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Development and function of human innate immune cells in a humanized mouse model
Mice repopulated with human hematopoietic cells are a powerful tool for the study of human hematopoiesis and immune function in vivo. However, existing humanized mouse models are unable to support development of human innate immune cells, including myeloid cells and NK cells. Here we describe a mous...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017589/ https://www.ncbi.nlm.nih.gov/pubmed/24633240 http://dx.doi.org/10.1038/nbt.2858 |
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author | Rongvaux, Anthony Willinger, Tim Martinek, Jan Strowig, Till Gearty, Sofia V. Teichmann, Lino L. Saito, Yasuyuki Marches, Florentina Halene, Stephanie Palucka, A. Karolina Manz, Markus G. Flavell, Richard A. |
author_facet | Rongvaux, Anthony Willinger, Tim Martinek, Jan Strowig, Till Gearty, Sofia V. Teichmann, Lino L. Saito, Yasuyuki Marches, Florentina Halene, Stephanie Palucka, A. Karolina Manz, Markus G. Flavell, Richard A. |
author_sort | Rongvaux, Anthony |
collection | PubMed |
description | Mice repopulated with human hematopoietic cells are a powerful tool for the study of human hematopoiesis and immune function in vivo. However, existing humanized mouse models are unable to support development of human innate immune cells, including myeloid cells and NK cells. Here we describe a mouse strain, called MI(S)TRG, in which human versions of four genes encoding cytokines important for innate immune cell development are knocked in to their respective mouse loci. The human cytokines support the development and function of monocytes/macrophages and natural killer cells derived from human fetal liver or adult CD34(+) progenitor cells injected into the mice. Human macrophages infiltrated a human tumor xenograft in MI(S)TRG mice in a manner resembling that observed in tumors obtained from human patients. This humanized mouse model may be used to model the human immune system in scenarios of health and pathology, and may enable evaluation of therapeutic candidates in an in vivo setting relevant to human physiology. |
format | Online Article Text |
id | pubmed-4017589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
record_format | MEDLINE/PubMed |
spelling | pubmed-40175892014-10-01 Development and function of human innate immune cells in a humanized mouse model Rongvaux, Anthony Willinger, Tim Martinek, Jan Strowig, Till Gearty, Sofia V. Teichmann, Lino L. Saito, Yasuyuki Marches, Florentina Halene, Stephanie Palucka, A. Karolina Manz, Markus G. Flavell, Richard A. Nat Biotechnol Article Mice repopulated with human hematopoietic cells are a powerful tool for the study of human hematopoiesis and immune function in vivo. However, existing humanized mouse models are unable to support development of human innate immune cells, including myeloid cells and NK cells. Here we describe a mouse strain, called MI(S)TRG, in which human versions of four genes encoding cytokines important for innate immune cell development are knocked in to their respective mouse loci. The human cytokines support the development and function of monocytes/macrophages and natural killer cells derived from human fetal liver or adult CD34(+) progenitor cells injected into the mice. Human macrophages infiltrated a human tumor xenograft in MI(S)TRG mice in a manner resembling that observed in tumors obtained from human patients. This humanized mouse model may be used to model the human immune system in scenarios of health and pathology, and may enable evaluation of therapeutic candidates in an in vivo setting relevant to human physiology. 2014-03-16 2014-04 /pmc/articles/PMC4017589/ /pubmed/24633240 http://dx.doi.org/10.1038/nbt.2858 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Rongvaux, Anthony Willinger, Tim Martinek, Jan Strowig, Till Gearty, Sofia V. Teichmann, Lino L. Saito, Yasuyuki Marches, Florentina Halene, Stephanie Palucka, A. Karolina Manz, Markus G. Flavell, Richard A. Development and function of human innate immune cells in a humanized mouse model |
title | Development and function of human innate immune cells in a humanized mouse model |
title_full | Development and function of human innate immune cells in a humanized mouse model |
title_fullStr | Development and function of human innate immune cells in a humanized mouse model |
title_full_unstemmed | Development and function of human innate immune cells in a humanized mouse model |
title_short | Development and function of human innate immune cells in a humanized mouse model |
title_sort | development and function of human innate immune cells in a humanized mouse model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017589/ https://www.ncbi.nlm.nih.gov/pubmed/24633240 http://dx.doi.org/10.1038/nbt.2858 |
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