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发育性维生素D缺乏会改变成年大鼠的脑蛋白表达:对神经精神疾病的影响。

Developmental vitamin D deficiency alters brain protein expression in the adult rat: implications for neuropsychiatric disorders.

作者信息

Almeras Lionel, Eyles Darryl, Benech Philippe, Laffite Daniel, Villard Claude, Patatian Angela, Boucraut Jose, Mackay-Sim Alan, McGrath John, Féron François

机构信息

Neurobiologie des Interactions Cellulaires et Neurophysiopathologie, CNRS UMR 6184, Faculté de Médecine, Université de la Méditerranée, Marseille, France.

出版信息

Proteomics. 2007 Mar;7(5):769-80. doi: 10.1002/pmic.200600392.

DOI:10.1002/pmic.200600392
PMID:17295352
Abstract

An increased risk for multiple sclerosis and schizophrenia is observed at increasing latitude and in patients born in winter or spring. To explore a possible link between maternal vitamin D deficiency and these brain disorders, we examined the impact of prenatal hypovitaminosis D on protein expression in the adult rat brain. Vitamin D-deficient female rats were mated with vitamin D normal males. Pregnant females were kept vitamin D-deficient until birth whereupon they were returned to a control diet. At week 10, protein expression in the progeny's prefrontal cortex and hippocampus was compared with control animals using silver staining 2-D gels associated with MS and newly devised data mining software. Developmental vitamin D (DVD) deficiency caused a dysregulation of 36 brain proteins involved in several biological pathways including oxidative phosphorylation, redox balance, cytoskeleton maintenance, calcium homeostasis, chaperoning, PTMs, synaptic plasticity and neurotransmission. A computational analysis of these data revealed that (i) nearly half of the molecules dysregulated in our animal model have also been shown to be misexpressed in either schizophrenia and/or multiple sclerosis and (ii) an impaired synaptic network may be a consequence of mitochondrial dysfunction.

摘要

在纬度增加以及出生于冬季或春季的患者中,多发性硬化症和精神分裂症的风险会增加。为了探究母体维生素D缺乏与这些脑部疾病之间可能存在的联系,我们研究了产前维生素D缺乏对成年大鼠大脑蛋白质表达的影响。维生素D缺乏的雌性大鼠与维生素D正常的雄性大鼠交配。怀孕的雌性大鼠在分娩前一直保持维生素D缺乏状态,之后恢复正常饮食。在第10周时,使用与质谱联用的银染二维凝胶和新设计的数据挖掘软件,将子代前额叶皮质和海马体中的蛋白质表达与对照动物进行比较。发育性维生素D(DVD)缺乏导致36种参与多种生物学途径的脑蛋白失调,这些途径包括氧化磷酸化、氧化还原平衡、细胞骨架维持、钙稳态、伴侣蛋白、翻译后修饰、突触可塑性和神经传递。对这些数据的计算分析表明:(i)在我们的动物模型中失调的分子中,近一半在精神分裂症和/或多发性硬化症中也被证明表达异常;(ii)突触网络受损可能是线粒体功能障碍的结果。

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