Eye-open at birth phenotype with reduced keratinocyte motility in LGR4 null mice
FEBS Lett 581(24):6 (2007) PMID 17850793
We observed a consistent eye-open at birth (EOB) phenotype in mouse pups homozygous for a leucine-rich repeat containing G-protein coupled receptor 4 (Lgr4) allele deleting the whole transmembrane domain coding region. An in vitro wound-healing scratch assay showed notably reduced keratinocyte motility in the null mice. Phalloidin staining of F-actin in the eyelid epidermis was also reduced. We also generated keratinocyte-specific Lgr4 deficient mice, circumventing the embryonic/neonatal lethality and kidney abnormalities. Most of the conditional Lgr4 knockout mice showed the EOB phenotype. Thus, Lgr4 might be a novel gene class regulating cell motility.
DOI: 10.1016/j.febslet.2007.08.064Version: za2963e q8za1 q8zbf q8zcd q8zd6 q8zeb q8zff q8zg8