Increasing Spontaneous Retinal Activity before Eye Opening Accelerates the Development of Geniculate Receptive Fields

Visually evoked activity is necessary for the normal development of the visual system. However, little is known about the capacity for patterned spontaneous activity to drive the maturation of receptive fields before visual experience. Retinal waves provide instructive retinotopic information for the anatomical organization of the visual thalamus. To determine whether retinal waves also drive the maturation of functional responses, we increased the frequency of retinal waves pharmacologically in the ferret (Mustela putorius furo) during a period of retinogeniculate development before eye opening. The development of geniculate receptive fields after receiving these increased neural activities was measured using single-unit electrophysiology. We found that increased retinal waves accelerate the developmental reduction of geniculate receptive field sizes. This reduction is due to a decrease in receptive field center size rather than an increase in inhibitory surround strength. This work reveals an instructive role for patterned spontaneous activity in guiding the functional development of neural circuits. SIGNIFICANCE STATEMENT Patterned spontaneous neural activity that occurs during development is known to be necessary for the proper formation of neural circuits. However, it is unknown whether the spontaneous activity alone is sufficient to drive the maturation of the functional properties of neurons. Our work demonstrates for the first time an acceleration in the maturation of neural function as a consequence of driving patterned spontaneous activity during development. This work has implications for our understanding of how neural circuits can be modified actively to improve function prematurely or to recover from injury with guided interventions of patterned neural activity.

[1]  Na Liu,et al.  Early Natural Stimulation through Environmental Enrichment Accelerates Neuronal Development in the Mouse Dentate Gyrus , 2012, PloS one.

[2]  Colin J. Akerman,et al.  Visual Experience before Eye-Opening and the Development of the Retinogeniculate Pathway , 2002, Neuron.

[3]  L. Chalupa,et al.  Epibatidine application in vitro blocks retinal waves without silencing all retinal ganglion cell action potentials in developing retina of the mouse and ferret. , 2008, Journal of neurophysiology.

[4]  A. Huberman,et al.  Ephrin-As mediate targeting of eye-specific projections to the lateral geniculate nucleus , 2005, Nature Neuroscience.

[5]  Marla B Feller,et al.  Extrasynaptic glutamate and inhibitory neurotransmission modulate ganglion cell participation during glutamatergic retinal waves. , 2013, Journal of neurophysiology.

[6]  Retinal waves regulate afferent terminal targeting in the early visual pathway , 2015, Proceedings of the National Academy of Sciences.

[7]  B. Chapman Necessity for afferent activity to maintain eye-specific segregation in ferret lateral geniculate nucleus. , 2000, Science.

[8]  Daniel Kerschensteiner,et al.  A Precisely Timed Asynchronous Pattern of ON and OFF Retinal Ganglion Cell Activity during Propagation of Retinal Waves , 2008, Neuron.

[9]  R. Reid,et al.  Diverse receptive fields in the lateral geniculate nucleus during thalamocortical development , 2000, Nature Neuroscience.

[10]  S. Bisti,et al.  Blockade of Glutamate-Mediated Activity in the Developing Retina Perturbs the Functional Segregation of ON and OFF Pathways , 1998, The Journal of Neuroscience.

[11]  J. Movshon,et al.  Behavioral/Systems/Cognitive Functional Maturation of the Macaque’s Lateral Geniculate Nucleus , 2004 .

[12]  Alessandro Sale,et al.  Enriched experience and recovery from amblyopia in adult rats: Impact of motor, social and sensory components , 2012, Neuropharmacology.

[13]  M. Crair,et al.  An Instructive Role for Patterned Spontaneous Retinal Activity in Mouse Visual Map Development , 2011, Neuron.

[14]  B. Winblad,et al.  Increased expression of brain-derived neurotrophic factor mRNA in rat hippocampus is associated with improved spatial memory and enriched environment , 1992, Neuroscience Letters.

[15]  John B. Troy,et al.  Non-Centered Spike-Triggered Covariance Analysis Reveals Neurotrophin-3 as a Developmental Regulator of Receptive Field Properties of ON-OFF Retinal Ganglion Cells , 2010, PLoS Comput. Biol..

[16]  C. Shatz,et al.  Competition in retinogeniculate patterning driven by spontaneous activity. , 1998, Science.

[17]  D A Butts,et al.  The Information Content of Spontaneous Retinal Waves , 2001, The Journal of Neuroscience.

[18]  D. Copenhagen,et al.  Visual Stimulation Is Required for Refinement of ON and OFF Pathways in Postnatal Retina , 2003, Neuron.

[19]  E. S. Ruthazer,et al.  Activity-Dependent Transcription of BDNF Enhances Visual Acuity during Development , 2011, Neuron.

[20]  M. Sur,et al.  Pattern formation by retinal afferents in the ferret lateral geniculate nucleus: Developmental segregation and the role of N‐methyl‐D‐aspartate receptors , 1999, The Journal of comparative neurology.

[21]  John G Flanagan,et al.  Ephrin-As and neural activity are required for eye-specific patterning during retinogeniculate mapping , 2005, Nature Neuroscience.

[22]  Bryan M. Hooks,et al.  Distinct Roles for Spontaneous and Visual Activity in Remodeling of the Retinogeniculate Synapse , 2006, Neuron.

[23]  W. Regehr,et al.  Developmental Remodeling of the Retinogeniculate Synapse , 2000, Neuron.

[24]  Michael C. Crair,et al.  Visual Circuit Development Requires Patterned Activity Mediated by Retinal Acetylcholine Receptors , 2014, Neuron.

[25]  C. Enroth-Cugell,et al.  The contrast sensitivity of retinal ganglion cells of the cat , 1966, The Journal of physiology.

[26]  B. Chapman,et al.  Epibatidine Blocks Eye-Specific Segregation in Ferret Dorsal Lateral Geniculate Nucleus during Stage III Retinal Waves , 2015, PloS one.

[27]  S M Archer,et al.  Abnormal development of kitten retino-geniculate connectivity in the absence of action potentials. , 1982, Science.

[28]  Chinfei Chen,et al.  Changes in input strength and number are driven by distinct mechanisms at the retinogeniculate synapse. , 2014, Journal of neurophysiology.

[29]  C. Shatz,et al.  An Instructive Role for Retinal Waves in the Development of Retinogeniculate Connectivity , 2002, Neuron.

[30]  R. C. Rentería,et al.  Receptive field center size decreases and firing properties mature in ON and OFF retinal ganglion cells after eye opening in the mouse. , 2011, Journal of neurophysiology.

[31]  B. Chapman,et al.  Cortical Cell Orientation Selectivity Fails to Develop in the Absence of ON-Center Retinal Ganglion Cell Activity , 2000, The Journal of Neuroscience.

[32]  Andrew D Huberman,et al.  Dynamics of Spontaneous Activity in the Fetal Macaque Retina during Development of Retinogeniculate Pathways , 2006, The Journal of Neuroscience.

[33]  C. Shatz,et al.  A Burst-Based “Hebbian” Learning Rule at Retinogeniculate Synapses Links Retinal Waves to Activity-Dependent Refinement , 2007, PLoS biology.

[34]  Jie Jia,et al.  Enriched environment induces angiogenesis and improves neural function outcomes in rat stroke model , 2014, Journal of the Neurological Sciences.

[35]  G. Awatramani,et al.  Origin of Transient and Sustained Responses in Ganglion Cells of the Retina , 2000, The Journal of Neuroscience.

[36]  R. Shapley,et al.  The use of m-sequences in the analysis of visual neurons: Linear receptive field properties , 1997, Visual Neuroscience.

[37]  M. Stryker,et al.  Binocular impulse blockade prevents the formation of ocular dominance columns in cat visual cortex , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[38]  M P Stryker,et al.  The projection of the visual field onto the lateral geniculate nucleus of the ferret , 1985, The Journal of comparative neurology.

[39]  Alexander Sher,et al.  Spatial-Temporal Patterns of Retinal Waves Underlying Activity-Dependent Refinement of Retinofugal Projections , 2009, Neuron.

[40]  M. Feller,et al.  Mechanisms underlying spontaneous patterned activity in developing neural circuits , 2010, Nature Reviews Neuroscience.

[41]  Andrew D Huberman,et al.  Decoupling Eye-Specific Segregation from Lamination in the Lateral Geniculate Nucleus , 2002, The Journal of Neuroscience.

[42]  Shy Shoham,et al.  Robust, automatic spike sorting using mixtures of multivariate t-distributions , 2003, Journal of Neuroscience Methods.

[43]  Marla B. Feller,et al.  Spontaneous patterned retinal activity and the refinement of retinal projections , 2005, Progress in Neurobiology.

[44]  A. Huberman,et al.  Spontaneous Retinal Activity Mediates Development of Ocular Dominance Columns and Binocular Receptive Fields in V1 , 2006, Neuron.

[45]  R. Wong,et al.  Neurotransmission selectively regulates synapse formation in parallel circuits in vivo , 2009, Nature.

[46]  A. Huberman,et al.  The Developmental Remodeling of Eye‐Specific Afferents in the Ferret Dorsal Lateral Geniculate Nucleus , 2010, Anatomical record.

[47]  Stephen J Eglen,et al.  Detecting Pairwise Correlations in Spike Trains: An Objective Comparison of Methods and Application to the Study of Retinal Waves , 2014, The Journal of Neuroscience.

[48]  M. Crair,et al.  Competition driven by retinal waves promotes morphological and functional synaptic development of neurons in the superior colliculus. , 2013, Journal of neurophysiology.

[49]  A. Beaudet,et al.  Mice Lacking Specific Nicotinic Acetylcholine Receptor Subunits Exhibit Dramatically Altered Spontaneous Activity Patterns and Reveal a Limited Role for Retinal Waves in Forming ON and OFF Circuits in the Inner Retina , 2000, The Journal of Neuroscience.

[50]  D. Baylor,et al.  Synchronous bursts of action potentials in ganglion cells of the developing mammalian retina. , 1991, Science.

[51]  C. Shatz,et al.  Transient period of correlated bursting activity during development of the mammalian retina , 1993, Neuron.