Decreased hippocampal expression of the susceptibility gene PPP3CC and other calcineurin subunits in schizophrenia

被引:60
作者
Eastwood, SL [1 ]
Burnet, PWJ [1 ]
Harrison, PJ [1 ]
机构
[1] Univ Oxford, Warneford Hosp, Dept Psychiat, Oxford OX3 7JX, England
基金
英国惠康基金;
关键词
calcineurin; gene expression; hippocampus; mRNA; PPP3CC; protein phosphatase 2B;
D O I
10.1016/j.biopsych.2004.12.029
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Calcineurin (CaN) is a phosphatase involved in synaptic plasticity. A haplotype of the PPP3CC gene, which encodes the gamma isoform of the catalytic subunit (CaN A), has been associated with schizophrenia. However, the distribution of CaN A gamma is not established, nor whether its expression changes in schizophrenia. Methods: CaN A expression was analyzed in the hippocampal formation of 13 patients with schizophrenia and 12 controls. All three isoforms were examined, using in situ hybridization histochemistry, RT-PCR, and laser-assisted microdissection. CaN A protein was assessed using ELISA and immunohistochemistry. CaN A mRNAs were also measured in rats treated with haloperidol or chlorpromazine. Results: CaN was prominent in excitatory neurons. CaN Act and A beta isoforms were abundant in all subfields, but CaN A gamma was not reliably detected in CA1. CaN A protein, and all three mRNAs, were decreased in schizophrenia. The mRNA reductions were present in all subfields measured, except CA1. CaN A mRNAs were unaltered in the antipsychotic-treated rats. Conclusions: Decreased CaN expression extends the evidence for aberrant hippocampal synaptic plasticity in schizophrenia, which particularly affects glulamatergic transmission, and which leaves CA1 relatively unaffected. Reduced expression of PPP3CC may underlie its genetic involvement in the disorder.
引用
收藏
页码:702 / 710
页数:9
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