Bernad Daniel M, Lachance Pascal E, Chaudhuri Avijit
University of Ottawa, Ottawa, Ontario, Canada.
Mcgill J Med. 2008 Jan;11(1):15-8.
During the early development of the visual cortex, there is a critical period when neuronal connections are highly sensitive to changes in visual input. Deprivation of visual stimuli during the critical period elicits robust anatomical and physiological rearrangements in the monkey visual cortex and serves as an excellent model for activity-dependent neuroplasticity. DNA microarray experiments were previously performed in our lab to analyze gene expression patterns in area V1 of vervet monkeys subjected to monocular deprivation (MD). An interesting candidate identified in its screen was myocyte enhancer-binding factor 2C (MEF2C), a transcription factor linked to neuronal survival. Consistent with the microarray data, we show that there is a qualitative increase in MEF2C protein expression in area V1 of infant as compared to adult vervet monkeys. Our results suggest that the regulation of neuronal survival is one of the molecular mechanisms underlying the critical period for visual cortical neuroplasticity.
在视觉皮层的早期发育过程中,存在一个关键期,在此期间神经元连接对视觉输入的变化高度敏感。在关键期剥夺视觉刺激会引发猴子视觉皮层中强烈的解剖学和生理学重排,并且是活动依赖性神经可塑性的一个优秀模型。我们实验室之前进行了DNA微阵列实验,以分析接受单眼剥夺(MD)的绿猴V1区的基因表达模式。在其筛选中鉴定出的一个有趣候选基因是肌细胞增强因子结合因子2C(MEF2C),这是一种与神经元存活相关的转录因子。与微阵列数据一致,我们表明,与成年绿猴相比,幼猴V1区MEF2C蛋白表达有质的增加。我们的结果表明,神经元存活的调节是视觉皮层神经可塑性关键期的分子机制之一。