Apolipoprotein A-II: Evaluating its significance in dyslipidaemia, insulin resistance, and atherosclerosis

被引:33
作者
Chan, Dick C. [1 ]
Ng, Theodore W. K. [2 ]
Watts, Gerald F. [1 ]
机构
[1] Univ Western Australia, Sch Med & Pharmacol, Metab Res Ctr, Perth, WA 6847, Australia
[2] Baker IDI Heart & Diabet Inst, Metab Lab, Melbourne, Vic, Australia
关键词
ApoA-II; cardiovascular disease; HDL transport; metabolic syndrome; HIGH-DENSITY-LIPOPROTEIN; CORONARY-HEART-DISEASE; BODY-MASS INDEX; APOA-II; TRANSGENIC MICE; HEPATIC LIPASE; HDL CHOLESTEROL; IN-VITRO; LPA-I; THERAPEUTIC TARGET;
D O I
10.3109/07853890.2011.573498
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Reduced HDL cholesterol, commonly found in subjects with obesity and type 2 diabetes, is associated with increased risk of cardiovascular disease (CVD). ApoA-II, a constituent apolipoprotein of certain HDL particles, plays an important role in the regulation of cholesterol efflux, HDL remodelling, and cholesteryl ester uptake via its interactions with lipid transfer proteins, lipases, and cellular HDL receptors. Recent studies have linked apoA-II directly with triglyceride and glucose metabolism. Most of the data are, however, derived from cellular systems and transgenic animal models. Direct evidence from human studies is scarce. Clinical studies demonstrate that apoA-II is a strong predictor of risk for CVD. There is no evidence, however, that selective therapeutic modification of apoA-II impacts on atherosclerosis and clinical outcomes. More research is required to investigate further the significance of apoA-II in clinical medicine.
引用
收藏
页码:313 / 324
页数:12
相关论文
共 109 条
[61]   DNA binding specificity and transactivation properties of SREBP-2 bound to multiple sites on the human apoA-II promoter [J].
Kan, HY ;
Pissios, P ;
Chambaz, J ;
Zannis, VI .
NUCLEIC ACIDS RESEARCH, 1999, 27 (04) :1104-1117
[62]   Expression of Human ApoAII in Transgenic Rabbits Leads to Dyslipidemia A New Model for Combined Hyperlipidemia [J].
Koike, Tomonari ;
Kitajima, Shuji ;
Yu, Ying ;
Li, Ying ;
Nishijima, Kazutoshi ;
Liu, Enqi ;
Sun, Huijun ;
Waqar, Ahmed Bilal ;
Shibata, Nobumitsu ;
Inoue, Tomoriho ;
Wang, Yao ;
Zhang, Bo ;
Kobayashi, Junji ;
Morimoto, Masatoshi ;
Saku, Keijiro ;
Watanabe, Teruo ;
Fan, Jianglin .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2009, 29 (12) :2047-U148
[63]   Functionally defective high-density lipoprotein: A new therapeutic target at the crossroads of dyslipidemia, inflammation, and atherosclerosis [J].
Kontush, Anatol ;
Chapman, M. John .
PHARMACOLOGICAL REVIEWS, 2006, 58 (03) :342-374
[64]  
KOREN E, 1987, CLIN CHEM, V33, P38
[65]  
LADIAS JAA, 1992, J BIOL CHEM, V267, P15849
[66]  
LAGOCKI PA, 1980, J BIOL CHEM, V255, P3701
[67]  
LAGROST L, 1994, J BIOL CHEM, V269, P3189
[68]   New insights into the regulation of HDL metabolism and reverse cholesterol transport [J].
Lewis, GF ;
Rader, DJ .
CIRCULATION RESEARCH, 2005, 96 (12) :1221-1232
[69]   Disordered fat storage and mobilization in the pathogenesis of insulin resistance and type 2 diabetes [J].
Lewis, GF ;
Carpentier, A ;
Adeli, K ;
Giacca, A .
ENDOCRINE REVIEWS, 2002, 23 (02) :201-229
[70]  
LI WH, 1988, J LIPID RES, V29, P245