人性化鼠标
先天免疫系统
免疫系统
生物
造血
免疫学
祖细胞
巨噬细胞
先天性淋巴细胞
髓样
川地34
干细胞
癌症研究
细胞生物学
体外
生物化学
作者
Anthony Rongvaux,Tim Willinger,Jan Martínek,Till Strowig,Sofia V. Gearty,Lino L. Teichmann,Yasuyuki Saito,Florentina Marches,Stephanie Halene,Karolina Palucka,Markus G. Manz,Richard A. Flavell
摘要
A mouse bearing multiple human cytokine genes enables in vivo development and function of various human innate immune cell types. Mice repopulated with human hematopoietic cells are a powerful tool for the study of human hematopoiesis and immune function in vivo. However, existing humanized mouse models cannot support development of human innate immune cells, including myeloid cells and natural killer (NK) cells. Here we describe two mouse strains called MITRG and MISTRG, in which human versions of four genes encoding cytokines important for innate immune cell development are knocked into their respective mouse loci. The human cytokines support the development and function of monocytes, macrophages and NK cells derived from human fetal liver or adult CD34+ progenitor cells injected into the mice. Human macrophages infiltrated a human tumor xenograft in MITRG and MISTRG mice in a manner resembling that observed in tumors obtained from human patients. This humanized mouse model may be used to model the human immune system in scenarios of health and pathology, and may enable evaluation of therapeutic candidates in an in vivo setting relevant to human physiology.
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