Notch initiates the endothelial-to-mesenchymal transition in the atrioventricular canal through autocrine activation of soluble guanylyl cyclase.
Dev Cell, 2011/8/16;21(2):288-300.
Chang AC[1], Fu Y, Garside VC, Niessen K, Chang L, Fuller M, Setiadi A, Smrz J, Kyle A, Minchinton A, Marra M, Hoodless PA, Karsan A
Affiliations
PMID: 21839921DOI: 10.1016/j.devcel.2011.06.022
Impact factor: 13.417
Abstract
The heart is the most common site of congenital defects, and valvuloseptal defects are the most common of the cardiac anomalies seen in the newborn. The process of endothelial-to-mesenchymal transition (EndMT) in the cardiac cushions is a required step during early valve development, and Notch signaling is required for this process. Here we show that Notch activation induces the transcription of both subunits of the soluble guanylyl cyclase (sGC) heterodimer, GUCY1A3 and GUCY1B3, which form the nitric oxide receptor. In parallel, Notch also promotes nitric oxide (NO) production by inducing Activin A, thereby activating a PI3-kinase/Akt pathway to phosphorylate eNOS. We thus show that the activation of sGC by NO through a Notch-dependent autocrine loop is necessary to drive early EndMT in the developing atrioventricular canal (AVC).
MeSH terms
Animals; Cells, Cultured; Chromatin Immunoprecipitation; Endocardial Cushions; Endothelium; Female; Gene Expression Profiling; Guanylate Cyclase; Male; Mesoderm; Mice; Mice, Inbred C57BL; Mice, Knockout; Nitric Oxide Synthase Type III; Oligonucleotide Array Sequence Analysis; RNA Interference; Receptors, Cytoplasmic and Nuclear; Receptors, Notch; Signal Transduction; Soluble Guanylyl Cyclase
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