Vascular origin determines angiotensin I-converting enzyme expression in endothelial cells

• Published in: Endothelium (New York, N.Y.) Vol. 5; no. 1; p. 73
• Main Authors: Baudin, B, Berard, M, Carrier, J L, Legrand, Y, Drouet, L
• Format: Journal Article
• Language: English
• Published: England 1997
• Subjects: Animals; Aorta, Thoracic; Brain - blood supply; Capillaries; Cell Membrane - enzymology; Cells, Cultured; Endothelium, Vascular - enzymology; Peptidyl-Dipeptidase A - analysis; Peptidyl-Dipeptidase A - metabolism; Peptidyl-Dipeptidase A - secretion; Pulmonary Artery; Swine; Vena Cava, Inferior; von Willebrand Diseases - enzymology
• ISSN: 1062-3329
• DOI: 10.3109/10623329709044160

Previous observations on the heterogeneous distribution of von Willebrand factor in the vascular endothelium led us to examine the expression of angiotensin I-converting enzyme (ACE) in function of the vascular origin of endothelial cells (EC). EC from pig thoracic aorta, pulmonary artery, inferior vena cava and brain capillaries were cultured and assayed for ACE by enzymatic radiochemical determination and by western-blot and immunofluorescence using an antiACE polyclonal antibody. EC from the various vascular levels secreted ACE in the culture medium; western-blot analysis showed its presence at cellular level and immunofluorescence confirmed its location on the plasma membrane. But quantification revealed that EC from pulmonary artery contain more ACE than EC from the other vessels, especially from brain capillaries; immunofluorescence correlated well with the functional data. In contrast, secretion of ACE by brain capillaries EC was faster than that of arteries and of vena cava, the latter being the less effective. This differential ACE expression along the vascular tree could have a pharmacological implication since ACE inhibitors, used in the treatment of arterial hypertension, may act more at the vascular level than on the plasma renin-angiotensin system. On the other hand, endothelial distribution of ACE was different from that of von Willebrand factor; in particular we showed that EC cultured from vessels of pigs homozygous for the von Willebrand disease, in which von Willebrand factor synthesis was completely abolished, normally express ACE.