Cargando…
Spatial Relationships between GABAergic and Glutamatergic Synapses on the Dendrites of Distinct Types of Mouse Retinal Ganglion Cells across Development
Neuronal output requires a concerted balance between excitatory and inhibitory (I/E) input. Like other circuits, inhibitory synaptogenesis in the retina precedes excitatory synaptogenesis. How then do neurons attain their mature balance of I/E ratios despite temporal offset in synaptogenesis? To dir...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724919/ https://www.ncbi.nlm.nih.gov/pubmed/23922756 http://dx.doi.org/10.1371/journal.pone.0069612 |
_version_ | 1782476750902525952 |
---|---|
author | Bleckert, Adam Parker, Edward D. Kang, YunHee Pancaroglu, Raika Soto, Florentina Lewis, Renate Craig, Ann Marie Wong, Rachel O. L. |
author_facet | Bleckert, Adam Parker, Edward D. Kang, YunHee Pancaroglu, Raika Soto, Florentina Lewis, Renate Craig, Ann Marie Wong, Rachel O. L. |
author_sort | Bleckert, Adam |
collection | PubMed |
description | Neuronal output requires a concerted balance between excitatory and inhibitory (I/E) input. Like other circuits, inhibitory synaptogenesis in the retina precedes excitatory synaptogenesis. How then do neurons attain their mature balance of I/E ratios despite temporal offset in synaptogenesis? To directly compare the development of glutamatergic and GABAergic synapses onto the same cell, we biolistically transfected retinal ganglion cells (RGCs) with PSD95CFP, a marker of glutamatergic postsynaptic sites, in transgenic Thy1YFPγ2 mice in which GABA(A) receptors are fluorescently tagged. We mapped YFPγ2 and PSD95CFP puncta distributions on three RGC types at postnatal day P12, shortly before eye opening, and at P21 when robust light responses in RGCs are present. The mature I(GABA)/E ratios varied among ON-Sustained (S) A-type, OFF-S A-type, and bistratified direction selective (DS) RGCs. These ratios were attained at different rates, before eye-opening for ON-S and OFF-S A-type, and after eye-opening for DS RGCs. At both ages examined, the I(GABA)/E ratio was uniform across the arbors of the three RGC types. Furthermore, measurements of the distances between neighboring PSD95CFP and YFPγ2 puncta on RGC dendrites indicate that their local relationship is established early in development, and cannot be predicted by random organization. These close spatial associations between glutamatergic and GABAergic postsynaptic sites appear to represent local synaptic arrangements revealed by correlative light and EM reconstructions of a single RGC's dendrites. Thus, although RGC types have different I(GABA)/E ratios and establish these ratios at separate rates, the local relationship between excitatory and inhibitory inputs appear similarly constrained across the RGC types studied. |
format | Online Article Text |
id | pubmed-3724919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37249192013-08-06 Spatial Relationships between GABAergic and Glutamatergic Synapses on the Dendrites of Distinct Types of Mouse Retinal Ganglion Cells across Development Bleckert, Adam Parker, Edward D. Kang, YunHee Pancaroglu, Raika Soto, Florentina Lewis, Renate Craig, Ann Marie Wong, Rachel O. L. PLoS One Research Article Neuronal output requires a concerted balance between excitatory and inhibitory (I/E) input. Like other circuits, inhibitory synaptogenesis in the retina precedes excitatory synaptogenesis. How then do neurons attain their mature balance of I/E ratios despite temporal offset in synaptogenesis? To directly compare the development of glutamatergic and GABAergic synapses onto the same cell, we biolistically transfected retinal ganglion cells (RGCs) with PSD95CFP, a marker of glutamatergic postsynaptic sites, in transgenic Thy1YFPγ2 mice in which GABA(A) receptors are fluorescently tagged. We mapped YFPγ2 and PSD95CFP puncta distributions on three RGC types at postnatal day P12, shortly before eye opening, and at P21 when robust light responses in RGCs are present. The mature I(GABA)/E ratios varied among ON-Sustained (S) A-type, OFF-S A-type, and bistratified direction selective (DS) RGCs. These ratios were attained at different rates, before eye-opening for ON-S and OFF-S A-type, and after eye-opening for DS RGCs. At both ages examined, the I(GABA)/E ratio was uniform across the arbors of the three RGC types. Furthermore, measurements of the distances between neighboring PSD95CFP and YFPγ2 puncta on RGC dendrites indicate that their local relationship is established early in development, and cannot be predicted by random organization. These close spatial associations between glutamatergic and GABAergic postsynaptic sites appear to represent local synaptic arrangements revealed by correlative light and EM reconstructions of a single RGC's dendrites. Thus, although RGC types have different I(GABA)/E ratios and establish these ratios at separate rates, the local relationship between excitatory and inhibitory inputs appear similarly constrained across the RGC types studied. Public Library of Science 2013-07-26 /pmc/articles/PMC3724919/ /pubmed/23922756 http://dx.doi.org/10.1371/journal.pone.0069612 Text en © 2013 Bleckert et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Bleckert, Adam Parker, Edward D. Kang, YunHee Pancaroglu, Raika Soto, Florentina Lewis, Renate Craig, Ann Marie Wong, Rachel O. L. Spatial Relationships between GABAergic and Glutamatergic Synapses on the Dendrites of Distinct Types of Mouse Retinal Ganglion Cells across Development |
title | Spatial Relationships between GABAergic and Glutamatergic Synapses on the Dendrites of Distinct Types of Mouse Retinal Ganglion Cells across Development |
title_full | Spatial Relationships between GABAergic and Glutamatergic Synapses on the Dendrites of Distinct Types of Mouse Retinal Ganglion Cells across Development |
title_fullStr | Spatial Relationships between GABAergic and Glutamatergic Synapses on the Dendrites of Distinct Types of Mouse Retinal Ganglion Cells across Development |
title_full_unstemmed | Spatial Relationships between GABAergic and Glutamatergic Synapses on the Dendrites of Distinct Types of Mouse Retinal Ganglion Cells across Development |
title_short | Spatial Relationships between GABAergic and Glutamatergic Synapses on the Dendrites of Distinct Types of Mouse Retinal Ganglion Cells across Development |
title_sort | spatial relationships between gabaergic and glutamatergic synapses on the dendrites of distinct types of mouse retinal ganglion cells across development |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724919/ https://www.ncbi.nlm.nih.gov/pubmed/23922756 http://dx.doi.org/10.1371/journal.pone.0069612 |
work_keys_str_mv | AT bleckertadam spatialrelationshipsbetweengabaergicandglutamatergicsynapsesonthedendritesofdistincttypesofmouseretinalganglioncellsacrossdevelopment AT parkeredwardd spatialrelationshipsbetweengabaergicandglutamatergicsynapsesonthedendritesofdistincttypesofmouseretinalganglioncellsacrossdevelopment AT kangyunhee spatialrelationshipsbetweengabaergicandglutamatergicsynapsesonthedendritesofdistincttypesofmouseretinalganglioncellsacrossdevelopment AT pancarogluraika spatialrelationshipsbetweengabaergicandglutamatergicsynapsesonthedendritesofdistincttypesofmouseretinalganglioncellsacrossdevelopment AT sotoflorentina spatialrelationshipsbetweengabaergicandglutamatergicsynapsesonthedendritesofdistincttypesofmouseretinalganglioncellsacrossdevelopment AT lewisrenate spatialrelationshipsbetweengabaergicandglutamatergicsynapsesonthedendritesofdistincttypesofmouseretinalganglioncellsacrossdevelopment AT craigannmarie spatialrelationshipsbetweengabaergicandglutamatergicsynapsesonthedendritesofdistincttypesofmouseretinalganglioncellsacrossdevelopment AT wongrachelol spatialrelationshipsbetweengabaergicandglutamatergicsynapsesonthedendritesofdistincttypesofmouseretinalganglioncellsacrossdevelopment |