Journal of Neuroscience · 2011 · 27 citations · 19 references
Life SciencesNeurobiologyNeuroscienceCellular NeurobiologyDevelopmental NeuroscienceNeurophysiologyGabaergic SignalingNeural DevelopmentNeurotransmissionRetinal DevelopmentRetinal NeurobiologySynaptic TransmissionHomeostatic AdaptationMultielectrode Array TechnologyRetinal Circuit DynamicsRetinal Ganglion Cell Firing PatternsRetinal HyperpolarizationRetinal Oscillatory ActivityRetinal WavesSpontaneous Retinal Activity
Developing retinal ganglion cells fire in correlated spontaneous bursts, resulting in propagating waves with robust spatiotemporal features preserved across development and species. Here we investigate the effects of homeostatic adaptation on the circuits controlling retinal waves. Mouse retinal waves were recorded in vitro for up to 35 h with a multielectrode array in presence of the GABA(A) antagonist bicuculline, allowing us to obtain a precise, time-resolved characterization of homeostatic effects in this preparation. Experiments were performed at P4-P6, when GABA(A) signaling is depolarizing in ganglion cells, and at P7-P10, when GABA(A) signaling is hyperpolarizing. At all ages, bicuculline initially increased the wave sizes and other activity metrics. At P5-P6, wave sizes decreased toward control levels within a few hours while firing remained strong, but this ability to compensate disappeared entirely from P7 onwards. This demonstrates that homeostatic control of spontaneous retinal activity maintains specific network dynamic properties in an age-dependent manner, and suggests that the underlying mechanism is linked to GABA(A) signaling.
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Activity-dependent scaling of quantal amplitude in neocortical neurons
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Synchronous Bursts of Action Potentials in Ganglion Cells of the Developing Mammalian Retina
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Medicine, Neurobiology, Neuroscience +17
Anu Bansal, Joshua H. Singer, Bryan J. Hwang et al. · Journal of Neuroscience · 2000 · 354 citations · Full text