Abstract P1111: A SOX17-PDGFB Signaling Axis Regulates Aortic Root Development

Abstract

Developmental etiologies causing complex congenital aortic root abnormalities are unknown. Here we show that deletion of Sox17 in aortic root endothelium in mice causes underdeveloped aortic root leading to a bicuspid aortic valve (BAV) due to the absence of non-coronary leaflet (NCL) and mispositioned left coronary ostium (LCO). The respective defects are associated with reduced proliferation of NCL mesenchyme and aortic root smooth muscle derived from the second heart field cardiomyocytes. Mechanistically, SOX17 occupies a Pdgfb transcriptional enhancer to promote its transcription and Sox17 deletion inhibits the endothelial Pdgfb transcription and PDGFB growth signaling to the NCL mesenchyme. Restoration of PDGFB in aortic root endothelium rescues the NCL and LCO defects in Sox17 nulls. These data support a SOX17-PDGFB axis underlying aortic root development that is critical for aortic valve and coronary ostium patterning, thereby informing a potential shared disease mechanism for concurrent anomalous aortic valve and coronary arteries.