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Conventional NK cells and ILC1 are partially ablated in the livers of Ncr1 (iCre)Tbx21 (fl/fl) mice
Mouse liver contains both Eomes-dependent conventional natural killer (cNK) cells and Tbet-dependent liver-resident type I innate lymphoid cells (ILC1). In order to better understand the role of ILC1, we attempted to generate mice that would lack liver ILC1, while retaining cNK, by conditional delet...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543419/ https://www.ncbi.nlm.nih.gov/pubmed/28815219 http://dx.doi.org/10.12688/wellcomeopenres.11741.2 |
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author | Cuff, Antonia O. Male, Victoria |
author_facet | Cuff, Antonia O. Male, Victoria |
author_sort | Cuff, Antonia O. |
collection | PubMed |
description | Mouse liver contains both Eomes-dependent conventional natural killer (cNK) cells and Tbet-dependent liver-resident type I innate lymphoid cells (ILC1). In order to better understand the role of ILC1, we attempted to generate mice that would lack liver ILC1, while retaining cNK, by conditional deletion of Tbet in NKp46+ cells. Here we report that the Ncr1 (iCre)Tbx21 (fl/fl) mouse has a roughly equivalent reduction in both the cNK and ILC1 compartments of the liver, limiting its utility for investigating the relative contributions of these two cell types in disease models. We also describe the phenotype of these mice with respect to NK cells, ILC1 and NKp46 (+) ILC3 in the spleen and small intestine lamina propria. |
format | Online Article Text |
id | pubmed-5543419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-55434192017-08-16 Conventional NK cells and ILC1 are partially ablated in the livers of Ncr1 (iCre)Tbx21 (fl/fl) mice Cuff, Antonia O. Male, Victoria Wellcome Open Res Research Note Mouse liver contains both Eomes-dependent conventional natural killer (cNK) cells and Tbet-dependent liver-resident type I innate lymphoid cells (ILC1). In order to better understand the role of ILC1, we attempted to generate mice that would lack liver ILC1, while retaining cNK, by conditional deletion of Tbet in NKp46+ cells. Here we report that the Ncr1 (iCre)Tbx21 (fl/fl) mouse has a roughly equivalent reduction in both the cNK and ILC1 compartments of the liver, limiting its utility for investigating the relative contributions of these two cell types in disease models. We also describe the phenotype of these mice with respect to NK cells, ILC1 and NKp46 (+) ILC3 in the spleen and small intestine lamina propria. F1000Research 2017-07-05 /pmc/articles/PMC5543419/ /pubmed/28815219 http://dx.doi.org/10.12688/wellcomeopenres.11741.2 Text en Copyright: © 2017 Cuff AO and Male V http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Note Cuff, Antonia O. Male, Victoria Conventional NK cells and ILC1 are partially ablated in the livers of Ncr1 (iCre)Tbx21 (fl/fl) mice |
title | Conventional NK cells and ILC1 are partially ablated in the livers of Ncr1
(iCre)Tbx21
(fl/fl) mice |
title_full | Conventional NK cells and ILC1 are partially ablated in the livers of Ncr1
(iCre)Tbx21
(fl/fl) mice |
title_fullStr | Conventional NK cells and ILC1 are partially ablated in the livers of Ncr1
(iCre)Tbx21
(fl/fl) mice |
title_full_unstemmed | Conventional NK cells and ILC1 are partially ablated in the livers of Ncr1
(iCre)Tbx21
(fl/fl) mice |
title_short | Conventional NK cells and ILC1 are partially ablated in the livers of Ncr1
(iCre)Tbx21
(fl/fl) mice |
title_sort | conventional nk cells and ilc1 are partially ablated in the livers of ncr1
(icre)tbx21
(fl/fl) mice |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543419/ https://www.ncbi.nlm.nih.gov/pubmed/28815219 http://dx.doi.org/10.12688/wellcomeopenres.11741.2 |
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