drive and stabilize these changes. We are interested in understanding exactly which biochemical and genetic
mechanisms cue the system to undergo experience-dependent changes. Earlier work by our group has shown a role for candidate plasticity
genes in the cortical response to enriched sensory environments. We are interested in how the pathways that drive the expression of
candidate-plasticity genes along, with their downstream targets, may initiate and/or stabilize the new firing properties of neurons in
the reorganized somatosensory cortices.
Pinaud, R, Tremere, LA & De Weerd, P (Eds.) Plasticity in the Visual System: From Genes to Circuits. Springer-Verlag, New York
(2005). ISBN: 0-387-28189-4.
Pinaud, R & Tremere, LA (Eds.) Immediate Early Genes in Sensory Processing, Cognitive Performance and Neurological Disorders.
Springer-Verlag, New York (2006). ISBN: 0-387-33603-6.
SELECTED PEER-REVIEWED PUBLICATIONS
Tremere, LA & Pinaud, R (2006). Disparity for disinhibitory and excitatory effects during cortical reorganization. Int.
J. Neurosci. 116: 547-564.
Tremere, LA & Pinaud, R (2005). Incongruent restoration of inhibitory transmission and general metabolic activity during
reorganization of somatosensory cortex. Int. J. Neurosci. 115: 1025-1037.
Palmer, MJ, Taschenberger, H, Hull, C, Tremere, L & von Gersdorff, H (2003). Synaptic activation of presynaptic glutamate
transporter currents in a ribbon-type but not in a conventional active zone nerve terminal. J. Neurosci. 23: 4831-4841.
Pinaud, R, Tremere, LA, Penner, MR, Hess, FF, Barnes, SA, Robertson, HA & Currie, RW (2002). Plasticity-driven gene expression
in the rat retina. Mol. Brain Res. 98: 93-101.
Tremere, L, Hicks, TP & Rasmusson, DD (2001). Role of inhibition in cortical reorganization of the adult raccoon revealed by
microiontophoretic blockade of GABA-A receptors. J. Neurophysiol. 86: 94-103.
Tremere, L, Hicks, TP & Rasmusson, DD (2001). Control of receptive field size by GABA-A receptors in reorganizing somatosensory
cortex. Exp. Brain Res. 136: 447-455.
Pinaud, R, Tremere, L and Penner, MR (2000). Light-induced zif268 expression is dependent on noradrenergic input in rat visual
cortex. Brain Res. 882: 251-255.
SELECTED BOOK CHAPTERS
Pinaud, R, Terleph, TA, Currie, RW & Tremere, LA (2006). Regulation of Immediate Early Genes in the Visual Cortex. In: Immediate
Early Genes in Sensory Processing, Cognitive Performance and Neurological Disorders. R. Pinaud and L.A. Tremere (Eds.), Springer-Verlag,
New York. Chapter 2, pp 13-33.
Pinaud, R, Filipkowski, R, Fortes, AF & Tremere, LA (2006). Immediate Early Gene Expression in the Primary Somatosensory Cortex:
Focus on the Barrel Cortex. In: Immediate Early Genes in Sensory Processing, Cognitive Performance and Neurological Disorders. R. Pinaud
and L.A. Tremere (Eds.), Springer-Verlag, New York. Chapter 5, pp 73-92.
Pinaud, R, Terleph, TA & Tremere, LA (2005). Neuromodulatory Transmitters in Sensory Processing and Plasticity in the Primary Visual
Cortex. In: Plasticity in the Visual System: From Genes to Circuits. R. Pinaud, LA Tremere and P. De Weerd (Eds.), Springer-Verlag, New York.
Chapter 7, pp 127-151.
Tremere, LA & Pinaud, R (2005). Intra-Cortical Inhibition in the Regulation of Receptive Field Properties and Neural Plasticity in
the Primary Visual Cortex. In: Plasticity in the Visual System: From Genes to Circuits. R. Pinaud, LA Tremere and P. De Weerd (Eds.),
Springer-Verlag, New York. Chapter 11, pp 229-243.
Tremere, LA, De Weerd, P & Pinaud, R (2005). A Unified Theoretical Framework for Plasticity in Visual Circuitry. In: Plasticity in
the Visual System: From Genes to Circuits. R. Pinaud, LA Tremere and P. De Weerd (Eds.), Springer-Verlag, New York. Chapter 16, pp 347-355.
Tremere, LA, Pinaud, R & De Weerd, P (2003). Contributions of Inhibitory Mechanisms to Perceptual Completion and Cortical Reorganization.
In: Filling-in: From Perceptual Completion to Cortical Reorganization. L. Pessoa and P. De Weerd (Eds.), Oxford University Press, San Francisco.
Chapter 15, pp 295-322.