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Modeling the human bone marrow niche in mice: From host bone marrow engraftment to bioengineering approaches
Xenotransplantation of patient-derived samples in mouse models has been instrumental in depicting the role of hematopoietic stem and progenitor cells in the establishment as well as progression of hematological malignancies. The foundations for this field of research have been based on the developme...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5839768/ https://www.ncbi.nlm.nih.gov/pubmed/29453226 http://dx.doi.org/10.1084/jem.20172139 |
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author | Abarrategi, Ander Mian, Syed A. Passaro, Diana Rouault-Pierre, Kevin Grey, William Bonnet, Dominique |
author_facet | Abarrategi, Ander Mian, Syed A. Passaro, Diana Rouault-Pierre, Kevin Grey, William Bonnet, Dominique |
author_sort | Abarrategi, Ander |
collection | PubMed |
description | Xenotransplantation of patient-derived samples in mouse models has been instrumental in depicting the role of hematopoietic stem and progenitor cells in the establishment as well as progression of hematological malignancies. The foundations for this field of research have been based on the development of immunodeficient mouse models, which provide normal and malignant human hematopoietic cells with a supportive microenvironment. Immunosuppressed and genetically modified mice expressing human growth factors were key milestones in patient-derived xenograft (PDX) models, highlighting the importance of developing humanized microenvironments. The latest major improvement has been the use of human bone marrow (BM) niche–forming cells to generate human–mouse chimeric BM tissues in PDXs, which can shed light on the interactions between human stroma and hematopoietic cells. Here, we summarize the methods used for human hematopoietic cell xenotransplantation and their milestones and review the latest approaches in generating humanized BM tissues in mice to study human normal and malignant hematopoiesis. |
format | Online Article Text |
id | pubmed-5839768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58397682018-09-05 Modeling the human bone marrow niche in mice: From host bone marrow engraftment to bioengineering approaches Abarrategi, Ander Mian, Syed A. Passaro, Diana Rouault-Pierre, Kevin Grey, William Bonnet, Dominique J Exp Med Reviews Xenotransplantation of patient-derived samples in mouse models has been instrumental in depicting the role of hematopoietic stem and progenitor cells in the establishment as well as progression of hematological malignancies. The foundations for this field of research have been based on the development of immunodeficient mouse models, which provide normal and malignant human hematopoietic cells with a supportive microenvironment. Immunosuppressed and genetically modified mice expressing human growth factors were key milestones in patient-derived xenograft (PDX) models, highlighting the importance of developing humanized microenvironments. The latest major improvement has been the use of human bone marrow (BM) niche–forming cells to generate human–mouse chimeric BM tissues in PDXs, which can shed light on the interactions between human stroma and hematopoietic cells. Here, we summarize the methods used for human hematopoietic cell xenotransplantation and their milestones and review the latest approaches in generating humanized BM tissues in mice to study human normal and malignant hematopoiesis. Rockefeller University Press 2018-03-05 /pmc/articles/PMC5839768/ /pubmed/29453226 http://dx.doi.org/10.1084/jem.20172139 Text en © 2018 Abarrategi et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Reviews Abarrategi, Ander Mian, Syed A. Passaro, Diana Rouault-Pierre, Kevin Grey, William Bonnet, Dominique Modeling the human bone marrow niche in mice: From host bone marrow engraftment to bioengineering approaches |
title | Modeling the human bone marrow niche in mice: From host bone marrow engraftment to bioengineering approaches |
title_full | Modeling the human bone marrow niche in mice: From host bone marrow engraftment to bioengineering approaches |
title_fullStr | Modeling the human bone marrow niche in mice: From host bone marrow engraftment to bioengineering approaches |
title_full_unstemmed | Modeling the human bone marrow niche in mice: From host bone marrow engraftment to bioengineering approaches |
title_short | Modeling the human bone marrow niche in mice: From host bone marrow engraftment to bioengineering approaches |
title_sort | modeling the human bone marrow niche in mice: from host bone marrow engraftment to bioengineering approaches |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5839768/ https://www.ncbi.nlm.nih.gov/pubmed/29453226 http://dx.doi.org/10.1084/jem.20172139 |
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