Comparative analysis of CreER transgenic mice for the study of brain macrophages: A case study

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 resp...

Full description

Saved in:
Bibliographic Details
Published inEuropean journal of immunology Vol. 50; no. 3; pp. 353 - 362
Main Authors Chappell‐Maor, Louise, Kolesnikov, Masha, Kim, Jung‐Seok, Shemer, Anat, Haimon, Zhana, Grozovski, Jonathan, Boura‐Halfon, Sigalit, Masuda, Takahiro, Prinz, Marco, Jung, Steffen
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 01.03.2020
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary: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 Cx3cr1CreER 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. Using the genetic manipulation of brain macrophages as example, we highlight the intricacies of the CreER model, including the dependence of recombination of celltype specificity and level of the CreER transgene expression, as well as the time window of expression.
Bibliography:https://publons.com/publon/10.1002/eji.201948342
See accompanying article
See accompanying article by Van Hove et al.
https://onlinelibrary.wiley.com/doi/abs/10.1002/eji.201948162
The peer review history for this article is available at
ISSN:0014-2980
1521-4141
DOI:10.1002/eji.201948342