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An aging mouse model of human chronic myeloid leukemia
Chronic myeloid leukemia (CML) is an age-dependent blood malignancy. Like many other age-dependent human diseases, laboratory animal research of CML uses young mice that do not factor in the influence of aging. To understand how aging may impact animal modeling of human age-dependent diseases, we es...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087641/ https://www.ncbi.nlm.nih.gov/pubmed/33824471 http://dx.doi.org/10.1038/s41388-021-01770-0 |
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author | Hao, Taisen Zhang, Chunxiao Wang, Zhiqiang Buck, Alison Vonderfecht, Steven L. Ermel, Richard Kim, Young Chen, WenYong |
author_facet | Hao, Taisen Zhang, Chunxiao Wang, Zhiqiang Buck, Alison Vonderfecht, Steven L. Ermel, Richard Kim, Young Chen, WenYong |
author_sort | Hao, Taisen |
collection | PubMed |
description | Chronic myeloid leukemia (CML) is an age-dependent blood malignancy. Like many other age-dependent human diseases, laboratory animal research of CML uses young mice that do not factor in the influence of aging. To understand how aging may impact animal modeling of human age-dependent diseases, we established the first aging mouse model of human CML in BALB/c mice in the advanced age defined by 75% survival. This model was developed by noncytotoxic depletion of bone marrow lineage-positive cells followed by BCR-ABL retroviral transduction and transplantation. CML developed in aging mice shared many similarities to that in young mice, but had increased incidence of anemia that is often seen in human CML. Importantly, we showed that aging of both donor hematopoietic stem cells and recipient bone marrow niche impacted BCR-ABL mediated leukemogenesis and leukemia spectrum. Optimal CML induction relied on age-matching for donors and recipients, and cross-transplantation between young and old mice produced a mixture of different leukemia. Therefore, our model provides initial evidence of the feasibility and merit of CML modeling in aging mice and offers a new tool for future studies of CML stem cell drug resistance and therapeutic intervention in which aging would be taken into consideration as an influencing factor. |
format | Online Article Text |
id | pubmed-8087641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-80876412021-10-06 An aging mouse model of human chronic myeloid leukemia Hao, Taisen Zhang, Chunxiao Wang, Zhiqiang Buck, Alison Vonderfecht, Steven L. Ermel, Richard Kim, Young Chen, WenYong Oncogene Article Chronic myeloid leukemia (CML) is an age-dependent blood malignancy. Like many other age-dependent human diseases, laboratory animal research of CML uses young mice that do not factor in the influence of aging. To understand how aging may impact animal modeling of human age-dependent diseases, we established the first aging mouse model of human CML in BALB/c mice in the advanced age defined by 75% survival. This model was developed by noncytotoxic depletion of bone marrow lineage-positive cells followed by BCR-ABL retroviral transduction and transplantation. CML developed in aging mice shared many similarities to that in young mice, but had increased incidence of anemia that is often seen in human CML. Importantly, we showed that aging of both donor hematopoietic stem cells and recipient bone marrow niche impacted BCR-ABL mediated leukemogenesis and leukemia spectrum. Optimal CML induction relied on age-matching for donors and recipients, and cross-transplantation between young and old mice produced a mixture of different leukemia. Therefore, our model provides initial evidence of the feasibility and merit of CML modeling in aging mice and offers a new tool for future studies of CML stem cell drug resistance and therapeutic intervention in which aging would be taken into consideration as an influencing factor. 2021-04-06 2021-04 /pmc/articles/PMC8087641/ /pubmed/33824471 http://dx.doi.org/10.1038/s41388-021-01770-0 Text en http://www.nature.com/authors/editorial_policies/license.html#termsUsers 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 Hao, Taisen Zhang, Chunxiao Wang, Zhiqiang Buck, Alison Vonderfecht, Steven L. Ermel, Richard Kim, Young Chen, WenYong An aging mouse model of human chronic myeloid leukemia |
title | An aging mouse model of human chronic myeloid leukemia |
title_full | An aging mouse model of human chronic myeloid leukemia |
title_fullStr | An aging mouse model of human chronic myeloid leukemia |
title_full_unstemmed | An aging mouse model of human chronic myeloid leukemia |
title_short | An aging mouse model of human chronic myeloid leukemia |
title_sort | aging mouse model of human chronic myeloid leukemia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087641/ https://www.ncbi.nlm.nih.gov/pubmed/33824471 http://dx.doi.org/10.1038/s41388-021-01770-0 |
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