McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.
Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.
eNeuro. 2019 Aug 26;6(4). doi: 10.1523/ENEURO.0448-18.2019. Print 2019 Jul/Aug.
Microglia are specialized brain-resident macrophages with important functions in health and disease. To improve our understanding of these cells, the research community needs genetic tools to identify and control them in a manner that distinguishes them from closely related cell types. We have targeted the recently discovered microglia-specific gene to generate knock-in mice expressing EGFP (JAX#031823) or CreERT2 (JAX#031820) for the identification and manipulation of microglia, respectively. Genetic characterization of the locus and qPCR-based analysis demonstrate correct positioning of the transgenes and intact expression of endogenous in the knock-in mouse models. Immunofluorescence analysis further shows that parenchymal microglia, but not other brain macrophages, are completely and faithfully labeled in the EGFP-line at different time points of development. Flow cytometry indicates highly selective expression of EGFP in CD11bCD45lo microglia. Similarly, immunofluorescence and flow cytometry analyses using a Cre-dependent reporter mouse line demonstrate activity of CreERT2 primarily in microglia upon tamoxifen administration with the caveat of activity in leptomeningeal cells. Finally, flow cytometric analyses reveal absence of EGFP expression and minimal activity of CreERT2 in blood monocytes of the and lines, respectively. These new transgenic lines extend the microglia toolbox by providing the currently most specific genetic labeling and control over these cells in the myeloid compartment of mice.
小胶质细胞是一种特化的大脑驻留巨噬细胞,在健康和疾病中具有重要功能。为了提高我们对这些细胞的理解,研究界需要遗传工具来识别和控制它们,使其与密切相关的细胞类型区分开来。我们已经针对最近发现的小胶质细胞特异性基因进行了靶向操作,生成了分别表达 EGFP(JAX#031823)或 CreERT2(JAX#031820)的 knock-in 小鼠,用于小胶质细胞的鉴定和操作。对该基因座的遗传特征分析和基于 qPCR 的分析表明,转基因的正确定位和内源性基因的完整表达在 knock-in 小鼠模型中。免疫荧光分析进一步表明,在不同发育时间点,实质小胶质细胞(而非其他脑巨噬细胞)完全且忠实地被 EGFP 线标记。流式细胞术表明,EGFP 在 CD11bCD45lo 小胶质细胞中高度选择性表达。同样,使用依赖 Cre 的报告小鼠系进行的免疫荧光和流式细胞术分析表明,在给予他莫昔芬后,CreERT2 主要在小胶质细胞中发挥活性,但在软脑膜细胞中有活性。最后,流式细胞术分析显示,在和 品系中,EGFP 表达缺失,CreERT2 的活性最小。这些新的转基因系通过在小鼠髓系中提供目前最特异性的遗传标记和对这些细胞的控制,扩展了小胶质细胞工具包。