Abnormal expression of epidermal growth factor and its receptor in the forebrain and serum of schizophrenic patients

被引:125
作者
Futamura, T
Toyooka, K
Iritani, S
Niizato, K
Nakamura, R
Tsuchiya, K
Someya, T
Kakita, A
Takahashi, H
Nawa, H
机构
[1] Niigata Univ, Brain Res Inst, Dept Mol Biol, Niigata 9518585, Japan
[2] Niigata Univ, Sch Med, Dept Psychiat, Niigata 95021, Japan
[3] Matsuzawa Hosp, Tokyo, Japan
[4] Niigata Univ, Brain Res Inst, Pathol & Brain Dis Res Ctr, Niigata 95021, Japan
关键词
EGF; ErbB; striatum; haloperidol; postmortem brain; dopamine;
D O I
10.1038/sj.mp.4001081
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Epidermal growth factor (EGF) comprises a structurally related family of proteins containing heparin-binding EGF-like growth factor (HB-EGF) and transforming growth factor alpha (TGFalpha) that regulates the development of dopaminergic neurons as well as monoamine metabolism. We assessed the contribution of EGF to schizophrenia by measuring EGF family protein levels in postmortem brains and in fresh serum of schizophrenic patients and control subjects. EGF protein levels were decreased in the prefrontal cortex and striatum of schizophrenic patients, whereas the levels of HB-EGF and TGFa were not significantly different in any of the regions examined. Conversely, EGF receptor expression was elevated in the prefrontal cortex. Serum EGF levels were markedly reduced in schizophrenic patients, even in young, drug-free patients. Chronic treatment of animals with the antipsychotic drug haloperidol had no influence on EGF levels in the brain or serum. These findings suggest that there is abnormal EGF production in various central and peripheral tissues of patients with both acute and chronic schizophrenia. EGF might thus provide a molecular substrate for the pathologic manifestation of the illness, although additional studies are required to determine a potential link between impaired EGF signaling and the pathology/etiology of schizophrenia.
引用
收藏
页码:673 / 682
页数:10
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