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人类慢性髓性白血病的衰老小鼠模型。

An aging mouse model of human chronic myeloid leukemia.

机构信息

Department of Cancer Biology, The Beckman Research Institute of City of Hope, Duarte, CA, USA.

Eugene and Ruth Roberts Summer Student Academy of City of Hope, Duarte, CA, USA.

出版信息

Oncogene. 2021 Apr;40(17):3152-3163. doi: 10.1038/s41388-021-01770-0. Epub 2021 Apr 6.

Abstract

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.

摘要

慢性髓细胞白血病(CML)是一种与年龄相关的血液恶性肿瘤。与许多其他与年龄相关的人类疾病一样,CML 的实验室动物研究使用的是年轻小鼠,没有考虑到衰老的影响。为了了解衰老如何影响人类年龄相关疾病的动物模型,我们在 75%存活率定义的老年 BALB/c 小鼠中建立了第一个人类 CML 的衰老小鼠模型。该模型通过非细胞毒性的骨髓谱系阳性细胞耗竭,然后进行 BCR-ABL 逆转录病毒转导和移植来建立。衰老小鼠中的 CML 与年轻小鼠中的 CML 有许多相似之处,但贫血的发生率更高,而贫血在人类 CML 中经常出现。重要的是,我们表明,供体造血干细胞和受者骨髓龛的衰老都影响了 BCR-ABL 介导的白血病发生和白血病谱。最佳的 CML 诱导依赖于供体和受者的年龄匹配,并且年轻和老年小鼠之间的交叉移植产生了不同白血病的混合物。因此,我们的模型为在衰老小鼠中进行 CML 建模的可行性和优点提供了初步证据,并为未来的 CML 干细胞耐药性和治疗干预研究提供了新工具,其中衰老将被视为一个影响因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d799/8087641/bd8fb5c46b48/nihms-1686871-f0001.jpg

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