Irwin S A, Swain R A, Christmon C A, Chakravarti A, Weiler I J, Greenough W T
Beckman Institute, University of Illinois, Urbana 61801, USA.
Neurobiol Learn Mem. 2000 Jan;73(1):87-93. doi: 10.1006/nlme.1999.3914.
The Fragile-X mental retardation protein, the protein absent in Fragile-X syndrome, is synthesized near synapses upon neurotransmitter activation. Humans and mice lacking this protein exhibit abnormal dendritic spine lengths and numbers. Here we investigated Fragile-X protein levels in animals exposed to behavioral paradigms that induce neuronal morphological change. Fragile-X protein immunoreactivity was examined in visual cortices of rats reared in a complex environment for 10 or 20 days, motor cortices of rats trained on motor-skill tasks for 3 or 7 days, and either visual or motor cortices of inactive controls. Rats exposed to a complex environment for 20 days or trained for 7 days on motor-skill tasks exhibited increased Fragile-X protein immunoreactivity in visual or motor cortices, respectively. These results provide the first evidence for a behaviorally induced alteration of Fragile-X protein expression and are compatible with previous findings suggesting synaptic regulation of its expression. These results also strengthen the association of Fragile-X mental retardation protein expression with the alteration of synaptic structure.
脆性X智力低下蛋白是脆性X综合征中缺失的蛋白,在神经递质激活时于突触附近合成。缺乏这种蛋白的人类和小鼠表现出异常的树突棘长度和数量。在此,我们研究了暴露于诱导神经元形态变化的行为范式的动物体内的脆性X蛋白水平。在复杂环境中饲养10天或20天的大鼠视觉皮层、接受运动技能任务训练3天或7天的大鼠运动皮层以及非活动对照组的视觉或运动皮层中检测脆性X蛋白免疫反应性。暴露于复杂环境20天的大鼠或接受运动技能任务训练7天的大鼠,其视觉或运动皮层中的脆性X蛋白免疫反应性分别增加。这些结果首次证明了行为诱导的脆性X蛋白表达改变,并且与之前表明其表达受突触调节的研究结果一致。这些结果还加强了脆性X智力低下蛋白表达与突触结构改变之间的关联。