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Article Abstract

This study investigates the maturation status of rat lung epithelial cells in interspecies chimeras generated via blastocyst complementation (BC) using Fgfr2b-knockout mouse embryos. In our previous study, we succeeded in generating rat-derived lung epithelium in interspecies chimeras using tetraploid complementation; however, the resulting cells remained immature and failed to support respiratory function. In this study, we established two Fgfr2b-KO mouse lines via CRISPR/Cas9 and injected GFP-labeled rat embryonic stem (ES) cells into blastocysts, which were then transferred to pseudopregnant female mice. Comparative histological analysis of airway spaces between wild-type rat lungs (E19.5-E21.5) and BC chimeras revealed that BC lungs reached a maturation stage comparable to E20.5-E21.5 rat lungs. Quantitative Polymerase Chain Reaction of key epithelial maturation markers-including ENaC subunits, Aqp5, and surfactant protein genes-demonstrated late-gestational upregulation in wild-type rat lungs, while expression levels in BC lungs exhibited significant inter-individual variability, corresponding to stages between E19.5 and E21.5 in wild-type rats. These findings suggest that the mouse host environment may partially promote maturation of rat-derived lung epithelial cells; however, additional mechanisms are likely required to achieve functional respiratory capacity.

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http://dx.doi.org/10.1111/gtc.70046DOI Listing

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