Tamoxifen dosing for Cre-mediated recombination in experimental bronchopulmonary dysplasia

• Published in: Transgenic research Vol. 26; no. 1; pp. 165 - 170
• Main Authors: Ruiz-Camp, Jordi, Rodríguez-Castillo, José Alberto, Herold, Susanne, Mayer, Konstantin, Vadász, István, Tallquist, Michelle D., Seeger, Werner, Ahlbrecht, Katrin, Morty, Rory E.
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 01-02-2017; Springer Nature B.V
• Subjects: Animal Genetics and Genomics; Animals; Biomedical and Life Sciences; Biomedical Engineering/Biotechnology; Bronchopulmonary Dysplasia - chemically induced; Bronchopulmonary Dysplasia - genetics; Bronchopulmonary Dysplasia - pathology; Disease Models, Animal; Genetic Engineering; Humans; Hyperoxia - genetics; Hyperoxia - pathology; Integrases - genetics; Life Sciences; Lung - growth & development; Lung - pathology; Mice, Transgenic; Molecular Medicine; Oxygen Consumption - genetics; Plant Genetics and Genomics; Premature Birth - genetics; Premature Birth - pathology; Recombination, Genetic; Tamoxifen - pharmacology; Transgenics; Transgenic; Bronchopulmonary dysplasia; Tamoxifen; Lung; Hyperoxia
• ISSN: 0962-8819; 1573-9368
• DOI: 10.1007/s11248-016-9987-8

Bronchopulmonary dysplasia (BPD) is the most common complication of preterm birth characterized by blunted post-natal lung development. BPD can be modelled in mice by exposure of newborn mouse pups to elevated oxygen levels. Little is known about the mechanisms of perturbed lung development associated with BPD. The advent of transgenic mice, where genetic rearrangements can be induced in particular cell-types at particular time–points during organogenesis, have great potential to explore the pathogenic mechanisms at play during arrested lung development. Many inducible, conditional transgenic technologies available rely on the application of the estrogen-receptor modulator, tamoxifen. While tamoxifen is well-tolerated and has been widely employed in adult mice, or in healthy developing mice; tamoxifen is not well-tolerated in combination with hyperoxia, in the most widely-used mouse model of BPD. To address this, we set out to establish a safe and effective tamoxifen dosing regimen that can be used in newborn mouse pups subjected to injurious stimuli, such as exposure to elevated levels of environmental oxygen. Our data reveal that a single intraperitoneal dose of tamoxifen of 0.2 mg applied to newborn mouse pups in 10 μl Miglyol vehicle was adequate to successfully drive Cre recombinase-mediated genome rearrangements by the fifth day of life, in a murine model of BPD. The number of recombined cells was comparable to that observed in regular tamoxifen administration protocols. These findings will be useful to investigators where tamoxifen dosing is problematic in the background of injurious stimuli and mouse models of human and veterinary disease.