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TiPS/TINS讲座。儿茶酚胺:从基因调控到神经精神疾病。

The TiPS/TINS Lecture. Catecholamines: from gene regulation to neuropsychiatric disorders.

作者信息

Mallet J

机构信息

Laboratoire de Génétique Moléculaire de la Neurotransmission et des Processus Neurodégénératifs (LGN), CNRS, Paris, France.

出版信息

Trends Neurosci. 1996 May;19(5):191-6. doi: 10.1016/s0166-2236(96)10029-1.

Abstract

In addition to their ability to change the electrical properties of neurons, evidence suggests that neurotransmitters are able to alter the cell's metabolism. Transmitter phenotype is labile and expression might be regulated, during development, by the cellular environment of neurons. The study of a key enzyme in the synthesis of catecholamines, tyrosine hydroxylase (TH), has provided clues about these adaptive responses. This enzyme has a large molecular diversity, resulting from the differential splicing of its mRNA, which is tissue-specific and might result in long-term changes in activity of the enzyme and, therefore, in the availability of neurotransmitter at various synapses. The presence of different DNA sequences at the TH locus confers susceptibility to various disorders of the brain, including manic-depressive illness and schizophrenia. Indeed, an association between a rare variant allele of the gene encoding TH and the occurrence of schizophrenia has been found in several populations. New techniques being developed to treat diseases such as Parkinson's disease involve various gene therapies, including a method of transferring genes directly into nerve cells using an adenovirus-based system.

摘要

除了能够改变神经元的电特性外,有证据表明神经递质能够改变细胞的新陈代谢。递质表型不稳定,在发育过程中,其表达可能受神经元细胞环境的调节。对儿茶酚胺合成中的一种关键酶——酪氨酸羟化酶(TH)的研究为这些适应性反应提供了线索。由于其mRNA的差异剪接,该酶具有很大的分子多样性,这种差异剪接具有组织特异性,可能导致该酶活性的长期变化,进而导致不同突触处神经递质的可用性发生变化。TH基因座上不同DNA序列的存在使人易患各种脑部疾病,包括躁郁症和精神分裂症。事实上,在多个群体中都发现了编码TH的基因的一种罕见变异等位基因与精神分裂症的发生之间存在关联。正在开发的用于治疗帕金森病等疾病的新技术涉及各种基因疗法,包括一种使用基于腺病毒的系统将基因直接导入神经细胞的方法。

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