GABAergic circuits control stimulus-instructed receptive field development in the optic tectum

Nat Neurosci. 2010 Sep;13(9):1098-106. doi: 10.1038/nn.2612. Epub 2010 Aug 8.

Abstract

During the development of sensory systems, receptive fields are modified by stimuli in the environment. This is thought to rely on learning algorithms that are sensitive to correlations in spike timing between cells, but the manner in which developing circuits selectively exploit correlations that are related to sensory inputs is unknown. We recorded from neurons in the developing optic tectum of Xenopus laevis and found that repeated presentation of moving visual stimuli induced receptive field changes that reflected the properties of the stimuli and that this form of learning was disrupted when GABAergic transmission was blocked. Consistent with a role for spike timing-dependent mechanisms, GABA blockade altered spike-timing patterns in the tectum and increased correlations between cells that would affect plasticity at intratectal synapses. This is a previously unknown role for GABAergic signals in development and highlights the importance of regulating the statistics of spiking activity for learning.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / drug effects
  • Action Potentials / physiology
  • Animals
  • GABA-A Receptor Antagonists
  • Larva
  • Motion
  • Motion Perception / drug effects
  • Motion Perception / physiology*
  • Neural Pathways / drug effects
  • Neural Pathways / growth & development
  • Neural Pathways / physiology
  • Neurons / drug effects
  • Neurons / physiology*
  • Patch-Clamp Techniques
  • Photic Stimulation
  • Receptors, GABA-A / metabolism
  • Signal Processing, Computer-Assisted
  • Superior Colliculi / drug effects
  • Superior Colliculi / growth & development*
  • Superior Colliculi / physiology*
  • Synaptic Transmission / drug effects
  • Synaptic Transmission / physiology
  • Time Factors
  • Xenopus laevis
  • gamma-Aminobutyric Acid / metabolism*

Substances

  • GABA-A Receptor Antagonists
  • Receptors, GABA-A
  • gamma-Aminobutyric Acid