Comparative analysis of CreER transgenic mice for the study of brain macrophages: A case study
- PMID: 31762013
- DOI: 10.1002/eji.201948342
Comparative analysis of CreER transgenic mice for the study of brain macrophages: A case study
Abstract
Conditional mutagenesis and fate mapping have contributed considerably to our understanding of physiology and pathology. Specifically, Cre recombinase-based approaches allow the definition of cell type-specific contributions to disease development and of inter-cellular communication circuits in respective animal models. Here we compared Cx3 cr1CreER and Sall1CreER transgenic mice and their use to decipher the brain macrophage compartment as a showcase to discuss recent technological advances. Specifically, we highlight the need to define the accuracy of Cre recombinase expression, as well as strengths and pitfalls of these particular systems that should be taken into consideration when applying these models.
Keywords: CreER; conditional mutagenesis; fate mapping; microglia; recombination.
© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
References
-
- Sauer, B. and Henderson, N., Site-specific DNA recombination in mammalian cells by the Cre recombinase of bacteriophage P1. Proc. Natl Acad. Sci. U.S.A. 1988. 85: 5166-5170.
-
- Metzger, D., Clifford, J., Chiba, H. and Chambon, P., Conditional site-specific recombination in mammalian cells using a ligand-dependent chimeric Cre recombinase. Proc. Natl Acad. Sci. U.S.A. 1995. 92: 6991-6995.
-
- Prinz, M., Jung, S. and Priller, J., Microglia biology: one century of evolving concepts. Cell 2019. 179: 292-311.
-
- Mrdjen, D., Pavlovic, A., Hartmann, F. J., Schreiner, B., Utz, S. G., Leung, B. P., Lelios, I. et al., High-dimensional single-cell mapping of central nervous system immune cells reveals distinct myeloid subsets in health, aging, and disease. Immunity 2018. 48: 380-395.e6.
-
- Goldmann, T., Wieghofer, P., Jordao, M. J. C., Prutek, F., Hagemeyer, N., Frenzel, K., Amann, L. et al., Origin, fate and dynamics of macrophages at central nervous system interfaces. Nat. Immunol. 2016. 17: 797-805.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Molecular Biology Databases