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Parasympathetic innervation regulates tubulogenesis in the developing salivary gland.

TitleParasympathetic innervation regulates tubulogenesis in the developing salivary gland.
Publication TypeJournal Article
Year of Publication2014
AuthorsNedvetsky PI, Emmerson E, Finley JK, Ettinger A, Cruz-Pacheco N, Prochazka J, Haddox CL, Northrup E, Hodges C, Mostov KE, Hoffman MP, Knox SM
JournalDev Cell
Volume30
Issue4
Pagination449-62
Date Published2014 Aug 25
ISSN1878-1551
KeywordsAnimals, Apoptosis, Cyclic AMP, Cyclic AMP-Dependent Protein Kinases, Cystic Fibrosis Transmembrane Conductance Regulator, Epithelial Cells, Ganglia, Parasympathetic, Mice, Mice, Inbred ICR, Organogenesis, Salivary Ducts, Vasoactive Intestinal Peptide
Abstract

A fundamental question in development is how cells assemble to form a tubular network during organ formation. In glandular organs, tubulogenesis is a multistep process requiring coordinated proliferation, polarization and reorganization of epithelial cells to form a lumen, and lumen expansion. Although it is clear that epithelial cells possess an intrinsic ability to organize into polarized structures, the mechanisms coordinating morphogenetic processes during tubulogenesis are poorly understood. Here, we demonstrate that parasympathetic nerves regulate tubulogenesis in the developing salivary gland. We show that vasoactive intestinal peptide (VIP) secreted by the innervating ganglia promotes ductal growth, leads to the formation of a contiguous lumen, and facilitates lumen expansion through a cyclic AMP/protein kinase A (cAMP/PKA)-dependent pathway. Furthermore, we provide evidence that lumen expansion is independent of apoptosis and involves the cystic fibrosis transmembrane conductance regulator (CFTR), a cAMP-regulated Cl(-) channel. Thus, parasympathetic innervation coordinates multiple steps in tubulogenesis during organogenesis.

DOI10.1016/j.devcel.2014.06.012
Alternate JournalDev. Cell
PubMed ID25158854
PubMed Central IDPMC4155578
Grant ListS10 RR26758 / RR / NCRR NIH HHS / United States
5R01DK091530 / DK / NIDDK NIH HHS / United States
S10 RR026758 / RR / NCRR NIH HHS / United States
R21 DE022951 / DE / NIDCR NIH HHS / United States
R00 DE018969 / DE / NIDCR NIH HHS / United States
5R00DE018969 / DE / NIDCR NIH HHS / United States
R01 DK091530 / DK / NIDDK NIH HHS / United States
5R01DK074398 / DK / NIDDK NIH HHS / United States
R21DE022951 / DE / NIDCR NIH HHS / United States
R01 DK074398 / DK / NIDDK NIH HHS / United States
Publication institute
CRM