학술논문

Hepatic Lipase Gene Therapy in Hepatic Lipase-deficient Mice: Adenovirus-mediated Replacement of a Lipolytic Enzyme to the Vascular Endothelium
Document Type
Academic Journal
Source
The Journal of Clinical Investigation. Feb 01, 1996 97(3):799-805
Subject
Language
English
ISSN
0021-9738
Abstract
Hepatic lipase (HL) is an endothelial-bound lipolytic enzyme which functions as a phospholipase as well as a triacylglycerol hydrolase and is necessary for the metabolism of IDL and HDL. To evaluate the feasibility of replacing an enzyme whose in vivo physiologic function depends on its localization on the vascular endothelium, we have infused recombinant replication-deficient adenovirus vectors expressing either human HL (HL-rAdV; n equals 7) or luciferase cDNA (Lucif-rAdV; n equals 4) into HL-deficient mice with pretreatment plasma cholesterol, phospholipid, and HDL cholesterol values of 176 plus minus 9, 314 plus minus 12, and 129 plus minus 9, respectively. After infusion of HL-rAdV, HL could be detected in the postheparin plasma of HL-deficient mice by immunoblotting and postheparin plasma HL activities were 25,700 plus minus 4,810 and 1,510 plus minus 688 nmol/min/ml on days 5 and 15, respectively. Unlike the mouse HL, 97% of the newly synthesized human HL was heparin releasable, indicating that the human enzyme was virtually totally bound to the mouse vascular endothelium. Infusion of HL-rAdV in HL-deficient mice was associated with a 50-80% decrease in total cholesterol, triglyceride, phospholipids, cholesteryl ester, and HDL cholesterol (P less than 0.001) as well as normalization of the plasma fast protein liquid chromatography lipoprotein profile by day 8. These studies demonstrate successful expression and delivery of a lipolytic enzyme to the vascular endothelium for ultimate correction of the HL gene defect in HL-deficient mice and indicate that recombinant adenovirus vectors may be useful in the replacement of endothelial-bound lipolytic enzymes in human lipolytic deficiency states. (J. Clin. Invest. 1996. 97:799-805.) Key words: gene therapy centered dot Adenoviridae centered dot hepatic lipase centered dot HDL centered dot phospholipid