Tmem119-EGFP and Tmem119-CreERT2 Transgenic Mice for Labeling and Manipulating Microglia.
Tobias KaiserGuoping FengPublished in: eNeuro (2019)
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 Tmem119 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 Tmem119 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 CD11b+CD45lo 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 Tmem119-EGFP and Tmem119-CreERT2 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.
Keyphrases
- inflammatory response
- flow cytometry
- neuropathic pain
- induced apoptosis
- poor prognosis
- cell cycle arrest
- genome wide
- healthcare
- mental health
- public health
- binding protein
- copy number
- signaling pathway
- dendritic cells
- oxidative stress
- gene expression
- bone marrow
- single cell
- mouse model
- resting state
- long non coding rna
- crispr cas
- endoplasmic reticulum stress
- white matter
- computed tomography
- pi k akt
- mesenchymal stem cells
- type diabetes
- patient safety
- skeletal muscle
- peripheral blood
- pet ct
- insulin resistance
- positron emission tomography
- bioinformatics analysis
- quality improvement
- health promotion
- subarachnoid hemorrhage