遗传变异BDNF (Val66Met)对脑结构和功能的影响。

Zhe-Yu Chen, Kevin Bath, Bruce McEwen, Barbara Hempstead, Francis Lee
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引用次数: 116

摘要

人类脑源性神经营养因子(BDNF)基因中常见的单核苷酸多态性,即蛋氨酸(Met)在密码子66 (Val66Met)上替代缬氨酸(Val),与大脑解剖和记忆的改变有关,但其与临床疾病的相关性尚不清楚。我们产生了一种变异BDNF小鼠(BDNF(MET/ MET)),它复制了具有变异等位基因的人类的表型特征。变体BDNF(Met)在脑中的表达水平正常,但其在神经元中的分泌存在缺陷。在这种情况下,BDNF(Met/Met)小鼠代表了一种独特的模型,它将BDNF活性依赖性释放的改变与体内一系列确定的后果直接联系起来。我们对这些小鼠的后续分析阐明了一种在人类携带者中尚未建立的表型:焦虑增加。当被置于冲突环境中时,BDNF(Met/Met)小鼠表现出更多的焦虑相关行为,这些行为在抗抑郁药氟西汀的作用下是不正常的。因此,BDNF的遗传变异可能在焦虑和抑郁障碍的遗传易感性中起关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of genetic variant BDNF (Val66Met) on brain structure and function.

A common single-nucleotide polymorphism in the human brain-derived neurotrophic factor (BDNF) gene, a methionine (Met) substitution for valine (Val) at codon 66 (Val66Met), is associated with alterations in brain anatomy and memory, but its relevance to clinical disorders is unclear. We generated a variant BDNF mouse (BDNF(MET/Met)) that reproduces the phenotypic hallmarks in humans with the variant allele. Variant BDNF(Met) was expressed in brain at normal levels, but its secretion from neurons was defective. In this context, the BDNF(Met/Met) mouse represents a unique model that directly links altered activity-dependent release of BDNF to a defined set of in vivo consequences. Our subsequent analyses of these mice elucidated a phenotype that had not been established in human carriers: increased anxiety. When placed in conflict settings, BDNF(Met/Met) mice display increased anxiety-related behaviours that were not normalized by the antidepressant, fluoxetine. A genetic variant BDNF may thus play a key role in genetic predispositions to anxiety and depressive disorders.

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