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Published on: January 25, 2017
A novel Tmem119-tdTomato reporter mouse model for studying microglia in the central nervous system
Chunsheng Ruan1, Linlin Sun2, Alexandra Kroshilina1
1Center for Translational and Computational Neuroimmunology, Department of Neurology, Columbia University, New York, NY, USA; Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University, New York, NY, USA.
Abstract:
Microglia are resident immune cells of the central nervous system (CNS). The exact role of microglia in CNS disorders is not clear due to lack of tools to discriminate between microglia and infiltrating myeloid cells. Here, we present a novel reporter mouse model targeting a microglia-specific marker, TMEM119, for studying microglia in health and disease. By placing a reporter cassette (GSG-3xFlag-P2A-tdTomato) between the coding sequence of exon 2 and 3'UTR of the Tmem119 gene using CRISPR/Cas9 technology, we generated a Tmem119-tdTomato knock-in mouse strain. Gene expression assay showed no difference of endogenous Tmem119 in the CNS of Tmem119tdTomato/+ relative to wild-type mice. The cells expressing tdTomato were recognized by immunofluorescence staining using commercially available anti-TMEM119 antibodies. Additionally, immunofluorescence and flow cytometry techniques revealed that tdTomato+ cells are detected throughout the CNS, but not in peripheral tissues of Tmem119tdTomato/+ mice. Aging does not influence TMEM119 expression as tdTomato+ cells were detectable in the CNS of older mice (300 and 540 days old). Further immunofluorescence characterization shows that tdTomato+ cells colocalize with Iba1+ cells in the brain, but not with neurons, astrocytes or oligodendrocytes. Moreover, flow cytometry analysis of brain tissues of adult mice demonstrates that the majority of microglia CD45loCD11b+ cells (96.3%) are tdTomato-positive; and a minority of infiltrating CD45hiCD11b+ myeloid cells (5.3%) are also tdTomato-positive, which we further characterized and found that tdTomato expression is in part of choroid plexus macrophages but not in meningeal and perivascular macrophages. Functionally, using an acute injury model, we measured time-lapse activation of tdTomato-labeled microglia by transcranial two-photon microscopy in live Tmem119tdTomato/+ mice. Taken together, the Tmem119-tdTomato reporter mouse model is a valuable tool to specifically study the role of microglia in health and disease.
Insights
A novel reporter mouse model using TMEM119 specifically labels microglia in the central nervous system. This tool aids in distinguishing microglia from other myeloid cells, advancing research into neurological disorders.
Area of Science:
- Neuroscience
- Immunology
- Genetics
Background:
- Microglia are crucial immune cells in the central nervous system (CNS).
- Distinguishing microglia from infiltrating myeloid cells in CNS disorders is challenging.
- Lack of specific tools hinders the study of microglial roles in neurological diseases.
Purpose of the Study:
- To develop a novel reporter mouse model for specific microglia identification.
- To enable precise study of microglia in both healthy and diseased CNS conditions.
- To overcome limitations in discriminating microglia from peripheral myeloid cells.
Main Methods:
- Generated a Tmem119-tdTomato knock-in mouse model using CRISPR/Cas9.
- Utilized immunofluorescence and flow cytometry to validate tdTomato expression in microglia.
- Assessed tdTomato+ cell distribution in CNS and peripheral tissues, and across different ages.
- Analyzed colocalization with established cell markers (Iba1, CD45, CD11b).
Main Results:
- The Tmem119-tdTomato reporter accurately labels microglia throughout the CNS, including in aged mice.
- tdTomato+ cells represent the vast majority of microglia (CD45loCD11b+) and a small subset of myeloid cells (CD45hiCD11b+).
- Reporter mice allowed real-time monitoring of microglial activation in response to acute injury using two-photon microscopy.
Conclusions:
- The Tmem119-tdTomato mouse model provides a reliable method for specific microglia tracking.
- This tool facilitates detailed investigation of microglial function in CNS health and disease.
- Enables advanced studies on microglial dynamics and responses in vivo.

