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Simultaneous two-photon activation of presynaptic cells and calcium imaging in postsynaptic dendritic spines
BACKGROUND: Dendritic spines of pyramidal neurons are distributed along the complicated structure of the dendritic branches and possess a variety of morphologies associated with synaptic strength. The location and structure of dendritic spines determine the extent of synaptic input integration in th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269225/ https://www.ncbi.nlm.nih.gov/pubmed/22330013 http://dx.doi.org/10.1186/2042-1001-1-2 |
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author | Matsuzaki, Masanori Ellis-Davies, Graham CR Kanemoto, Yuya Kasai, Haruo |
author_facet | Matsuzaki, Masanori Ellis-Davies, Graham CR Kanemoto, Yuya Kasai, Haruo |
author_sort | Matsuzaki, Masanori |
collection | PubMed |
description | BACKGROUND: Dendritic spines of pyramidal neurons are distributed along the complicated structure of the dendritic branches and possess a variety of morphologies associated with synaptic strength. The location and structure of dendritic spines determine the extent of synaptic input integration in the postsynaptic neuron. However, how spine location or size relates to the position of innervating presynaptic cells is not yet known. This report describes a new method that represents a first step toward addressing this issue. RESULTS: The technique combines two-photon uncaging of glutamate over a broad area (~500 × 250 × 100 μm) with two-photon calcium imaging in a narrow region (~50 × 10 × 1 μm). The former was used for systematic activation of layer 2/3 pyramidal cells in the rat motor cortex, while the latter was used to detect the dendritic spines of layer 5 pyramidal cells that were innervated by some of the photoactivated cells. This technique allowed identification of various sizes of innervated spine located <140 μm laterally from the postsynaptic soma. Spines distal to their parent soma were preferentially innervated by cells on the ipsilateral side. No cluster of neurons innervating the same dendritic branch was detected. CONCLUSIONS: This new method will be a powerful tool for clarifying the microarchitecture of synaptic connections, including the positional and structural characteristics of dendritic spines along the dendrites. |
format | Online Article Text |
id | pubmed-3269225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32692252012-02-01 Simultaneous two-photon activation of presynaptic cells and calcium imaging in postsynaptic dendritic spines Matsuzaki, Masanori Ellis-Davies, Graham CR Kanemoto, Yuya Kasai, Haruo Neural Syst Circuits Research BACKGROUND: Dendritic spines of pyramidal neurons are distributed along the complicated structure of the dendritic branches and possess a variety of morphologies associated with synaptic strength. The location and structure of dendritic spines determine the extent of synaptic input integration in the postsynaptic neuron. However, how spine location or size relates to the position of innervating presynaptic cells is not yet known. This report describes a new method that represents a first step toward addressing this issue. RESULTS: The technique combines two-photon uncaging of glutamate over a broad area (~500 × 250 × 100 μm) with two-photon calcium imaging in a narrow region (~50 × 10 × 1 μm). The former was used for systematic activation of layer 2/3 pyramidal cells in the rat motor cortex, while the latter was used to detect the dendritic spines of layer 5 pyramidal cells that were innervated by some of the photoactivated cells. This technique allowed identification of various sizes of innervated spine located <140 μm laterally from the postsynaptic soma. Spines distal to their parent soma were preferentially innervated by cells on the ipsilateral side. No cluster of neurons innervating the same dendritic branch was detected. CONCLUSIONS: This new method will be a powerful tool for clarifying the microarchitecture of synaptic connections, including the positional and structural characteristics of dendritic spines along the dendrites. BioMed Central 2011-01-26 /pmc/articles/PMC3269225/ /pubmed/22330013 http://dx.doi.org/10.1186/2042-1001-1-2 Text en Copyright ©2011 Matsuzaki et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Matsuzaki, Masanori Ellis-Davies, Graham CR Kanemoto, Yuya Kasai, Haruo Simultaneous two-photon activation of presynaptic cells and calcium imaging in postsynaptic dendritic spines |
title | Simultaneous two-photon activation of presynaptic cells and calcium imaging in postsynaptic dendritic spines |
title_full | Simultaneous two-photon activation of presynaptic cells and calcium imaging in postsynaptic dendritic spines |
title_fullStr | Simultaneous two-photon activation of presynaptic cells and calcium imaging in postsynaptic dendritic spines |
title_full_unstemmed | Simultaneous two-photon activation of presynaptic cells and calcium imaging in postsynaptic dendritic spines |
title_short | Simultaneous two-photon activation of presynaptic cells and calcium imaging in postsynaptic dendritic spines |
title_sort | simultaneous two-photon activation of presynaptic cells and calcium imaging in postsynaptic dendritic spines |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269225/ https://www.ncbi.nlm.nih.gov/pubmed/22330013 http://dx.doi.org/10.1186/2042-1001-1-2 |
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