Hemmi Hiroaki, Hoshino Katsuaki, Kaisho Tsuneyasu
Laboratory for Immune Regulation, WPI Immunology Frontier Research Center, Osaka University, 3-1 Yamada-oka, Suita, Osaka, 565-0871, Japan.
Laboratory of Inflammatory Regulation, RIKEN Center for Integrative Medical Sciences, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa, 230-0045, Japan.
Methods Mol Biol. 2016;1423:247-53. doi: 10.1007/978-1-4939-3606-9_17.
Dendritic cells (DCs) are one of the key populations controlling immune responses. To establish a cell depletion system in vivo, human diphtheria toxin (DT) receptor (DTR) is transduced to the mice in which DTR is expressed under the control of a specific promoter. In these mice, DTR-expressing cells are inducibly depleted after DT injection. Using this system, analysis of mouse models in which DTR was expressed under the CD11c promoter has contributed to our knowledge of DC biology by depleting CD11c(+) cells. Other mouse models to inducibly eliminate specific DC subsets upon DT treatment have been also generated. Here, we describe a new mouse model in which the XCR1(+) DC subset is inducibly and transiently depleted in vivo.
树突状细胞(DCs)是控制免疫反应的关键细胞群体之一。为了在体内建立细胞清除系统,将人白喉毒素(DT)受体(DTR)转导到小鼠体内,其中DTR在特定启动子的控制下表达。在这些小鼠中,注射DT后可诱导表达DTR的细胞被清除。利用该系统,对在CD11c启动子控制下表达DTR的小鼠模型进行分析,通过清除CD11c(+)细胞,增进了我们对DC生物学的了解。还建立了其他小鼠模型,可在DT处理后诱导消除特定的DC亚群。在此,我们描述一种新的小鼠模型,其中XCR1(+) DC亚群在体内可被诱导且短暂清除。