Modulation of mechanosensitive genes during embryonic aortic arch development

Abstract

BackgroundEarly embryonic aortic arches (AA) are a dynamic vascular structures that are in the process of shaping into the great arteries of cardiovascular system. Previously, a time-lapsed mechanosensitive gene expression map was established for AA subject to altered mechanical loads in the avian embryo. To validate this map, we investigated effects on vascular microstructure and material properties following the perturbation of key genes using an in-house microvascular gene knockdown system.ResultsAll siRNA vectors show a decrease in the expression intensity of desired genes with no significant differences between vectors. In TGF beta 3 knockdowns, we found a reduction in expression intensities of TGF beta 3 (<= 76%) and its downstream targets such as ELN (<= 99.6%), Fbn1 (<= 60%), COL1 (<= 52%) and COL3 (<= 86%) and an increase of diameter in the left AA (23%). MMP2 knockdown also reduced expression levels in MMP2 (<= 30%) and a 6-fold increase in its downstream target COL3 with a decrease in stiffness of the AA wall and an increase in the diameter of the AA (55%). These in vivo measurements were confirmed using immunohistochemistry, western blotting and a computational growth model of the vascular extracellular matrix (ECM).ConclusionsLocalized spatial genetic modification of the aortic arch region governs the vascular phenotype and ECM composition of the embryo and can be integrated with mechanically-induced congenital heart disease models.