Abarrategi, A;
Mian, SA;
Passaro, D;
Rouault-Pierre, K;
Grey, W;
Bonnet, D;
(2018)
Modeling the human bone marrow niche in mice: From host bone marrow engraftment to bioengineering approaches.
Journal of Experimental Medicine
, 215
(3)
pp. 729-743.
10.1084/jem.20172139.
Preview |
Text
729.full.pdf - Published Version Download (1MB) | Preview |
Abstract
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.
Type: | Article |
---|---|
Title: | Modeling the human bone marrow niche in mice: From host bone marrow engraftment to bioengineering approaches |
Location: | United States |
Open access status: | An open access version is available from UCL Discovery |
DOI: | 10.1084/jem.20172139 |
Publisher version: | https://doi.org/10.1084/jem.20172139 |
Language: | English |
Additional information: | Copyright © 2018 Abarrategi et al. 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/). |
UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health > Genetics and Genomic Medicine Dept |
URI: | https://discovery.ucl.ac.uk/id/eprint/10045564 |
Archive Staff Only
![]() |
View Item |