Nonsynaptic Glycine Receptor Activation during Early Neocortical Development

• Published in: Neuron (Cambridge, Mass.) Mass.), 1998, Vol.20 (1), p.43-53
• Main Authors: Flint, Alexander C, Liu, Xiaolin, Kriegstein, Arnold R
• Format: Article
• Language: English
• Subjects: Aging - metabolism; Animals; Animals, Newborn - growth & development; Animals, Newborn - metabolism; Calcium - metabolism; Cerebral Cortex - embryology; Cerebral Cortex - growth & development; Cerebral Cortex - metabolism; dysgenesis; Embryo, Mammalian - metabolism; Embryonic and Fetal Development - physiology; Intracellular Membranes - metabolism; Ligands; Neurons - physiology; Osmolar Concentration; Rats; Rats, Sprague-Dawley; Receptors, Glycine - metabolism; Receptors, Glycine - physiology; Synapses - metabolism; taurine; Taurine - metabolism
• ISSN: 0896-6273; 1097-4199
• DOI: 10.1016/S0896-6273(00)80433-X

Glycine receptors (GlyRs) contribute to fast inhibitory synaptic transmission in the brain stem and spinal cord. GlyR subunits are expressed in the developing neocortex, but a neurotransmitter system involving cortical GlyRs has yet to be demonstrated. Here, we show that GlyRs in immature neocortex are excitatory and activated by a nonsynaptically released endogenous ligand. Of the potential ligands for cortical GlyRs, taurine is by far the most abundant in the developing neocortex. We found that taurine is stored in immature cortical neurons and that manipulations known to elevate extracellular taurine cause GlyR activation. These data indicate that nonsynaptically released taurine activates GlyRs during neocortical development. As fetal taurine deprivation can cause cortical dysgenesis, it is possible that taurine influences neocortical development by activating GlyRs.