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High-Throughput Single-Cell Manipulation in Brain Tissue
The complexity of neurons and neuronal circuits in brain tissue requires the genetic manipulation, labeling, and tracking of single cells. However, current methods for manipulating cells in brain tissue are limited to either bulk techniques, lacking single-cell accuracy, or manual methods that provi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334978/ https://www.ncbi.nlm.nih.gov/pubmed/22536416 http://dx.doi.org/10.1371/journal.pone.0035603 |
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author | Steinmeyer, Joseph D. Yanik, Mehmet Fatih |
author_facet | Steinmeyer, Joseph D. Yanik, Mehmet Fatih |
author_sort | Steinmeyer, Joseph D. |
collection | PubMed |
description | The complexity of neurons and neuronal circuits in brain tissue requires the genetic manipulation, labeling, and tracking of single cells. However, current methods for manipulating cells in brain tissue are limited to either bulk techniques, lacking single-cell accuracy, or manual methods that provide single-cell accuracy but at significantly lower throughputs and repeatability. Here, we demonstrate high-throughput, efficient, reliable, and combinatorial delivery of multiple genetic vectors and reagents into targeted cells within the same tissue sample with single-cell accuracy. Our system automatically loads nanoliter-scale volumes of reagents into a micropipette from multiwell plates, targets and transfects single cells in brain tissues using a robust electroporation technique, and finally preps the micropipette by automated cleaning for repeating the transfection cycle. We demonstrate multi-colored labeling of adjacent cells, both in organotypic and acute slices, and transfection of plasmids encoding different protein isoforms into neurons within the same brain tissue for analysis of their effects on linear dendritic spine density. Our platform could also be used to rapidly deliver, both ex vivo and in vivo, a variety of genetic vectors, including optogenetic and cell-type specific agents, as well as fast-acting reagents such as labeling dyes, calcium sensors, and voltage sensors to manipulate and track neuronal circuit activity at single-cell resolution. |
format | Online Article Text |
id | pubmed-3334978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33349782012-04-25 High-Throughput Single-Cell Manipulation in Brain Tissue Steinmeyer, Joseph D. Yanik, Mehmet Fatih PLoS One Research Article The complexity of neurons and neuronal circuits in brain tissue requires the genetic manipulation, labeling, and tracking of single cells. However, current methods for manipulating cells in brain tissue are limited to either bulk techniques, lacking single-cell accuracy, or manual methods that provide single-cell accuracy but at significantly lower throughputs and repeatability. Here, we demonstrate high-throughput, efficient, reliable, and combinatorial delivery of multiple genetic vectors and reagents into targeted cells within the same tissue sample with single-cell accuracy. Our system automatically loads nanoliter-scale volumes of reagents into a micropipette from multiwell plates, targets and transfects single cells in brain tissues using a robust electroporation technique, and finally preps the micropipette by automated cleaning for repeating the transfection cycle. We demonstrate multi-colored labeling of adjacent cells, both in organotypic and acute slices, and transfection of plasmids encoding different protein isoforms into neurons within the same brain tissue for analysis of their effects on linear dendritic spine density. Our platform could also be used to rapidly deliver, both ex vivo and in vivo, a variety of genetic vectors, including optogenetic and cell-type specific agents, as well as fast-acting reagents such as labeling dyes, calcium sensors, and voltage sensors to manipulate and track neuronal circuit activity at single-cell resolution. Public Library of Science 2012-04-20 /pmc/articles/PMC3334978/ /pubmed/22536416 http://dx.doi.org/10.1371/journal.pone.0035603 Text en Steinmeyer, Yanik. 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 Steinmeyer, Joseph D. Yanik, Mehmet Fatih High-Throughput Single-Cell Manipulation in Brain Tissue |
title | High-Throughput Single-Cell Manipulation in Brain Tissue |
title_full | High-Throughput Single-Cell Manipulation in Brain Tissue |
title_fullStr | High-Throughput Single-Cell Manipulation in Brain Tissue |
title_full_unstemmed | High-Throughput Single-Cell Manipulation in Brain Tissue |
title_short | High-Throughput Single-Cell Manipulation in Brain Tissue |
title_sort | high-throughput single-cell manipulation in brain tissue |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334978/ https://www.ncbi.nlm.nih.gov/pubmed/22536416 http://dx.doi.org/10.1371/journal.pone.0035603 |
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