Elastin is a major structural component of large elastic arteries and a principal determinant of arterial biomechanical properties. Elastin loss of function mutations in humans have been linked to the autosomal dominant disease supravalvular aortic stenosis, which is characterized by stenotic lesions in both the systemic and pulmonary circulations. To better understand how elastin insufficiency influences the pulmonary circulation, we evaluated pulmonary cardiovascular physiology in a unique set of transgenic and knockout mice with graded vascular elastin dosage (range 45-120% of wild-type). The central pulmonary arteries of elastin-insufficient mice had smaller internal diameters (P< 0.0001), thinner walls (P= 0.002), and increased opening angles (P= 0.002) compared to WT controls. Pulmonary circulatory pressures, measured by right ventricular catheterization, were significantly elevated in elastin insufficient mice (P< 0.0001) and showed an inverse correlation with elastin level. Although elastin-insufficient animals exhibited mild to moderate right ventricular hypertrophy (P= 0.0001) and intrapulmonary vascular remodeling, the changes were less than expected given the high right ventricular pressures and were attenuated when compared with those seen in hypoxia-induced models of pulmonary arterial hypertension. The absence of extensive pathological cardiac remodeling at the high pressures in these animals suggests a developmental adaptation designed to maintain right-sided cardiac output in a vascular system with altered elastin content.