Developmental patterning of glutamatergic synapses onto retinal ganglion cells

<p>Abstract</p> <p>Background</p> <p>Neurons receive excitatory synaptic inputs that are distributed across their dendritic arbors at densities and with spatial patterns that influence their output. How specific synaptic distributions are attained during development is...

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Main Authors: Schubert Timm, Morgan Josh L, Wong Rachel OL
Format: Article
Language:English
Published: BMC 2008-03-01
Series:Neural Development
Online Access:http://www.neuraldevelopment.com/content/3/1/8
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author Schubert Timm
Morgan Josh L
Wong Rachel OL
author_facet Schubert Timm
Morgan Josh L
Wong Rachel OL
author_sort Schubert Timm
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Neurons receive excitatory synaptic inputs that are distributed across their dendritic arbors at densities and with spatial patterns that influence their output. How specific synaptic distributions are attained during development is not well understood. The distribution of glutamatergic inputs across the dendritic arbors of mammalian retinal ganglion cells (RGCs) has long been correlated to the spatial receptive field profiles of these neurons. Thus, determining how glutamatergic inputs are patterned onto RGC dendritic arbors during development could provide insight into the cellular mechanisms that shape their functional receptive fields.</p> <p>Results</p> <p>We transfected developing and mature mouse RGCs with plasmids encoding fluorescent proteins that label their dendrites and glutamatergic postsynaptic sites. We found that as dendritic density (dendritic length per unit area of dendritic field) decreases with maturation, the density of synapses along the dendrites increases. These changes appear coordinated such that RGCs attain the mature average density of postsynaptic sites per unit area (areal density) by the time synaptic function emerges. Furthermore, stereotypic centro-peripheral gradients in the areal density of synapses across the arbor of RGCs are established at an early developmental stage.</p> <p>Conclusion</p> <p>The spatial pattern of glutamatergic inputs onto RGCs arises early in synaptogenesis despite ensuing reorganization of dendritic structure. We raise the possibility that these early patterns of synaptic distributions may arise from constraints placed on the number of contacts presynaptic neurons are able to make with the RGCs.</p>
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spelling doaj.art-160eab433074443d9ca72dcf7a5ecf342022-12-22T00:56:07ZengBMCNeural Development1749-81042008-03-0131810.1186/1749-8104-3-8Developmental patterning of glutamatergic synapses onto retinal ganglion cellsSchubert TimmMorgan Josh LWong Rachel OL<p>Abstract</p> <p>Background</p> <p>Neurons receive excitatory synaptic inputs that are distributed across their dendritic arbors at densities and with spatial patterns that influence their output. How specific synaptic distributions are attained during development is not well understood. The distribution of glutamatergic inputs across the dendritic arbors of mammalian retinal ganglion cells (RGCs) has long been correlated to the spatial receptive field profiles of these neurons. Thus, determining how glutamatergic inputs are patterned onto RGC dendritic arbors during development could provide insight into the cellular mechanisms that shape their functional receptive fields.</p> <p>Results</p> <p>We transfected developing and mature mouse RGCs with plasmids encoding fluorescent proteins that label their dendrites and glutamatergic postsynaptic sites. We found that as dendritic density (dendritic length per unit area of dendritic field) decreases with maturation, the density of synapses along the dendrites increases. These changes appear coordinated such that RGCs attain the mature average density of postsynaptic sites per unit area (areal density) by the time synaptic function emerges. Furthermore, stereotypic centro-peripheral gradients in the areal density of synapses across the arbor of RGCs are established at an early developmental stage.</p> <p>Conclusion</p> <p>The spatial pattern of glutamatergic inputs onto RGCs arises early in synaptogenesis despite ensuing reorganization of dendritic structure. We raise the possibility that these early patterns of synaptic distributions may arise from constraints placed on the number of contacts presynaptic neurons are able to make with the RGCs.</p>http://www.neuraldevelopment.com/content/3/1/8
spellingShingle Schubert Timm
Morgan Josh L
Wong Rachel OL
Developmental patterning of glutamatergic synapses onto retinal ganglion cells
Neural Development
title Developmental patterning of glutamatergic synapses onto retinal ganglion cells
title_full Developmental patterning of glutamatergic synapses onto retinal ganglion cells
title_fullStr Developmental patterning of glutamatergic synapses onto retinal ganglion cells
title_full_unstemmed Developmental patterning of glutamatergic synapses onto retinal ganglion cells
title_short Developmental patterning of glutamatergic synapses onto retinal ganglion cells
title_sort developmental patterning of glutamatergic synapses onto retinal ganglion cells
url http://www.neuraldevelopment.com/content/3/1/8
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