PLoS ONE · 2013 · 21 citations · 56 references
Life SciencesDevelopmental BiologyPhysiologyCell DifferentiationDevelopmental Cell BiologyEmbryogenesisCardiovascular DevelopmentCardiovascular Molecular PhysiologyEmbryonic Stem CellsHeart DevelopmentMuscle DifferentiationVascular DevelopmentCardiovascular BiologyEmbryonic Development GeneticsEmbryonic Lethality MutationsFetal Cardiovascular DevelopmentSmooth Muscle Cell DifferentiationVascular Smooth Muscle Cell PhysiologyVascular Smooth Muscle Cell ProliferationVasculogenesis
Members of the PRDM protein family have been shown to play important roles during embryonic development. Previous in vitro and in situ analyses indicated a function of Prdm6 in cells of the vascular system. To reveal physiological functions of Prdm6, we generated conditional Prdm6-deficient mice. Complete deletion of Prdm6 results in embryonic lethality due to cardiovascular defects associated with aberrations in vascular patterning. However, smooth muscle cells could be regularly differentiated from Prdm6-deficient embryonic stem cells and vascular smooth muscle cells were present and proliferated normally in Prdm6-deficient embryos. Conditional deletion of Prdm6 in the smooth muscle cell lineage using a SM22-Cre driver line resulted in perinatal lethality due to hemorrhage in the lungs. We thus identified Prdm6 as a factor that is essential for the physiological control of cardiovascular development.
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Establishment in culture of pluripotential cells from mouse embryos
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