Division of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH.
Blood. 2015 Apr 23;125(17):2630-40. doi: 10.1182/blood-2014-11-570218. Epub 2015 Mar 11.
The model systems available for studying human hematopoiesis, malignant hematopoiesis, and hematopoietic stem cell (HSC) function in vivo have improved dramatically over the last decade, primarily due to improvements in xenograft mouse strains. Several recent reviews have focused on the historic development of immunodeficient mice over the last 2 decades, as well as their use in understanding human HSC and leukemia stem cell (LSC) biology and function in the context of a humanized mouse. However, in the intervening time since these reviews, a number of new mouse models, technical approaches, and scientific advances have been made. In this review, we update the reader on the newest and best models and approaches available for studying human malignant and normal HSCs in immunodeficient mice, including newly developed mice for use in chemotherapy testing and improved techniques for humanizing mice without laborious purification of HSC. We also review some relevant scientific findings from xenograft studies and highlight the continued limitations that confront researchers working with human HSC and LSC in vivo.
过去十年中,可用于研究人类造血、恶性造血和造血干细胞 (HSC) 体内功能的模型系统有了显著的改善,这主要得益于异种移植小鼠品系的改进。最近有几篇综述聚焦于过去 20 年来免疫缺陷小鼠的历史发展,以及它们在理解人类 HSC 和白血病干细胞 (LSC) 生物学和功能方面在人源化小鼠中的应用。然而,在这些综述发表后的这段时间里,已经取得了许多新的小鼠模型、技术方法和科学进展。在这篇综述中,我们更新了读者关于在免疫缺陷小鼠中研究人类恶性和正常 HSC 的最新和最佳模型和方法的信息,包括用于化疗测试的新开发的小鼠以及无需繁琐的 HSC 纯化即可实现小鼠人源化的改进技术。我们还回顾了异种移植研究中的一些相关科学发现,并强调了从事人类 HSC 和 LSC 体内研究的研究人员所面临的持续限制。