(Circulation. 1996;94:2046-2051.)
© 1996 American Heart Association, Inc.
Articles |
the Departments of Medicine and Pathology, University of Chicago (Ill).
Correspondence to Jeffrey M. Leiden, MD, PhD, Department of Medicine, University of Chicago, 5841 S Maryland Ave, Chicago, IL 60637.
Key Words: Editorials genes lipoproteins cholesterol
| Introduction |
|---|
70% and 20%, respectively, of the HDL protein. Some HDL particles contain only apo A-I, whereas others contain both apo A-1 and apo A-II. As described below, recent data suggest that these two classes of HDL particles may differ significantly in their antiatherogenic potential.5 6 HDL particles contain, in addition to apo A-I and apo A-II, smaller amounts of apo A-IV, apo E, apo C, and apo D. HDL can also associate with two important lipid transfer proteins: LCAT, which catalyzes the formation of CE and lysolecithin from UC and lecithin (phosphatidyl choline), and CETP, which promotes the transfer of CEs from HDL to LDL and VLDL in exchange for TG. In addition, HDL particles undergo modification of their core lipid composition after interaction with hepatic lipase.
|
This article has been cited by other articles:
![]() |
P. Benoit, F. Emmanuel, J. M. Caillaud, L. Bassinet, G. Castro, P. Gallix, J. C. Fruchart, D. Branellec, P. Denefle, and N. Duverger Somatic Gene Transfer of Human ApoA-I Inhibits Atherosclerosis Progression in Mouse Models Circulation, January 12, 1999; 99(1): 105 - 110. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. D Gerard and D. Collen Adenovirus gene therapy for hypercholesterolemia, thrombosis and restenosis Cardiovasc Res, September 1, 1997; 35(3): 451 - 458. [Full Text] [PDF] |
||||
|
Circulation Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1996 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |