AUTHOR=Chu Xuran , Taghizadeh Sara , Vazquez-Armendariz Ana Ivonne , Herold Susanne , Chong Lei , Chen Chengshui , Zhang Jin-San , El Agha Elie , Bellusci Saverio TITLE=Validation of a Novel Fgf10Cre–ERT2 Knock-in Mouse Line Targeting FGF10Pos Cells Postnatally JOURNAL=Frontiers in Cell and Developmental Biology VOLUME=9 YEAR=2021 URL=https://www.frontiersin.org/journals/cell-and-developmental-biology/articles/10.3389/fcell.2021.671841 DOI=10.3389/fcell.2021.671841 ISSN=2296-634X ABSTRACT=

Fgf10 is a key gene during development, homeostasis and repair after injury. We previously reported a knock-in Fgf10CreERT2 line (with the Cre-ERT2 cassette inserted in frame with the start codon of exon 1), called thereafter Fgf10Kiv1, to target FGF10Pos cells. While this line allowed fairly efficient and specific labeling of FGF10Pos cells during the embryonic stage, it failed to target these cells after birth, particularly in the postnatal lung, which has been the focus of our research. We report here the generation and validation of a new knock-in Fgf10CreERT2 line (called thereafter Fgf10Kiv2) with the insertion of the expression cassette in frame with the stop codon of exon 3. Fgf10Kiv2/+ heterozygous mice exhibited comparable Fgf10 expression levels to wild type animals. However, a mismatch between Fgf10 and Cre expression levels was observed in Fgf10Kiv2/+ lungs. In addition, lung and limb agenesis were observed in homozygous embryos suggesting a loss of Fgf10 functional allele in Fgf10Kiv2 mice. Bioinformatic analysis shows that the 3′UTR, where the Cre-ERT2 cassette is inserted, contains numerous putative transcription factor binding sites. By crossing this line with tdTomato reporter line, we demonstrated that tdTomato expression faithfully recapitulated Fgf10 expression during development. Importantly, Fgf10Kiv2 mouse is capable of significantly targeting FGF10Pos cells in the adult lung. Therefore, despite the aforementioned limitations, this new Fgf10Kiv2 line opens the way for future mechanistic experiments involving the postnatal lung.