Opposite effects of cholesteryl ester transfer protein and phospholipid transfer protein on the size distribution of plasma high density lipoproteins - Physiological relevance in alcoholic patients

被引:70
作者
Lagrost, L
Athias, A
Herbeth, B
GuyardDangremont, V
Artur, Y
Paille, F
Gambert, P
Lallemant, C
机构
[1] FAC MED,INSERM CJF 93 10,LAB BIOCHIM LIPOPROT,F-21033 DIJON,FRANCE
[2] LAB CTR MED PREVENT,CNRS URA 597,F-54500 VANDOEUVRE NANCY,FRANCE
[3] FAC MED & PHARM,FORMAT BIOCHIM PHARMACOL,F-21033 DIJON,FRANCE
[4] CHRU,HOP FOURNIER,CTR ALCOOL,F-54000 NANCY,FRANCE
关键词
D O I
10.1074/jbc.271.32.19058
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of the present study was to investigate the role of the cholesteryl ester transfer protein (CETP) and the phospholipid transfer protein (PLTP) in determining the size distribution of high density lipoproteins (ADL) in human plasma, Whereas both purified CETP and PLTP preparations were able to promote the size redistribution of isolated HDL(3), CETP favored the emergence of small HDL, while PLTP induced the formation of both small and large conversion products. When the total plasma lipoprotein fractions isolated from nine distinct subjects were incubated for 24 h at 37 degrees C with either purified PLTP or purified CETP, significant alterations in the relative proportions of the five distinct plasma HDL subpopulations, i.e., HDL(21) (9.71-12.90 nm), HDL(2a) (8.77-9.71 nm), HDL(3a) (8.17-8.77 nm), HDL(3b) (7.76-8.17 nm), and HDL(3c) (7.21-7.16 nm) were also observed, PLTP induced a significant increase in the relative abundance of HDL(2b) (8.66 +/- 2.34% versus 7.87 +/- 1.83% in controls; p < 0.01) and a significant decrease in the relative abundance of HDL(3a) (32.16 +/- 3.42% versus 37.87 +/- 2.62% in controls; p < 0.05). In contrast, CETP significantly reduced the relative proportion of HDL2a (33.03 +/- 2.53% versus 37.56 +/- 6.43% in controls; p < 0.01) but significantly increased the relative proportion of both HDL(3b) (21.36 +/- 6.97% versus 15.58 +/- 7.75% in controls; p < 0.01) and HDL(3b) (3.21 +/- 4.84% versus 1.13 +/- 0.56% in controls; p < 0.05). Finally, in order to assess further the physiological relevance of in vitro observations, CETP activity, PLTP activity, and HDL size distribution were determined in plasmas from 33 alcoholic patients entering a cessation program. Alcohol withdrawaI was associated with (i) a significant increase in plasma CETP activity (173.5 +/- 70.55 h/ml before versus 223.2 +/- 69.3%/h/ml after alcohol withdrawal, p = 0.0001), (ii) a significant reduction in plasma PLTP activity (473.9 +/- 203.7%/h/ml before versus 312.7 +/- 148.4%/h/ml after alcohol withdrawal, p = 0.0001), and (iii) a significant shift of large HDL(2b) and RDL(2a) toward small HDL(3b)and HDL(3c). On the one hand, changes in plasma CETP activity correlated negatively with changes in the proportion of HDL(2a) (r = -0.597, p = 0.0002) and positively with changes in the proportion of HDL(3b) (r = 0.457, p = 0.0075), On the other hand, changes in plasma PLTP activity correlated positively with changes in the proportion of RDL(2b) (r = 0.482, p = 0.0045) and negatively with changes in the proportion of HDL(3a) (r = -0.418, p = 0.0154), Taken together, data of the present study revealed that plasma PLTP and CETP can exert opposite effects on the size distribution of plasma HDL. PLTP can promote the formation of HDL(2b) particles at the expense of HDL(3a), while CETP can promote the formation of HDL(3b) particles at the expense of HDL(2a).
引用
收藏
页码:19058 / 19065
页数:8
相关论文
共 50 条
[1]   ETHANOL STIMULATES APOLIPOPROTEIN A-I SECRETION BY HUMAN HEPATOCYTES - IMPLICATIONS FOR A MECHANISM FOR ATHEROSCLEROSIS PROTECTION [J].
AMARASURIYA, RN ;
GUPTA, AK ;
CIVEN, M ;
HORNG, YC ;
MAEDA, T ;
KASHYAP, ML .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1992, 41 (08) :827-832
[2]   THE INTERACTION OF CHOLESTERYL ESTER TRANSFER PROTEIN AND UNESTERIFIED FATTY-ACIDS PROMOTES A REDUCTION IN THE PARTICLE-SIZE OF HIGH-DENSITY LIPOPROTEINS [J].
BARTER, PJ ;
CHANG, LBF ;
NEWNHAM, HH ;
RYE, KA ;
RAJARAM, OV .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1045 (01) :81-89
[3]   CHARACTERIZATION OF HUMAN HIGH-DENSITY LIPOPROTEINS BY GRADIENT GEL-ELECTROPHORESIS [J].
BLANCHE, PJ ;
GONG, EL ;
FORTE, TM ;
NICHOLS, AV .
BIOCHIMICA ET BIOPHYSICA ACTA, 1981, 665 (03) :408-419
[4]  
CHEUNG MC, 1984, J BIOL CHEM, V259, P2201
[5]  
CHEUNG MC, 1991, J LIPID RES, V32, P383
[6]   CHOLESTERYL ESTER TRANSFER PROTEIN AND HEPATIC LIPASE ACTIVITY PROMOTE SHEDDING OF APO A-I FROM HDL AND SUBSEQUENT FORMATION OF DISCOIDAL HDL [J].
CLAY, MA ;
NEWNHAM, HH ;
FORTE, TM ;
BARTER, PI .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1124 (01) :52-58
[7]   TRANSFER OF [C-14]PHOSPHATIDYLCHOLINE BETWEEN LIPOSOMES AND HUMAN-PLASMA HIGH-DENSITY LIPOPROTEIN - PARTIAL-PURIFICATION OF A TRANSFER-STIMULATING PLASMA FACTOR USING A RAPID TRANSFER ASSAY [J].
DAMEN, J ;
REGTS, J ;
SCHERPHOF, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1982, 712 (03) :444-452
[8]   EFFECT OF LIPOPROTEIN-FREE PLASMA ON THE INTERACTION OF HUMAN-PLASMA HIGH-DENSITY LIPOPROTEIN WITH EGG-YOLK PHOSPHATIDYLCHOLINE LIPOSOMES [J].
DAMEN, J ;
DIJKSTRA, J ;
REGTS, J ;
SCHERPHOF, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1980, 620 (01) :90-99
[9]   CHANGES IN PLASMA HIGH-DENSITY LIPOPROTEINS IN CHRONIC MALE ALCOHOLICS DURING AND AFTER ABUSE [J].
DANIELSSON, B ;
EKMAN, R ;
FEX, G ;
JOHANSSON, BG ;
KRISTENSSON, H ;
NILSSONEHLE, P ;
WADSTEIN, J .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1978, 38 (02) :113-119
[10]  
DECKELBAUM RJ, 1979, J BIOL CHEM, V254, P6079