Overexpression of secretory phospholipase A2 causes rapid catabolism and altered tissue uptake of high density lipoprotein cholesteryl ester and apolipoprotein A-I

被引:137
作者
Tietge, UJF
Maugeais, C
Cain, W
Grass, D
Glick, JM
de Beer, FC
Rader, DJ
机构
[1] Univ Penn, Med Ctr, Dept Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Mol & Cellular Engn, Philadelphia, PA 19104 USA
[3] Univ Delaware, Dept Biol, Newark, DE 19716 USA
[4] Chrysalis DNX Transgen Sci, Princeton, NJ 08540 USA
[5] Univ Kentucky, Dept Internal Med, Lexington, KY 40536 USA
[6] Vet Affairs Med Ctr, Lexington, KY 40536 USA
关键词
D O I
10.1074/jbc.275.14.10077
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
Plasma levels of high density lipoprotein (HDL) cholesterol and its major protein component apolipoprotein (apo) A-I are significantly reduced in both acute and chronic inflammatory conditions, but the basis for this phenomenon is not well. understood, We hypothesized that secretory phospholipase A(2) (sPLA(2)), an acute phase protein that has been found in association with HDL, promotes HDL catabolism. A series of HDL metabolic studies were performed in transgenic mice that specifically overexpress human sPLA(2) but have no evidence of local or systemic inflammation, We found that HDL isolated from these mice have a significantly lower phospholipid and cholesteryl ester and significantly greater triglyceride content. The fractional catabolic rate (FCR) of I-125-HDL was significantly faster in sPLA(2) transgenic mice (4.08 +/- 0.01 pools/day) compared with control wildtype littermates (2.16 +/- 0.48 pools/day). I-125-HDL isolated from sPLA(2) transgenic mice was catabolized significantly faster than I-131-HDL isolated from wild-type mice after injection in wild-type mice (p < 0.001), Injection of I-125-tyramine-cellobiose-HDL demonstrated significantly greater degradation of HDL apolipoproteins in the kidneys of sPLA(2) transgenic mice compared with control mice (p < 0.05), The fractional catabolic rate of [H-3]cholesteryl ether HDL was significantly faster in sPLA(2)-overexpressing mice (6.48 +/- 0.24 pools/day) compared with controls (4.80 +/- 0.72 pools/day). Uptake of [H-3] cholesteryl ether into the livers and adrenals of sPLA(2) transgenic mice was significantly enhanced compared with control mice. In summary, these data demonstrate that overexpression of sPLA(2) alone in the absence of inflammation causes profound alterations of HDL metabolism in vivo and are consistent with the hypothesis that sPLA(2) may promote HDL catabolism in acute and chronic inflammatory conditions.
引用
收藏
页码:10077 / 10084
页数:8
相关论文
共 67 条
[1]  
ACTON S, 1996, SCIENCE, V271, P460
[2]   SAAM II: Simulation, Analysis, and Modeling Software for tracer and pharmacokinetic studies [J].
Barrett, PHR ;
Bell, BM ;
Cobelli, C ;
Golde, H ;
Schumitzky, A ;
Vicini, P ;
Foster, DM .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1998, 47 (04) :484-492
[3]   SERUM AMYLOID-A AND HIGH-DENSITY LIPOPROTEINS DURING THE ACUTE PHASE RESPONSE [J].
BAUSSERMAN, LL ;
BERNIER, DN ;
MCADAM, KPWJ ;
HERBERT, PN .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1988, 18 (06) :619-626
[4]  
BRESLOW JL, 1993, ANN NY ACAD SCI, V676, P157
[5]   ELEVATED HIGH-DENSITY LIPOPROTEIN CHOLESTEROL LEVELS CORRELATE WITH DECREASED APOLIPOPROTEIN-A-I AND APOLIPOPROTEIN-A-II FRACTIONAL CATABOLIC RATE IN WOMEN [J].
BRINTON, EA ;
EISENBERG, S ;
BRESLOW, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (01) :262-269
[6]   INCREASED APO-A-I AND APO-A-II FRACTIONAL CATABOLIC RATE IN PATIENTS WITH LOW HIGH-DENSITY LIPOPROTEIN-CHOLESTEROL LEVELS WITH OR WITHOUT HYPERTRIGLYCERIDEMIA [J].
BRINTON, EA ;
EISENBERG, S ;
BRESLOW, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (02) :536-544
[7]  
BROUSSEAU T, 1993, CLIN CHEM, V39, P960
[8]  
Cabana VG, 1996, J LIPID RES, V37, P2662
[9]   BEHAVIOR OF PHOSPHOLIPASE-MODIFIED HDL TOWARDS CULTURED-HEPATOCYTES .1. ENHANCED TRANSFERS OF HDL STEROLS AND APOPROTEINS [J].
COLLET, X ;
PERRET, BP ;
SIMARD, G ;
VIEU, C ;
DOUSTEBLAZY, L .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1043 (03) :301-310
[10]  
deBeer FC, 1997, J LIPID RES, V38, P2232