Functional Interactions between Newborn and Mature Neurons Leading to Integration into Established Neuronal Circuits

Summary From development up to adulthood, the vertebrate brain is continuously supplied with newborn neurons that integrate into established mature circuits. However, how this process is coordinated during development remains unclear. Using two-photon imaging, GCaMP5 transgenic zebrafish larvae, and sparse electroporation in the larva’s optic tectum, we monitored spontaneous and induced activity of large neuronal populations containing newborn and functionally mature neurons. We observed that the maturation of newborn neurons is a 4-day process. Initially, newborn neurons showed undeveloped dendritic arbors, no neurotransmitter identity, and were unresponsive to visual stimulation, although they displayed spontaneous calcium transients. Later on, newborn-labeled neurons began to respond to visual stimuli but in a very variable manner. At the end of the maturation period, newborn-labeled neurons exhibited visual tuning curves (spatial receptive fields and direction selectivity) and spontaneous correlated activity with neighboring functionally mature neurons. At this developmental stage, newborn-labeled neurons presented complex dendritic arbors and neurotransmitter identity (excitatory or inhibitory). Removal of retinal inputs significantly perturbed the integration of newborn neurons into the functionally mature tectal network. Our results provide a comprehensive description of the maturation of newborn neurons during development and shed light on potential mechanisms underlying their integration into a functionally mature neuronal circuit.

[1]  Johann H. Bollmann,et al.  Classification of Object Size in Retinotectal Microcircuits , 2014, Current Biology.

[2]  A. Mizrahi,et al.  Odor Processing by Adult-Born Neurons , 2014, Neuron.

[3]  Nicholas C. Spitzer,et al.  Electrical activity in early neuronal development , 2006, Nature.

[4]  Hollis T. Cline,et al.  An Evolutionarily Conserved Mechanism for Activity-Dependent Visual Circuit Development , 2016, Front. Neural Circuits.

[5]  Olaf Sporns,et al.  Connectivity and complexity: the relationship between neuroanatomy and brain dynamics , 2000, Neural Networks.

[6]  Nikolas Nikolaou,et al.  Lamination Speeds the Functional Development of Visual Circuits , 2015, Neuron.

[7]  Johann H. Bollmann,et al.  Layer-Specific Targeting of Direction-Selective Neurons in the Zebrafish Optic Tectum , 2012, Neuron.

[8]  Herwig Baier,et al.  Visual Prey Capture in Larval Zebrafish Is Controlled by Identified Reticulospinal Neurons Downstream of the Tectum , 2005, The Journal of Neuroscience.

[9]  Rainer W. Friedrich,et al.  Circuit Neuroscience in Zebrafish , 2010, Current Biology.

[10]  Ethan K. Scott,et al.  Filtering of Visual Information in the Tectum by an Identified Neural Circuit , 2010, Science.

[11]  K. Kawakami,et al.  Stable integration and conditional expression of electroporated transgenes in chicken embryos. , 2007, Developmental biology.

[12]  Ethan K. Scott,et al.  The cellular architecture of the larval zebrafish tectum , as revealed by Gal 4 enhancer trap lines , 2022 .

[13]  J. H. Horne,et al.  The temporal resolution of in vivo electroporation in zebrafish: a method for time-resolved loss of function. , 2010, Zebrafish.

[14]  Alison S. Walker,et al.  Parametric Functional Maps of Visual Inputs to the Tectum , 2012, Neuron.

[15]  Aristides B. Arrenberg,et al.  Deep Brain Photoreceptors Control Light-Seeking Behavior in Zebrafish Larvae , 2012, Current Biology.

[16]  Chie Satou,et al.  Transgenic tools to characterize neuronal properties of discrete populations of zebrafish neurons , 2013, Development.

[17]  R. M. Gaze,et al.  The evolution of the retinotectal map during development in Xenopus , 1974, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[18]  X. Wang,et al.  Harnessing a High Cargo-Capacity Transposon for Genetic Applications in Vertebrates , 2006, PLoS genetics.

[19]  Herwig Baier,et al.  Characterization of Genetically Targeted Neuron Types in the Zebrafish Optic Tectum , 2011, Front. Neural Circuits.

[20]  Melissa Hardy,et al.  The Tol2kit: A multisite gateway‐based construction kit for Tol2 transposon transgenesis constructs , 2007, Developmental dynamics : an official publication of the American Association of Anatomists.

[21]  Atsushi Miyawaki,et al.  Illuminating cell-cycle progression in the developing zebrafish embryo , 2009, Proceedings of the National Academy of Sciences.

[22]  Ethan K. Scott,et al.  Focusing on optic tectum circuitry through the lens of genetics , 2010, BMC Biology.

[23]  Germán Sumbre,et al.  A computational toolbox and step-by-step tutorial for the analysis of neuronal population dynamics in calcium imaging data , 2017, bioRxiv.

[24]  Mark Ellisman,et al.  Synapse formation on neurons born in the adult hippocampus , 2007, Nature Neuroscience.

[25]  Wolfgang Kelsch,et al.  Genetically Increased Cell-Intrinsic Excitability Enhances Neuronal Integration into Adult Brain Circuits , 2010, Neuron.

[26]  Germán Sumbre,et al.  The Emergence of the Spatial Structure of Tectal Spontaneous Activity Is Independent of Visual Inputs , 2017, Cell reports.

[27]  Alan Carleton,et al.  Becoming a new neuron in the adult olfactory bulb , 2003, Nature Neuroscience.

[28]  A. Grinvald,et al.  Spontaneously emerging cortical representations of visual attributes , 2003, Nature.

[29]  Karel Svoboda,et al.  ScanImage: Flexible software for operating laser scanning microscopes , 2003, Biomedical engineering online.

[30]  Martin P Meyer,et al.  In vivo imaging of synapse formation on a growing dendritic arbor , 2004, Nature Neuroscience.

[31]  G. Ming,et al.  Adult Mammalian Neural Stem Cells and Neurogenesis: Five Decades Later. , 2015, Cell stem cell.

[32]  S. Romano,et al.  Sustained Rhythmic Brain Activity Underlies Visual Motion Perception in Zebrafish , 2016, Cell reports.

[33]  S. Easter,et al.  An evaluation of the hypothesis of shifting terminals in goldfish optic tectum , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[34]  M. Davidson,et al.  An Enhanced Monomeric Blue Fluorescent Protein with the High Chemical Stability of the Chromophore , 2011, PloS one.

[35]  Herwig Baier,et al.  Sensorimotor Decision Making in the Zebrafish Tectum , 2015, Current Biology.

[36]  D H Brainard,et al.  The Psychophysics Toolbox. , 1997, Spatial vision.

[37]  H. Guillou,et al.  Spatial organization of the extracellular matrix regulates cell–cell junction positioning , 2012, Proceedings of the National Academy of Sciences.

[38]  Kristen E. Severi,et al.  Control of visually guided behavior by distinct populations of spinal projection neurons , 2008, Nature Neuroscience.

[39]  C. Niell,et al.  Functional Imaging Reveals Rapid Development of Visual Response Properties in the Zebrafish Tectum , 2005, Neuron.

[40]  Maxwell H. Turner,et al.  A method for detecting molecular transport within the cerebral ventricles of live zebrafish (Danio rerio) larvae , 2012, The Journal of physiology.

[41]  J. Clarke,et al.  Focal electroporation in zebrafish embryos and larvae. , 2009, Methods in molecular biology.

[42]  Tobias Bonhoeffer,et al.  Altered Map of Visual Space in the Superior Colliculus of Mice Lacking Early Retinal Waves , 2005, The Journal of Neuroscience.

[43]  M. Hendricks,et al.  Formation of the retinotectal projection requires Esrom, an ortholog of PAM (protein associated with Myc) , 2005, Development.

[44]  Ju Young Kim,et al.  Development of hippocampal mossy fiber synaptic outputs by new neurons in the adult brain , 2008, Proceedings of the National Academy of Sciences.

[45]  R. Yuste,et al.  Visual stimuli recruit intrinsically generated cortical ensembles , 2014, Proceedings of the National Academy of Sciences.

[46]  F. Gage,et al.  Neurons born in the adult dentate gyrus form functional synapses with target cells , 2008, Nature Neuroscience.

[47]  C. Clopath,et al.  The emergence of functional microcircuits in visual cortex , 2013, Nature.

[48]  I. Foucher,et al.  Embryonic origin and lineage hierarchies of the neural progenitor subtypes building the zebrafish adult midbrain , 2016, Developmental biology.

[49]  J. Joly,et al.  Zebrafish midbrain slow-amplifying progenitors exhibit high levels of transcripts for nucleotide and ribosome biogenesis , 2013, Development.

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

[51]  H. Okamoto,et al.  Characterization of neural stem cells and their progeny in the adult zebrafish optic tectum. , 2010, Developmental biology.

[52]  Hongjun Song,et al.  GABA regulates synaptic integration of newly generated neurons in the adult brain , 2006, Nature.

[53]  Jeffrey D. Zaremba,et al.  Distinct Contribution of Adult-Born Hippocampal Granule Cells to Context Encoding , 2016, Neuron.

[54]  K. Kawakami,et al.  Left Habenula Mediates Light-Preference Behavior in Zebrafish via an Asymmetrical Visual Pathway , 2017, Neuron.

[55]  Germán Sumbre,et al.  Spontaneous Neuronal Network Dynamics Reveal Circuit’s Functional Adaptations for Behavior , 2015, Neuron.

[56]  A. F. Schinder,et al.  Unique Processing During a Period of High Excitation/Inhibition Balance in Adult-Born Neurons , 2012, Science.