Pkd1 Regulates Lymphatic Vascular Morphogenesis during Development.


Autoria(s): Coxam, B.; Sabine, A.; Bower, N.I.; Smith, K.A.; Pichol-Thievend, C.; Skoczylas, R.; Astin, J.W.; Frampton, E.; Jaquet, M.; Crosier, P.S.; Parton, R.G.; Harvey, N.L.; Petrova, T.V.; Schulte-Merker, S.; Francois, M.; Hogan, B.M.
Data(s)

2014

Resumo

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.

Identificador

https://serval.unil.ch/notice/serval:BIB_075808604DCD

info:pmid:24767999

https://serval.unil.ch/resource/serval:BIB_075808604DCD.P001/REF

http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_075808604DCD9

urn:nbn:ch:serval-BIB_075808604DCD9

Idioma(s)

eng

Fonte

Cell Reports73623-633

Tipo

info:eu-repo/semantics/article

article

Formato

application/pdf

Direitos

info:eu-repo/semantics/openAccess

Copying allowed only for non-profit organizations

https://serval.unil.ch/disclaimer