Retinocollicular Synapse Maturation and Plasticity Are Regulated by Correlated Retinal Waves

During development, spontaneous retinal waves are thought to provide an instructive signal for retinotopic map formation in the superior colliculus. In mice lacking the β2 subunit of nicotinic ACh receptors (β2−/−), correlated retinal waves are absent during the first postnatal week, but return during the second postnatal week. In control retinocollicular synapses, in vitro analysis reveals that AMPA/NMDA ratios and AMPA quantal amplitudes increase during the first postnatal week while the prevalence of silent synapses decreases. In age-matched β2−/− mice, however, these parameters remain unchanged through the first postnatal week in the absence of retinal waves, but quickly mature to control levels by the end of the second week, suggesting that the delayed onset of correlated waves is able to drive synapse maturation. To examine whether such a mechanistic relationship exists, we applied a “burst-based” plasticity protocol that mimics coincident activity during retinal waves. We find that this pattern of activation is indeed capable of inducing synaptic strengthening [long-term potentiation (LTP)] on average across genotypes early in the first postnatal week [postnatal day 3 (P3) to P4] and, interestingly, that the capacity for LTP at the end of the first week (P6–P7) is significantly greater in immature β2−/− synapses than in mature control synapses. Together, our results suggest that retinal waves drive retinocollicular synapse maturation through a learning rule that is physiologically relevant to natural wave statistics and that these synaptic changes may serve an instructive role during retinotopic map refinement.

[1]  Wei Lu,et al.  Eye Opening Rapidly Induces Synaptic Potentiation and Refinement , 2004, Neuron.

[2]  M. Feller,et al.  Retinogeniculate Axons Undergo Eye-Specific Segregation in the Absence of Eye-Specific Layers , 2002, The Journal of Neuroscience.

[3]  Li I. Zhang,et al.  Electrical activity and development of neural circuits , 2001, Nature Neuroscience.

[4]  G. Bi,et al.  Synaptic Modifications in Cultured Hippocampal Neurons: Dependence on Spike Timing, Synaptic Strength, and Postsynaptic Cell Type , 1998, The Journal of Neuroscience.

[5]  Y. Dan,et al.  Spike-timing-dependent synaptic plasticity depends on dendritic location , 2005, Nature.

[6]  R. Malinow,et al.  Maturation of a Central Glutamatergic Synapse , 1996, Science.

[7]  M A Xu-Friedman,et al.  Presynaptic strontium dynamics and synaptic transmission. , 1999, Biophysical journal.

[8]  M. Crair Neuronal activity during development: permissive or instructive? , 1999, Current Opinion in Neurobiology.

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

[10]  Arthur L. Beaudet,et al.  Multiorgan Autonomic Dysfunction in Mice Lacking the β2 and the β4 Subunits of Neuronal Nicotinic Acetylcholine Receptors , 1999, The Journal of Neuroscience.

[11]  S. Aamodt,et al.  Developmental Depression of Glutamate Neurotransmission by Chronic Low-Level Activation of NMDA Receptors , 2001, The Journal of Neuroscience.

[12]  Jianli Li,et al.  Stabilization of Axon Branch Dynamics by Synaptic Maturation , 2006, The Journal of Neuroscience.

[13]  Michael C Crair,et al.  Adenylyl cyclase I regulates AMPA receptor trafficking during mouse cortical 'barrel' map development , 2003, Nature Neuroscience.

[14]  H. Cline,et al.  LTP and activity-dependent synaptogenesis: the more alike they are, the more different they become , 1998, Current Opinion in Neurobiology.

[15]  T. Isa,et al.  Functionally different AMPA-type glutamate receptors in morphologically identified neurons in rat superficial superior colliculus , 2001, Neuroscience.

[16]  D. O'Leary,et al.  Retinotopic Map Refinement Requires Spontaneous Retinal Waves during a Brief Critical Period of Development , 2003, Neuron.

[17]  E. S. Ruthazer,et al.  Control of Axon Branch Dynamics by Correlated Activity in Vivo , 2003, Science.

[18]  Martin P Meyer,et al.  Evidence from In Vivo Imaging That Synaptogenesis Guides the Growth and Branching of Axonal Arbors by Two Distinct Mechanisms , 2006, The Journal of Neuroscience.

[19]  D. Butts Retinal Waves: Implications for Synaptic Learning Rules during Development , 2002, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.

[20]  M. Phillips,et al.  Long-Term Potentiation in the Juvenile Superior Colliculus Requires Simultaneous Activation of NMDA Receptors and L-type Ca2+ Channels and Reflects Addition of Newly Functional Synapses , 2006, The Journal of Neuroscience.

[21]  P. J. Sjöström,et al.  A Cooperative Switch Determines the Sign of Synaptic Plasticity in Distal Dendrites of Neocortical Pyramidal Neurons , 2006, Neuron.

[22]  C. Shatz,et al.  Synaptic Activity and the Construction of Cortical Circuits , 1996, Science.

[23]  Michael C Crair,et al.  Evidence for an Instructive Role of Retinal Activity in Retinotopic Map Refinement in the Superior Colliculus of the Mouse , 2005, The Journal of Neuroscience.

[24]  J. Isaac,et al.  Evidence for silent synapses: Implications for the expression of LTP , 1995, Neuron.

[25]  S. Rumpel,et al.  Silent Synapses in the Developing Rat Visual Cortex: Evidence for Postsynaptic Expression of Synaptic Plasticity , 1998, The Journal of Neuroscience.

[26]  Y. Okada,et al.  Ipsilateral corticotectal pathway inhibits the formation of long-term potentiation (LTP) in the rat superior colliculus through GABAergic mechanism , 1993, Brain Research.

[27]  Michael C. Crair,et al.  A critical period for long-term potentiation at thalamocortical synapses , 1995, Nature.

[28]  Michael C. Crair,et al.  Developmental Homeostasis of Mouse Retinocollicular Synapses , 2007, The Journal of Neuroscience.

[29]  P. Pavlidis,et al.  Pair Recordings Reveal All-Silent Synaptic Connections and the Postsynaptic Expression of Long-Term Potentiation , 2001, Neuron.

[30]  Michael C. Crair,et al.  Silent Synapses during Development of Thalamocortical Inputs , 1997, Neuron.

[31]  D. Feldman,et al.  Synaptic plasticity at thalamocortical synapses in developing rat somatosensory cortex: LTP, LTD, and silent synapses. , 1999, Journal of neurobiology.

[32]  R. Malinow,et al.  Activation of postsynaptically silent synapses during pairing-induced LTP in CA1 region of hippocampal slice , 1995, Nature.

[33]  M. Constantine-Paton,et al.  N-methyl-D-aspartate receptor antagonists disrupt the formation of a mammalian neural map. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[34]  K. Svoboda,et al.  Experience Strengthening Transmission by Driving AMPA Receptors into Synapses , 2003, Science.

[35]  M. Colonnese,et al.  Developmental period for N‐methyl‐D‐aspartate (NMDA) receptor‐dependent synapse elimination correlated with visuotopic map refinement , 2006, The Journal of comparative neurology.

[36]  Tohru Yoshioka,et al.  GABAB receptor activation enhances mGluR-mediated responses at cerebellar excitatory synapses , 2001, Nature Neuroscience.

[37]  L. Trussell,et al.  Cell-specific, spike timing–dependent plasticities in the dorsal cochlear nucleus , 2004, Nature Neuroscience.

[38]  Y. Okada,et al.  NMDA receptor, protein kinase C and calmodulin system participate in the long-term potentiation in guinea pig superior colliculus slices , 1993, Brain Research.

[39]  Mark F. Bear,et al.  Co-regulation of long-term potentiation and experience-dependent synaptic plasticity in visual cortex by age and experience , 1995, Nature.

[40]  Marla B Feller,et al.  High frequency, synchronized bursting drives eye-specific segregation of retinogeniculate projections , 2005, Nature Neuroscience.

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

[42]  R. Malenka,et al.  AMPA receptor trafficking and synaptic plasticity. , 2002, Annual review of neuroscience.

[43]  A. Konnerth,et al.  Long-term potentiation and functional synapse induction in developing hippocampus , 1996, Nature.

[44]  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.

[45]  Y. Dan,et al.  Spike Timing-Dependent Plasticity of Neural Circuits , 2004, Neuron.

[46]  K. Fox,et al.  Presynaptic efficacy directs normalization of synaptic strength in layer 2/3 rat neocortex after paired activity. , 2007, Journal of neurophysiology.

[47]  D. Debanne,et al.  Heterogeneity of Synaptic Plasticity at Unitary CA3–CA1 and CA3–CA3 Connections in Rat Hippocampal Slice Cultures , 1999, The Journal of Neuroscience.

[48]  F. Lo,et al.  Properties of LTD and LTP of retinocollicular synaptic transmission in the developing rat superior colliculus , 2002, The European journal of neuroscience.

[49]  M. Colonnese,et al.  Chronic NMDA receptor blockade from birth delays the maturation of NMDA currents, but does not affect AMPA/kainate currents. , 2003, Journal of neurophysiology.

[50]  Herwig Baier,et al.  Regulation of axon growth in vivo by activity-based competition , 2005, Nature.

[51]  J. Isaacson,et al.  Synapse-Specific Downregulation of NMDA Receptors by Early Experience: A Critical Period for Plasticity of Sensory Input to Olfactory Cortex , 2005, Neuron.

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

[53]  M. Bear,et al.  Experience-dependent modification of synaptic plasticity in visual cortex , 1996, Nature.

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