Integrated Department of Immunology, National Jewish Health and University of Colorado Denver School of Medicine, Denver, CO 80206, USA.
Clin Immunol. 2011 Jul;140(1):102-16. doi: 10.1016/j.clim.2011.04.002. Epub 2011 Apr 14.
Hematopoietic humanized mice generated via transplantation of human hematopoietic stem cells (hHSCs) into immunodeficient mice are a valuable tool for studying development and function of the human immune system. This study was performed to generate a protocol that improves development and quality of humanized mice in the BALB/c-Rag2(null)Il2rγ(null) strain, testing route of injection, in vitro culture and freezing of hHSCs, types of cytokines in the culture, and co-injection of lineage-depleted CD34(-) cells. Specific hHSC culturing conditions and the addition of support cells were found to increase the frequency, and human hematopoietic chimerism, of humanized mice. The optimized protocol resulted in BALB/c-Rag2(null)Il2rγ(null) humanized mice displaying more consistent human hematopoietic and lymphoid engraftment. Thus, hematopoietic humanized mice generated on a BALB/c immunodeficient background represent a useful model to study the human immune system.
通过将人造血干细胞(hHSCs)移植到免疫缺陷小鼠中产生的造血人源化小鼠是研究人类免疫系统发育和功能的有价值的工具。本研究旨在制定一种方案,以提高 BALB/c-Rag2(null)Il2rγ(null) 品系中人源化小鼠的发育和质量,测试注射途径、hHSCs 的体外培养和冷冻、培养中的细胞因子类型以及谱系耗竭的 CD34(-) 细胞的共注射。特定的 hHSC 培养条件和支持细胞的添加被发现可增加人源化小鼠的频率和人造血嵌合体。优化的方案导致 BALB/c-Rag2(null)Il2rγ(null) 人源化小鼠表现出更一致的人造血和淋巴样植入。因此,在 BALB/c 免疫缺陷背景下生成的造血人源化小鼠代表了研究人类免疫系统的有用模型。