Abstract | OBJECTIVE: Capillary isotachophoresis (cITP) is a technique for characterizing plasma lipoprotein subfractions according to their electrophoretic charges. We used this technique to examine the mechanism by which apoA-I/ phosphatidylcholine (POPC) discs increase pre-beta HDL. METHODS AND RESULTS: The cITP analysis was performed using plasma prestained with a lipophilic dye on a Beckman P/ACE MDQ system. Plasma from a patient with lecithin:cholesterol acyltransferase ( LCAT) deficiency who had increased apoE-containing HDL was used to characterize the charge distribution of apoA-I/POPC discs. cITP analysis of apoB- and E-depleted plasma of the patient in the presence of apoA-I/POPC discs indicated two major subfractions of apoA-I/POPC discs with mobilities of triglyceride-rich lipoproteins (fast and slow apoA-I). Incubation of whole plasma from a normolipidemic subject in the presence of apoA-I/POPC discs caused a reduction in cITP fast (f)- and intermediate (i)-migrating HDL, and fast and slow apoA-I, and an increase in slow (s)-migrating HDL. The changes in cITP lipoprotein subfractions were not affected by the inhibition of LCAT activity. ApoA-I/POPC discs increased the fractional esterification rate of cholesterol in apoB-depleted plasma. CONCLUSION:
ApoA-I/POPC discs remodeled cITP fHDL and iHDL to sHDL independent of LCAT activity.
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Authors | Bo Zhang, Shin-ichiro Miura, Ping Fan, Koichiro Kumagai, Kazuma Takeuchi, Yoshinari Uehara, Monica McMahon, Kerry-Anne Rye, Keijiro Saku |
Journal | Atherosclerosis
(Atherosclerosis)
Vol. 188
Issue 1
Pg. 95-101
(Sep 2006)
ISSN: 0021-9150 [Print] Ireland |
PMID | 16307746
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Apolipoprotein A-I
- High-Density Lipoproteins, Pre-beta
- Lipoproteins, HDL
- Phosphatidylcholines
- Phosphatidylcholine-Sterol O-Acyltransferase
- 1-palmitoyl-2-oleoylphosphatidylcholine
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Topics |
- Apolipoprotein A-I
(pharmacology)
- Electrophoresis, Capillary
(methods)
- High-Density Lipoproteins, Pre-beta
(blood)
- Humans
- Lecithin Cholesterol Acyltransferase Deficiency
(drug therapy)
- Lipoproteins, HDL
(drug effects)
- Monitoring, Physiologic
- Phosphatidylcholine-Sterol O-Acyltransferase
(antagonists & inhibitors)
- Phosphatidylcholines
(pharmacology)
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