Characterization of apoA-IV-containing lipoprotein particles isolated from human plasma and interstitial fluid

65Citations
Citations of this article
18Readers
Mendeley users who have this article in their library.

Abstract

Apolipoprotein (apo) A-IV has been proposed to play a role in reverse cholesterol transport. ApoA-IVcontaining lipoprotein particles (A-IVLp) were isolated from human plasma and interstitial fluid and characterized by immunoaffinity chromatography. Two major A-IVLp subpopulations, lipoprotein particles containing apoA-IV with apoA-I (LpA-I:A-IV) and lipoprotein particles containing apoA-IV without apoA-I (LpA-IV), were identified. The larger subpopulation of A-IVLp is the LpA-IV that represents 70% (protein mass) of the initial particles. Only 5.8% of apoA-IVwas recovered in the retained fraction after affinity chromatography with an anti-apoA-I immunosorbent. ApoA-I, apoA-II, apoA-IV, apoB, apoC-III, apoD, apoE, apoH, lecithin : cholesterol acyltransferase (LCAT), cholesteryl ester transfer (CET) protein, proline-rich protein, and a protein of Mr 59,000 were detected in the A-IVLp. These particles contain more than 20% triglycerides (lipid mass). ApoA-IV-containing particles that were isolated from plasma are heterogeneous in size, consisting of two major populations with Stokes' diameters of 103 nm and 9.3 nm. Both subpopulations of A-IVLp contain LCAT and GET activities and promote cholesterol efflux from cholesterol-preloaded adipose cells. These data support the hypothesis that A-IVLp particles may be involved in reverse cholesterol transport.

Cite

CITATION STYLE

APA

Duverger, N., Ghalim, N., Ailhaud, G., Steinmetz, A., Fruchart, J. C., & Castro, G. (1993). Characterization of apoA-IV-containing lipoprotein particles isolated from human plasma and interstitial fluid. Arteriosclerosis, Thrombosis, and Vascular Biology, 13(1), 126–132. https://doi.org/10.1161/01.atv.13.1.126

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free