Altered gene expression profiles in the frontal cortex of cirrhotic alcoholics

被引:51
作者
Liu, Jianwen
Lewohl, Joanne M.
Harris, R. Adron
Dodd, Peter R.
Mayfield, R. Dayne
机构
[1] Univ Texas, Waggoner Ctr Alcohol & Addict Res, Austin, TX 78712 USA
[2] Univ Queensland, Dept Biochem, St Lucia, Qld, Australia
关键词
cirrhosis; alcohol; brain; gene expression; microarray; CENTRAL-NERVOUS-SYSTEM; ADHESION MOLECULES; LIVER-DISEASE; AMMONIA NEUROTOXICITY; ASTROCYTES; MEMORY; BRAIN; EPIDEMIOLOGY; INHIBITION; MECHANISMS;
D O I
10.1111/j.1530-0277.2007.00444.x
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: Cirrhosis is the result of chronic liver disease that causes scarring and dysfunction of the liver. The disease is a common concomitant condition resulting from sustained exposure to alcohol. Heavy alcohol use results in brain damage that is generally more severe in cirrhotic compared with noncirrhotic alcoholics. We examined, at the cellular level, gene expression in the frontal cortex of cirrhotic alcoholics. Methods: Gene expression profiles were compared between cirrhotic and noncirrhotic alcoholics using similar to 47,000 element cDNA microarrays. Results: Widespread differences in transcriptome patterns were observed in cirrhotic compared with noncirrhotic alcoholics and these differences in gene expression accurately distinguished cirrhotic from noncirrhotic alcoholics. Functionally related groups of genes were identified that are involved in cell adhesion, mitochondrial function, synaptic transmission, apoptosis, and cell proliferation. Both astrocytes and neuronal cells were affected at the transcriptional level. The regulated genes are involved in neurite growth, neuronal cell adhesion, synaptic vesicle release, and postsynaptic neurotransmission. Conclusions: These changes in the transcriptome likely contribute to the more severe brain dysfunction in cirrhotic alcoholics.
引用
收藏
页码:1460 / 1466
页数:7
相关论文
共 47 条
[1]   THE ROLE OF CIRRHOSIS IN MEMORY FUNCTIONING OF ALCOHOLICS [J].
ARRIA, AM ;
TARTER, RE ;
KABENE, MA ;
LAIRD, SB ;
MOSS, H ;
VANTHIEL, DH .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1991, 15 (06) :932-937
[2]  
Aschner M, 2002, BRAIN PATHOL, V12, P475
[3]   Molecular diversity of astrocytes with implications for neurological disorders [J].
Bachoo, RM ;
Kim, RS ;
Ligon, KL ;
Maher, EA ;
Brennan, C ;
Billings, N ;
Chan, S ;
Li, C ;
Rowitch, DH ;
Wong, WH ;
DePinho, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (22) :8384-8389
[4]   Connections underlying the synthesis of cognition, memory, and emotion in primate prefrontal cortices [J].
Barbas, H .
BRAIN RESEARCH BULLETIN, 2000, 52 (05) :319-330
[5]   Neuropathological aspects of mitochondrial DNA disease [J].
Betts, J ;
Lightowlers, RN ;
Turnbull, DM .
NEUROCHEMICAL RESEARCH, 2004, 29 (03) :505-511
[6]   Expression pattern of NOGO-A protein in the human nervous system [J].
Buss, A ;
Sellhaus, B ;
Wolmsley, A ;
Noth, J ;
Schwab, ME ;
Brook, GA .
ACTA NEUROPATHOLOGICA, 2005, 110 (02) :113-119
[7]  
Butterworth R F, 1994, Alcohol Alcohol Suppl, V2, P259
[8]  
Butterworth RF, 2003, ALCOHOL RES HEALTH, V27, P240
[9]  
Chetri K, 2003, Indian J Gastroenterol, V22 Suppl 2, pS28
[10]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159