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Optimized protocol for mouse footpad immune cell isolation for single-cell RNA sequencing and flow cytometry

Single-cell RNA sequencing (scRNA-seq) requires the preparation of a highly viable single-cell suspension to get reliable sequencing results. Here, we present a protocol for isolating mouse footpad leukocytes while maintaining high viability. We describe steps for footpad collection, enzymatic tissu...

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Autores principales: Hameed, Muddassar, Rai, Pallavi, Makris, Melissa, Weger-Lucarelli, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10339044/
https://www.ncbi.nlm.nih.gov/pubmed/37402171
http://dx.doi.org/10.1016/j.xpro.2023.102409
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author Hameed, Muddassar
Rai, Pallavi
Makris, Melissa
Weger-Lucarelli, James
author_facet Hameed, Muddassar
Rai, Pallavi
Makris, Melissa
Weger-Lucarelli, James
author_sort Hameed, Muddassar
collection PubMed
description Single-cell RNA sequencing (scRNA-seq) requires the preparation of a highly viable single-cell suspension to get reliable sequencing results. Here, we present a protocol for isolating mouse footpad leukocytes while maintaining high viability. We describe steps for footpad collection, enzymatic tissue dissociation, leukocyte isolation and purification, and cell fixation and preservation. We then detail combinatorial barcoding, library preparation, scRNA-seq, and data analysis. Cells can be used to generate a complete molecular atlas at the single cell level.
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spelling pubmed-103390442023-07-14 Optimized protocol for mouse footpad immune cell isolation for single-cell RNA sequencing and flow cytometry Hameed, Muddassar Rai, Pallavi Makris, Melissa Weger-Lucarelli, James STAR Protoc Protocol Single-cell RNA sequencing (scRNA-seq) requires the preparation of a highly viable single-cell suspension to get reliable sequencing results. Here, we present a protocol for isolating mouse footpad leukocytes while maintaining high viability. We describe steps for footpad collection, enzymatic tissue dissociation, leukocyte isolation and purification, and cell fixation and preservation. We then detail combinatorial barcoding, library preparation, scRNA-seq, and data analysis. Cells can be used to generate a complete molecular atlas at the single cell level. Elsevier 2023-07-03 /pmc/articles/PMC10339044/ /pubmed/37402171 http://dx.doi.org/10.1016/j.xpro.2023.102409 Text en © 2023 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
Hameed, Muddassar
Rai, Pallavi
Makris, Melissa
Weger-Lucarelli, James
Optimized protocol for mouse footpad immune cell isolation for single-cell RNA sequencing and flow cytometry
title Optimized protocol for mouse footpad immune cell isolation for single-cell RNA sequencing and flow cytometry
title_full Optimized protocol for mouse footpad immune cell isolation for single-cell RNA sequencing and flow cytometry
title_fullStr Optimized protocol for mouse footpad immune cell isolation for single-cell RNA sequencing and flow cytometry
title_full_unstemmed Optimized protocol for mouse footpad immune cell isolation for single-cell RNA sequencing and flow cytometry
title_short Optimized protocol for mouse footpad immune cell isolation for single-cell RNA sequencing and flow cytometry
title_sort optimized protocol for mouse footpad immune cell isolation for single-cell rna sequencing and flow cytometry
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10339044/
https://www.ncbi.nlm.nih.gov/pubmed/37402171
http://dx.doi.org/10.1016/j.xpro.2023.102409
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