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Dissociation and inDrops microfluidic encapsulation of human gut tissues for single-cell atlasing studies

In droplet-based single-cell RNA-sequencing (scRNA-seq) experiments, cells, along with some of their surrounding buffer and ambient material, are encapsulated into droplets for mRNA capture and barcoding. This protocol details the steps for human gut tissue dissociation using cold active protease, a...

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Detalles Bibliográficos
Autores principales: Simmons, Alan J., Lau, Ken S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307676/
https://www.ncbi.nlm.nih.gov/pubmed/35880121
http://dx.doi.org/10.1016/j.xpro.2022.101570
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author Simmons, Alan J.
Lau, Ken S.
author_facet Simmons, Alan J.
Lau, Ken S.
author_sort Simmons, Alan J.
collection PubMed
description In droplet-based single-cell RNA-sequencing (scRNA-seq) experiments, cells, along with some of their surrounding buffer and ambient material, are encapsulated into droplets for mRNA capture and barcoding. This protocol details the steps for human gut tissue dissociation using cold active protease, and subsequent isolation of single epithelial cells, with enrichment of viability through washes. Next, the steps for encapsulation on the inDrops scRNA-seq platform are described. This procedure has been demonstrated to be applicable to polyps, cancers, and inflamed tissues. For complete details on the use and execution of this protocol, please refer to Chen et al. (2021).
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spelling pubmed-93076762022-07-24 Dissociation and inDrops microfluidic encapsulation of human gut tissues for single-cell atlasing studies Simmons, Alan J. Lau, Ken S. STAR Protoc Protocol In droplet-based single-cell RNA-sequencing (scRNA-seq) experiments, cells, along with some of their surrounding buffer and ambient material, are encapsulated into droplets for mRNA capture and barcoding. This protocol details the steps for human gut tissue dissociation using cold active protease, and subsequent isolation of single epithelial cells, with enrichment of viability through washes. Next, the steps for encapsulation on the inDrops scRNA-seq platform are described. This procedure has been demonstrated to be applicable to polyps, cancers, and inflamed tissues. For complete details on the use and execution of this protocol, please refer to Chen et al. (2021). Elsevier 2022-07-19 /pmc/articles/PMC9307676/ /pubmed/35880121 http://dx.doi.org/10.1016/j.xpro.2022.101570 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Simmons, Alan J.
Lau, Ken S.
Dissociation and inDrops microfluidic encapsulation of human gut tissues for single-cell atlasing studies
title Dissociation and inDrops microfluidic encapsulation of human gut tissues for single-cell atlasing studies
title_full Dissociation and inDrops microfluidic encapsulation of human gut tissues for single-cell atlasing studies
title_fullStr Dissociation and inDrops microfluidic encapsulation of human gut tissues for single-cell atlasing studies
title_full_unstemmed Dissociation and inDrops microfluidic encapsulation of human gut tissues for single-cell atlasing studies
title_short Dissociation and inDrops microfluidic encapsulation of human gut tissues for single-cell atlasing studies
title_sort dissociation and indrops microfluidic encapsulation of human gut tissues for single-cell atlasing studies
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307676/
https://www.ncbi.nlm.nih.gov/pubmed/35880121
http://dx.doi.org/10.1016/j.xpro.2022.101570
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