Cell reports · 2014
Pkd1 regulates lymphatic vascular morphogenesis during development.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Coxam Baptiste, Sabine Amélie, Bower Neil I, Smith Kelly A, Pichol-Thievend Cathy, Skoczylas Renae, Astin Jonathan W, Frampton Emmanuelle, Jaquet Muriel, Crosier Philip S, Parton Robert G, Harvey Natasha L, Petrova Tatiana V, Schulte-Merker Stefan, Francois Mathias, Hogan Benjamin M
Аннотация
Lymphatic vessels arise during development through sprouting of precursor cells from veins, which is regulated by known signaling and transcriptional mechanisms. The ongoing elaboration of vessels to form a network is less well understood. This involves cell polarization, coordinated migration, adhesion, mixing, regression, and shape rearrangements. We identified a zebrafish mutant, lymphatic and cardiac defects 1 (lyc1), with reduced lymphatic vessel development. A mutation in polycystic kidney disease 1a was responsible for the phenotype. PKD1 is the most frequently mutated gene in autosomal dominant polycystic kidney disease (ADPKD). Initial lymphatic precursor sprouting is normal in lyc1 mutants, but ongoing migration fails. Loss of Pkd1 in mice has no effect on precursor sprouting but leads to failed morphogenesis of the subcutaneous lymphatic network. Individual lymphatic endothelial cells display defective polarity, elongation, and adherens junctions. This work identifies a highly selective and unexpected role for Pkd1 in lymphatic vessel morphogenesis during development.
Предметные рубрики MeSH
AnimalsAnimals, Genetically ModifiedCells, CulturedEmbryo, MammalianEmbryonic DevelopmentEndothelial CellsHumansIntercellular JunctionsLymph NodesLymphangiogenesisLymphatic VesselsMiceMice, Inbred C57BLMice, TransgenicMutationPhenotypePolycystic Kidney, Autosomal DominantTRPP Cation ChannelsZebrafishZebrafish Proteins