Wnt5 signaling in vertebrate pancreas development.

TitleWnt5 signaling in vertebrate pancreas development.
Publication TypeJournal Article
Year of Publication2005
AuthorsKim HJ, Schleiffarth JR, Jessurun J, Sumanas S, Petryk A, Lin S, Ekker SC
JournalBMC Biol
Volume3
Pagination23
Date Published2005 Oct 24
ISSN1741-7007
KeywordsAnimals, Base Sequence, Cell Movement, Embryo, Nonmammalian, Frizzled Receptors, Gene Expression Regulation, Developmental, In Situ Hybridization, Insulin, Islets of Langerhans, Mice, Mice, Knockout, Morphogenesis, Pancreas, Polymerase Chain Reaction, Proto-Oncogene Proteins, Receptors, G-Protein-Coupled, Recombinant Fusion Proteins, Signal Transduction, Transcription, Genetic, Transfection, Vertebrates, Wnt Proteins, Wnt-5a Protein, Xenopus, Zebrafish, Zebrafish Proteins
Abstract

BACKGROUND: Signaling by the Wnt family of secreted glycoproteins through their receptors, the frizzled (Fz) family of seven-pass transmembrane proteins, is critical for numerous cell fate and tissue polarity decisions during development.

RESULTS: We report a novel role of Wnt signaling in organogenesis using the formation of the islet during pancreatic development as a model tissue. We used the advantages of the zebrafish to visualize and document this process in living embryos and demonstrated that insulin-positive cells actively migrate to form an islet. We used morpholinos (MOs), sequence-specific translational inhibitors, and time-lapse imaging analysis to show that the Wnt-5 ligand and the Fz-2 receptor are required for proper insulin-cell migration in zebrafish. Histological analyses of islets in Wnt5a(-/-) mouse embryos showed that Wnt5a signaling is also critical for murine pancreatic insulin-cell migration.

CONCLUSION: Our results implicate a conserved role of a Wnt5/Fz2 signaling pathway in islet formation during pancreatic development. This study opens the door for further investigation into a role of Wnt signaling in vertebrate organ development and disease.

DOI10.1186/1741-7007-3-23
Alternate JournalBMC Biol
PubMed ID16246260
PubMed Central IDPMC1276788
Grant ListGM63904 / GM / NIGMS NIH HHS / United States
R01 GM063904-01 / GM / NIGMS NIH HHS / United States
R01 GM055877 / GM / NIGMS NIH HHS / United States
R01 GM063904 / GM / NIGMS NIH HHS / United States
R56 GM063904 / GM / NIGMS NIH HHS / United States
T32 GM008244 / GM / NIGMS NIH HHS / United States
5 T32 GM08244-16 / GM / NIGMS NIH HHS / United States
GM55877 / GM / NIGMS NIH HHS / United States
Related Faculty: 
Jose Jessurun, M.D.

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