Cargando…
An in vivo gene delivery approach for the isolation of reasonable numbers of type 2 innate lymphoid cells
Group 2 innate lymphoid cells (ILC2s) are a recently recognized subset of innate lymphocytes with crucial role in mucosal immunity and tissue homeostasis. Over the past decade, substantial advances in our understanding of ILC2 biology have established them as an essential element in innate and adapt...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509459/ https://www.ncbi.nlm.nih.gov/pubmed/33005569 http://dx.doi.org/10.1016/j.mex.2020.101054 |
_version_ | 1783585601008697344 |
---|---|
author | Frech, Michael Knipfer, Lisa Wirtz, Stefan Zaiss, Mario M. |
author_facet | Frech, Michael Knipfer, Lisa Wirtz, Stefan Zaiss, Mario M. |
author_sort | Frech, Michael |
collection | PubMed |
description | Group 2 innate lymphoid cells (ILC2s) are a recently recognized subset of innate lymphocytes with crucial role in mucosal immunity and tissue homeostasis. Over the past decade, substantial advances in our understanding of ILC2 biology have established them as an essential element in innate and adaptive immunity. However, their relatively low abundance and laborious purification from mucosal tissues make their study difficult. Moreover, due to a lack of an ILC2-specific Cre mouse-line, adoptive transfer of ILC2s into ILC-deficient hosts is inevitable. Herein we describe an in-depth protocol for the induction, isolation, and expansion of murine ILC2s. By combining an in vivo gene delivery approach to boost ILC2 numbers and a cell culture strategy to expand isolated cells, large quantities of highly pure ILC2s can be obtained. The isolated cells maintain their phenotype and can be used for subsequent cell transfer or in vitro studies. In comparison to previous protocols, this approach is cost-effective and efficient with potential yield of more than 20 million ILC2s isolated per mouse. • Group 2 innate lymphoid cells (ILC2s) are extensively studied in mouse models and humans in recent years. • Low abundance of ILC2s and current lack of specific ILC2 knockout mice makes in vivo research challenging. • This method allows high and pure ILC2 numbers for in vitro or adoptive in vivo transfer experiments. |
format | Online Article Text |
id | pubmed-7509459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-75094592020-09-30 An in vivo gene delivery approach for the isolation of reasonable numbers of type 2 innate lymphoid cells Frech, Michael Knipfer, Lisa Wirtz, Stefan Zaiss, Mario M. MethodsX Method Article Group 2 innate lymphoid cells (ILC2s) are a recently recognized subset of innate lymphocytes with crucial role in mucosal immunity and tissue homeostasis. Over the past decade, substantial advances in our understanding of ILC2 biology have established them as an essential element in innate and adaptive immunity. However, their relatively low abundance and laborious purification from mucosal tissues make their study difficult. Moreover, due to a lack of an ILC2-specific Cre mouse-line, adoptive transfer of ILC2s into ILC-deficient hosts is inevitable. Herein we describe an in-depth protocol for the induction, isolation, and expansion of murine ILC2s. By combining an in vivo gene delivery approach to boost ILC2 numbers and a cell culture strategy to expand isolated cells, large quantities of highly pure ILC2s can be obtained. The isolated cells maintain their phenotype and can be used for subsequent cell transfer or in vitro studies. In comparison to previous protocols, this approach is cost-effective and efficient with potential yield of more than 20 million ILC2s isolated per mouse. • Group 2 innate lymphoid cells (ILC2s) are extensively studied in mouse models and humans in recent years. • Low abundance of ILC2s and current lack of specific ILC2 knockout mice makes in vivo research challenging. • This method allows high and pure ILC2 numbers for in vitro or adoptive in vivo transfer experiments. Elsevier 2020-09-10 /pmc/articles/PMC7509459/ /pubmed/33005569 http://dx.doi.org/10.1016/j.mex.2020.101054 Text en © 2020 The Authors. Published by Elsevier B.V. http://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 | Method Article Frech, Michael Knipfer, Lisa Wirtz, Stefan Zaiss, Mario M. An in vivo gene delivery approach for the isolation of reasonable numbers of type 2 innate lymphoid cells |
title | An in vivo gene delivery approach for the isolation of reasonable numbers of type 2 innate lymphoid cells |
title_full | An in vivo gene delivery approach for the isolation of reasonable numbers of type 2 innate lymphoid cells |
title_fullStr | An in vivo gene delivery approach for the isolation of reasonable numbers of type 2 innate lymphoid cells |
title_full_unstemmed | An in vivo gene delivery approach for the isolation of reasonable numbers of type 2 innate lymphoid cells |
title_short | An in vivo gene delivery approach for the isolation of reasonable numbers of type 2 innate lymphoid cells |
title_sort | in vivo gene delivery approach for the isolation of reasonable numbers of type 2 innate lymphoid cells |
topic | Method Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509459/ https://www.ncbi.nlm.nih.gov/pubmed/33005569 http://dx.doi.org/10.1016/j.mex.2020.101054 |
work_keys_str_mv | AT frechmichael aninvivogenedeliveryapproachfortheisolationofreasonablenumbersoftype2innatelymphoidcells AT knipferlisa aninvivogenedeliveryapproachfortheisolationofreasonablenumbersoftype2innatelymphoidcells AT wirtzstefan aninvivogenedeliveryapproachfortheisolationofreasonablenumbersoftype2innatelymphoidcells AT zaissmariom aninvivogenedeliveryapproachfortheisolationofreasonablenumbersoftype2innatelymphoidcells AT frechmichael invivogenedeliveryapproachfortheisolationofreasonablenumbersoftype2innatelymphoidcells AT knipferlisa invivogenedeliveryapproachfortheisolationofreasonablenumbersoftype2innatelymphoidcells AT wirtzstefan invivogenedeliveryapproachfortheisolationofreasonablenumbersoftype2innatelymphoidcells AT zaissmariom invivogenedeliveryapproachfortheisolationofreasonablenumbersoftype2innatelymphoidcells |