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Collection of cells for single-cell RNA sequencing using high-resolution fluorescence microscopy

FACS sorting followed by single-cell RNA-sequencing (SORT-Seq) is a popular procedure to select cells of interest for single-cell transcriptomics. However, FACS is not suitable for measurement of subcellular distribution of fluorescence or for small samples (<1,000 cells). The VYCAP puncher syste...

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Detalles Bibliográficos
Autores principales: Segeren, Hendrika A., Andree, Kiki C., Oomens, Lisa, Westendorp, Bart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8353340/
https://www.ncbi.nlm.nih.gov/pubmed/34401784
http://dx.doi.org/10.1016/j.xpro.2021.100718
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author Segeren, Hendrika A.
Andree, Kiki C.
Oomens, Lisa
Westendorp, Bart
author_facet Segeren, Hendrika A.
Andree, Kiki C.
Oomens, Lisa
Westendorp, Bart
author_sort Segeren, Hendrika A.
collection PubMed
description FACS sorting followed by single-cell RNA-sequencing (SORT-Seq) is a popular procedure to select cells of interest for single-cell transcriptomics. However, FACS is not suitable for measurement of subcellular distribution of fluorescence or for small samples (<1,000 cells). The VYCAP puncher system overcomes these limitations. Here, we describe a workflow to capture, image, and collect fluorescent human retina pigment epithelium cells for SORT-Seq using this system. The workflow can be used for any cell type with a diameter of ∼5–50 μm. For complete details on the use and execution of this protocol, please refer to Segeren et al. (2020).
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spelling pubmed-83533402021-08-15 Collection of cells for single-cell RNA sequencing using high-resolution fluorescence microscopy Segeren, Hendrika A. Andree, Kiki C. Oomens, Lisa Westendorp, Bart STAR Protoc Protocol FACS sorting followed by single-cell RNA-sequencing (SORT-Seq) is a popular procedure to select cells of interest for single-cell transcriptomics. However, FACS is not suitable for measurement of subcellular distribution of fluorescence or for small samples (<1,000 cells). The VYCAP puncher system overcomes these limitations. Here, we describe a workflow to capture, image, and collect fluorescent human retina pigment epithelium cells for SORT-Seq using this system. The workflow can be used for any cell type with a diameter of ∼5–50 μm. For complete details on the use and execution of this protocol, please refer to Segeren et al. (2020). Elsevier 2021-08-05 /pmc/articles/PMC8353340/ /pubmed/34401784 http://dx.doi.org/10.1016/j.xpro.2021.100718 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Segeren, Hendrika A.
Andree, Kiki C.
Oomens, Lisa
Westendorp, Bart
Collection of cells for single-cell RNA sequencing using high-resolution fluorescence microscopy
title Collection of cells for single-cell RNA sequencing using high-resolution fluorescence microscopy
title_full Collection of cells for single-cell RNA sequencing using high-resolution fluorescence microscopy
title_fullStr Collection of cells for single-cell RNA sequencing using high-resolution fluorescence microscopy
title_full_unstemmed Collection of cells for single-cell RNA sequencing using high-resolution fluorescence microscopy
title_short Collection of cells for single-cell RNA sequencing using high-resolution fluorescence microscopy
title_sort collection of cells for single-cell rna sequencing using high-resolution fluorescence microscopy
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8353340/
https://www.ncbi.nlm.nih.gov/pubmed/34401784
http://dx.doi.org/10.1016/j.xpro.2021.100718
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