HDL Remodeling During the Acute Phase Response

被引:122
作者
Jahangiri, Anisa [1 ,4 ,5 ]
de Beer, Maria C. [3 ,4 ,5 ]
Noffsinger, Victoria [1 ,4 ,5 ]
Tannock, Lisa R. [1 ,4 ,5 ,6 ]
Ramaiah, Chandrashekar [2 ]
Webb, Nancy R. [1 ,4 ,5 ]
van der Westhuyzen, Deneys R. [1 ,4 ,5 ]
de Beer, Frederick C. [1 ,4 ,5 ,6 ]
机构
[1] Univ Kentucky, Dept Internal Med, Div Endocrinol & Mol Med, Lexington, KY 40506 USA
[2] Univ Kentucky, Dept Surg, Lexington, KY 40506 USA
[3] Univ Kentucky, Dept Physiol, Lexington, KY 40506 USA
[4] Univ Kentucky, Cardiovasc Res Ctr, Lexington, KY 40506 USA
[5] Univ Kentucky, Grad Ctr Nutrit Sci, Lexington, KY 40506 USA
[6] Vet Affairs Hosp, Lexington, KY USA
关键词
SAA; HDL; CETP; apoA-I; inflammation; HIGH-DENSITY-LIPOPROTEIN; SERUM-AMYLOID-A; ESTER TRANSFER PROTEIN; SECRETORY PHOSPHOLIPASE A(2); REVERSE CHOLESTEROL TRANSPORT; ANTIINFLAMMATORY PROPERTIES; MESSENGER-RNA; METABOLISM; PLASMA; SIZE;
D O I
10.1161/ATVBAHA.108.178681
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-The purpose of this study was to examine the interactive action of serum amyloid A (SAA), group IIA secretory phospholipase A(2) (sPLA(2)-IIA), and cholesteryl ester transfer protein (CETP) on HDL remodeling and cholesterol efflux during the acute phase (AP) response elicited in humans after cardiac surgery. Methods and Results-Plasma was collected from patients before (pre-AP), 24 hours after (AP-1 d), and 5 days after cardiac surgery (AP-5 d). SAA levels were increased 16-fold in AP-1 d samples. The activity of sPLA(2)-IIA was increased from 77.7 +/- 38.3 U/mL (pre-AP) to 281.4 +/- 57.1 U/mL (AP-1 d; P < 0.001). CETP mass and activity reduction was commensurate to the reduction of HDL cholesterol levels. The combined action of SAA, sPLA(2)-IIA, and CETP in vitro markedly remodeled HDL with the generation of lipid-poor apoA-I from both pre-AP and AP-1 d HDL. The net result of this remodeling was a relative preservation of ABCA1-and ABCG1-dependent cholesterol efflux during the acute phase response. Conclusions-Our results show that the many and complex changes in plasma proteins during the acute phase response markedly remodel HDL with functional implications, particularly the relative retention of cholesterol efflux capacity. (Arterioscler Thromb Vasc Biol. 2009; 29: 261-267.)
引用
收藏
页码:261 / U194
页数:13
相关论文
共 37 条
[1]   Differential effects of HDL subpopulations on cellular ABCA1- and SR-BI-mediated cholesterol efflux [J].
Asztalos, BF ;
de la Llera-Moya, M ;
Dallal, GE ;
Horvath, KV ;
Schaefer, EJ ;
Rothblat, GH .
JOURNAL OF LIPID RESEARCH, 2005, 46 (10) :2246-2253
[2]   Antiinflammatory properties of HDL [J].
Barter, PJ ;
Nicholls, S ;
Rye, KA ;
Anantharamaiah, GM ;
Navab, M ;
Fogelman, AM .
CIRCULATION RESEARCH, 2004, 95 (08) :764-772
[3]   Hugh Sinclair Lecture: The regulation and remodelling of HDL by plasma factors [J].
Barter, PJ .
ATHEROSCLEROSIS SUPPLEMENTS, 2002, 3 (04) :39-47
[4]   METABOLISM OF VERY LOW-DENSITY LIPOPROTEIN PROTEINS .1. PRELIMINARY IN-VITRO AND IN-VIVO OBSERVATIONS [J].
BILHEIMER, DW ;
LEVY, RI ;
EISENBERG, S .
BIOCHIMICA ET BIOPHYSICA ACTA, 1972, 260 (02) :212-+
[5]   Alterations in high-density lipoprotein metabolism and reverse cholesterol transport in insulin resistance and type 2 diabetes mellitus: role of lipolytic enzymes, lecithin : cholesterol acyltransferase and lipid transfer proteins [J].
Borggreve, SE ;
de Vries, R ;
Dullaart, RPF .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2003, 33 (12) :1051-1069
[6]  
CABANA VG, 1989, J LIPID RES, V30, P39
[7]  
COETZEE GA, 1986, J BIOL CHEM, V261, P9644
[8]  
de Beer FC, 2000, J LIPID RES, V41, P1849
[9]   A review of CETP and its relation to atherosclerosis [J].
de Grooth, GJ ;
Klerkx, AHEM ;
Stroes, ESG ;
Stalenhoef, AFH ;
Kastelein, JJP ;
Kuivenhoven, JA .
JOURNAL OF LIPID RESEARCH, 2004, 45 (11) :1967-1974
[10]  
deBeer FC, 1997, J LIPID RES, V38, P2232