Fiorini Claudia, Abdulhay Nour J, McFarland Sean K, Munschauer Mathias, Ulirsch Jacob C, Chiarle Roberto, Sankaran Vijay G
Division of Hematology/Oncology, The Manton Center for Orphan Disease Research, Boston Children's Hospital and Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
Am J Hematol. 2017 Sep;92(9):E513-E519. doi: 10.1002/ajh.24805. Epub 2017 Jul 19.
Immunodeficient mouse models have been valuable for studies of human hematopoiesis, but high-fidelity recapitulation of erythropoiesis in most xenograft recipients remains elusive. Recently developed immunodeficient and Kit mutant mice, however, have provided a suitable background to achieve higher-level human erythropoiesis after long-term hematopoietic engraftment. While there has been some characterization of human erythropoiesis in these models, a comprehensive analysis from various human developmental stages has not yet been reported. Here, we have utilized cell surface phenotypes, morphologic analyses, and molecular studies to fully characterize human erythropoiesis from multiple developmental stages in immunodeficient and Kit mutant mouse models following long-term hematopoietic stem and progenitor cell engraftment. We show that human erythropoiesis in such models demonstrates complete maturation and enucleation, as well as developmentally appropriate globin gene expression. These results provide a framework for future studies to utilize this model system for interrogating disorders affecting human erythropoiesis and for developing improved therapeutic approaches.
免疫缺陷小鼠模型对于人类造血研究具有重要价值,但在大多数异种移植受体中,红细胞生成的高保真重现仍然难以实现。然而,最近开发的免疫缺陷和Kit突变小鼠为长期造血植入后实现更高水平的人类红细胞生成提供了合适的背景。虽然在这些模型中已经对人类红细胞生成进行了一些表征,但尚未有来自不同人类发育阶段的综合分析报告。在这里,我们利用细胞表面表型、形态学分析和分子研究,对长期造血干细胞和祖细胞植入后的免疫缺陷和Kit突变小鼠模型中多个发育阶段的人类红细胞生成进行了全面表征。我们表明,此类模型中的人类红细胞生成表现出完全成熟和去核,以及发育上适当的珠蛋白基因表达。这些结果为未来利用该模型系统研究影响人类红细胞生成的疾病以及开发改进的治疗方法提供了框架。