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Authors
Faust, Travis EFeinberg, Philip A
O'Connor, Ciara
Kawaguchi, Riki
Chan, Andrew
Strasburger, Hayley
Frosch, Maximilian
Boyle, Margaret A
Masuda, Takahiro
Amann, Lukas
Knobeloch, Klaus-Peter
Prinz, Marco
Schaefer, Anne
Schafer, Dorothy P
Student Authors
Philip FeinbergAcademic Program
MD/PhDUMass Chan Affiliations
Brudnick Neuropsychiatric Research InstituteMorningside Graduate School of Biomedical Sciences
Neurobiology
Schafer Lab
Document Type
Journal ArticlePublication Date
2023-08-26
Metadata
Show full item recordAbstract
Cre/loxP technology has revolutionized genetic studies and allowed for spatial and temporal control of gene expression in specific cell types. Microglial biology has particularly benefited because microglia historically have been difficult to transduce with virus or electroporation methods for gene delivery. Here, we investigate five of the most widely available microglial inducible Cre lines. We demonstrate varying degrees of recombination efficiency, cell-type specificity, and spontaneous recombination, depending on the Cre line and inter-loxP distance. We also establish best practice guidelines and protocols to measure recombination efficiency, particularly in microglia. There is increasing evidence that microglia are key regulators of neural circuits and major drivers of a broad range of neurological diseases. Reliable manipulation of their function in vivo is of utmost importance. Identifying caveats and benefits of all tools and implementing the most rigorous protocols are crucial to the growth of the field and the development of microglia-based therapeutics.Source
Faust TE, Feinberg PA, O'Connor C, Kawaguchi R, Chan A, Strasburger H, Frosch M, Boyle MA, Masuda T, Amann L, Knobeloch KP, Prinz M, Schaefer A, Schafer DP. A comparative analysis of microglial inducible Cre lines. Cell Rep. 2023 Aug 26;42(9):113031. doi: 10.1016/j.celrep.2023.113031. Epub ahead of print. PMID: 37635351.DOI
10.1016/j.celrep.2023.113031Permanent Link to this Item
http://hdl.handle.net/20.500.14038/52572PubMed ID
37635351Related Resources
This article is based on a previously available preprint in bioRxiv, https://doi.org/10.1101/2023.01.09.523268Rights
Copyright © 2023 The Author(s). This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).; Attribution-NonCommercial-NoDerivatives 4.0 InternationalDistribution License
http://creativecommons.org/licenses/by-nc-nd/4.0/ae974a485f413a2113503eed53cd6c53
10.1016/j.celrep.2023.113031
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- Creative Commons
Except where otherwise noted, this item's license is described as Copyright © 2023 The Author(s). This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).