Catechol O-methyltransferase (COMT) mRNA expression in the dorsolateral prefrontal cortex of patients with schizophrenia

被引:118
作者
Matsumoto, M [1 ]
Weickert, CS [1 ]
Beltaifa, S [1 ]
Kolachana, B [1 ]
Chen, JS [1 ]
Hyde, TM [1 ]
Herman, MM [1 ]
Weinberger, DR [1 ]
Kleinman, JE [1 ]
机构
[1] NIMH, Clin Brain Disorders Branch, Intramural Res Program, Bethesda, MD 20892 USA
关键词
cortical layer; DLPFC; dopamine; functional Val/Met polymorphism; human brain; in situ hybridization histochemistry; pyramidal neuron;
D O I
10.1038/sj.npp.1300218
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Human prefrontal cortical neurons express catechol O-methyltransferase (COMT), an enzyme that inactivates the neurotransmitter dopamine. A functional polymorphism of COMT, Val(108/158) Met, affects prefrontal function, and the high-activity Val allele has been reported to be a genetic risk factor for schizophrenia. We used in situ hybridization histochemistry to measure mRNA levels of COMT in the dorsolateral prefrontal cortex (DLPFC) of patients with schizophrenia (N = 14) and of normal controls (N = 15). While the groups did not differ in terms of mean level of COMT mRNA, there was a significantly different laminar pattern of COMT mRNA expression in pyramidal neurons (F = 2.68, df = 4,108, P<0.04); patients with schizophrenia had relatively lower levels in the superficial (II/III) layers and higher levels in the intermediate/deep (IV/V) layers (P<0.01), while in controls, the expression was homogeneous across layers. Neither the mean level nor the laminar distribution of COMT mRNA was related to the Val(108/158) Met genotype, suggesting that the feedback regulation of mRNA level is not a compensation for the functional effect of the COMT polymorphism. The disease-related laminar difference of COMT expression may be involved in dysregulation of dopamine signaling circuits in the DLPFC of patients with schizophrenia.
引用
收藏
页码:1521 / 1530
页数:10
相关论文
共 66 条
[51]   Neonatal lesions of the medial temporal lobe disrupt prefrontal cortical regulation of striatal dopamine [J].
Saunders, RC ;
Kolachana, BS ;
Bachevalier, J ;
Weinberger, DR .
NATURE, 1998, 393 (6681) :169-171
[52]  
Selemon LD, 1998, J COMP NEUROL, V392, P402
[53]   Family-based association studies of monoaminergic gene polymorphisms among North Indians with schizophrenia [J].
Semwal, P ;
Prasad, S ;
Bhatia, T ;
Deshpande, SN ;
Wood, J ;
Nimgaonkar, VL ;
Thelma, BK .
MOLECULAR PSYCHIATRY, 2001, 6 (02) :220-224
[54]  
Sesack SR, 1998, J NEUROSCI, V18, P2697
[55]   SILVER-ENHANCED DIAMINOBENZIDINE SULFIDE (SEDS) - A TECHNIQUE FOR HIGH-RESOLUTION IMMUNOELECTRON MICROSCOPY DEMONSTRATED WITH MONOAMINE IMMUNOREACTIVITY IN MONKEY CEREBRAL-CORTEX AND CAUDATE [J].
SMILEY, JF ;
GOLDMANRAKIC, PS .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1993, 41 (09) :1393-1404
[56]   GENOMIC ORGANIZATION OF THE HUMAN CATECHOL O-METHYLTRANSFERASE GENE AND ITS EXPRESSION FROM 2 DISTINCT PROMOTERS [J].
TENHUNEN, J ;
SALMINEN, M ;
LUNDSTROM, K ;
KIVILUOTO, T ;
SAVOLAINEN, R ;
ULMANEN, I .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 223 (03) :1049-1059
[57]  
Torrey Edwin Fuller, 1983, Surviving Schizophrenia: A Family Manual
[58]   Characterization of extracellular dopamine clearance in the medial prefrontal cortex: Role of monoamine uptake and monoamine oxidase inhibition [J].
Wayment, HK ;
Schenk, JO ;
Sorg, BA .
JOURNAL OF NEUROSCIENCE, 2001, 21 (01) :35-44
[59]   Cognitive impairments in patients with schizophrenia displaying preserved and compromised intellect [J].
Weickert, TW ;
Goldberg, TE ;
Gold, JM ;
Bigelow, LB ;
Egan, MF ;
Weinberger, DR .
ARCHIVES OF GENERAL PSYCHIATRY, 2000, 57 (09) :907-913
[60]   MESOCORTICAL DOPAMINERGIC FUNCTION AND HUMAN COGNITION [J].
WEINBERGER, DR ;
BERMAN, KF ;
CHASE, TN .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1988, 537 :330-338