免疫系统
先天免疫系统
免疫学
点头
造血
人性化鼠标
先天性淋巴细胞
生物
免疫
体内
干细胞
细胞生物学
生物技术
作者
Masashi Matsuda,Rintaro Ono,Tomonori Iyoda,Takaho A. Endo,Makoto Iwasaki,Mariko Tomizawa-Murasawa,Yoriko Saito,Akiko Kaneko,Kanako Shimizu,Daisuke Yamada,Narumi Ogonuki,Takashi Watanabe,Manabu Nakayama,Yoko Koseki,Fuyuko Kezuka-Shiotani,Takanori Hasegawa,Hiromasa Yabe,Shunichi Kato,Atsuo Ogura,Leonard D. Shultz
出处
期刊:Life science alliance
[Life Science Alliance]
日期:2019-04-01
卷期号:2 (2): e201800195-e201800195
被引量:63
标识
DOI:10.26508/lsa.201800195
摘要
The immune system encompasses acquired and innate immunity that matures through interaction with microenvironmental components. Cytokines serve as environmental factors that foster functional maturation of immune cells. Although NOD/SCID/IL2rgKO (NSG) humanized mice support investigation of human immunity in vivo, a species barrier between human immune cells and the mouse microenvironment limits human acquired as well as innate immune function. To study the roles of human cytokines in human acquired and innate immune cell development, we created NSG mice expressing hIL-7 and hIL-15. Although hIL-7 alone was not sufficient for supporting human NK cell development in vivo, increased frequencies of human NK cells were confirmed in multiple organs of hIL-7 and hIL-15 double knockin (hIL-7xhIL-15 KI) NSG mice engrafted with human hematopoietic stem cells. hIL-7xhIL-15 KI NSG humanized mice provide a valuable in vivo model to investigate development and function of human NK cells.
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