Apolipoprotein E and neurological disease: therapeutic potential and pharmacogenomic interactions

被引:44
作者
Tlaskowitz, Daniel
Vitek, Michael P.
机构
[1] Duke Univ, Med Ctr, Dept Med Neurol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Neurobiol, Durham, NC 27710 USA
[3] Cognosci Inc, Res Triangle Pk, NC 27709 USA
关键词
apolipoprotein E; astrocytes; microglia; multiple; sclerosis; neuroinflammation; stroke; subarachnoid; hemorrhage; traumatic; brain injury;
D O I
10.2217/14E22416.8.8.959
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The apolipoprotein E (apoE) polymorphism is emerging as a uniquely important genetic modifier that affects functional outcome from both acute and chronic neurological injuries. Recent attention has focused on common denominator mechanisms by which apoE might affect brain injury and/or brain repair responses in clinically diverse diseases. Although endogenous apoE likely serves several adaptive functions in the injured CNS, there is growing evidence that its effect on modifying brain inflammatory responses and providing protection from excitotoxic injury may be central to its protective properties. A more complete understanding of the role that apoE plays in the injured brain has led to novel therapeutic strategies for both acute and chronic neurological disease.
引用
收藏
页码:959 / 969
页数:11
相关论文
共 120 条
[21]   Apolipoprotein-E allele-specific regulation of nitric oxide production [J].
Colton, CA ;
Brown, CM ;
Czapiga, M ;
Vitek, MP .
NITRIC OXIDE: NOVEL ACTIONS, DELETERIOUS EFFECTS AND CLINICAL POTENTIAL, 2002, 962 :212-225
[22]   APOLIPOPROTEIN-E, SURVIVAL IN ALZHEIMERS-DISEASE PATIENTS, AND THE COMPETING RISKS OF DEATH AND ALZHEIMERS-DISEASE [J].
CORDER, EH ;
SAUNDERS, AM ;
STRITTMATTER, WJ ;
SCHMECHEL, DE ;
GASKELL, PC ;
RIMMLER, JB ;
LOCKE, PA ;
CONNEALLY, PM ;
SCHMADER, KE ;
TANZI, RE ;
GUSELLA, JF ;
SMALL, GW ;
ROSES, AD ;
PERICAKVANCE, MA ;
HAINES, JL .
NEUROLOGY, 1995, 45 (07) :1323-1328
[23]   GENE DOSE OF APOLIPOPROTEIN-E TYPE-4 ALLELE AND THE RISK OF ALZHEIMERS-DISEASE IN LATE-ONSET FAMILIES [J].
CORDER, EH ;
SAUNDERS, AM ;
STRITTMATTER, WJ ;
SCHMECHEL, DE ;
GASKELL, PC ;
SMALL, GW ;
ROSES, AD ;
HAINES, JL ;
PERICAKVANCE, MA .
SCIENCE, 1993, 261 (5123) :921-923
[24]   APOE genotype influences acquisition and recall following traumatic brain injury [J].
Crawford, FC ;
Vanderploeg, RD ;
Freeman, MJ ;
Singh, S ;
Waisman, M ;
Michaels, L ;
Abdullah, L ;
Warden, D ;
Lipsky, R ;
Salazar, A ;
Mullan, MJ .
NEUROLOGY, 2002, 58 (07) :1115-1118
[25]  
CURTISS LK, 1976, J IMMUNOL, V116, P1452
[26]  
CURTISS LK, 1981, J IMMUNOL, V126, P1382
[27]  
de Bont N, 1999, J LIPID RES, V40, P680
[28]  
DONG LM, 1994, J BIOL CHEM, V269, P22358
[29]   Human apolipoprotein E4 domain interaction - Arginine 61 and glutamic acid 255 interact to direct the preference for very low density lipoproteins [J].
Dong, LM ;
Weisgraber, KH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (32) :19053-19057
[30]   Genetic predisposition in patients undergoing cardiopulmonary bypass surgery is associated with an increase of inflammatory cytokines [J].
Drabe, N ;
Zünd, G ;
Grünenfelder, J ;
Sprenger, M ;
Hoerstrup, SP ;
Bestmann, L ;
Maly, FE ;
Turina, M .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2001, 20 (03) :609-613