Neuhofer Daniela, Henstridge Christopher M, Dudok Barna, Sepers Marja, Lassalle Olivier, Katona István, Manzoni Olivier J
INSERM U901 Marseille, France ; INMED Marseille, France ; Université de Aix-Marseille, UMR S901 Marseille, France.
Momentum Laboratory of Neurobiology, Institute of Experimental Medicine, Hungarian Academy of Sciences Budapest, Hungary.
Front Cell Neurosci. 2015 Mar 26;9:100. doi: 10.3389/fncel.2015.00100. eCollection 2015.
Fragile X is the most common cause of inherited intellectual disability and a leading cause of autism. The disease is caused by mutation of a single X-linked gene called fmr1 that codes for the Fragile X mental retardation protein (FMRP), a 71 kDa protein, which acts mainly as a translation inhibitor. Fragile X patients suffer from cognitive and emotional deficits that coincide with abnormalities in dendritic spines. Changes in spine morphology are often associated with altered excitatory transmission and long-term plasticity, the most prominent deficit in fmr1-/y mice. The nucleus accumbens, a central part of the mesocortico-limbic reward pathway, is now considered as a core structure in the control of social behaviors. Although the socio-affective impairments observed in Fragile X suggest dysfunctions in the accumbens, the impact of the lack of FMRP on accumbal synapses has scarcely been studied. Here we report for the first time a new spike timing-dependent plasticity paradigm that reliably triggers NMDAR-dependent long-term potentiation (LTP) of excitatory afferent inputs of medium spiny neurons (MSN) in the nucleus accumbens core region. Notably, we discovered that this LTP was completely absent in fmr1-/y mice. In the fmr1-/y accumbens intrinsic membrane properties of MSNs and basal excitatory neurotransmission remained intact in the fmr1-/y accumbens but the deficit in LTP was accompanied by an increase in evoked AMPA/NMDA ratio and a concomitant reduction of spontaneous NMDAR-mediated currents. In agreement with these physiological findings, we found significantly more filopodial spines in fmr1-/y mice by using an ultrastructural electron microscopic analysis of accumbens core medium spiny neuron spines. Surprisingly, spine elongation was specifically due to the longer longitudinal axis and larger area of spine necks, whereas spine head morphology and postsynaptic density size on spine heads remained unaffected in the fmr1-/y accumbens. These findings together reveal new structural and functional synaptic deficits in Fragile X.
脆性X综合征是遗传性智力障碍的最常见病因,也是自闭症的主要病因。该疾病由一个名为fmr1的X连锁单基因突变引起,该基因编码脆性X智力低下蛋白(FMRP),一种71 kDa的蛋白质,主要作为翻译抑制剂发挥作用。脆性X综合征患者存在认知和情感缺陷,这些缺陷与树突棘异常同时出现。脊柱形态的变化通常与兴奋性传递改变和长期可塑性有关,这是fmr1基因敲除小鼠最显著的缺陷。伏隔核是中脑边缘奖赏通路的核心部分,现在被认为是控制社会行为的核心结构。尽管在脆性X综合征中观察到的社会情感障碍表明伏隔核功能失调,但缺乏FMRP对伏隔核突触的影响几乎没有得到研究。在这里,我们首次报告了一种新的依赖于尖峰时间的可塑性范式,该范式可靠地触发伏隔核核心区域中棘神经元(MSN)兴奋性传入输入的NMDAR依赖的长时程增强(LTP)。值得注意的是,我们发现这种LTP在fmr1基因敲除小鼠中完全不存在。在fmr1基因敲除小鼠的伏隔核中,MSN的内在膜特性和基础兴奋性神经传递保持完整,但LTP缺陷伴随着诱发的AMPA/NMDA比值增加以及自发NMDAR介导电流的相应减少。与这些生理发现一致,通过对伏隔核核心中棘神经元棘进行超微结构电子显微镜分析,我们发现fmr1基因敲除小鼠中的丝状伪足棘明显更多。令人惊讶的是,脊柱伸长具体是由于脊柱颈部的纵轴更长和面积更大,而fmr1基因敲除小鼠的伏隔核中脊柱头部形态和脊柱头部的突触后致密物大小未受影响。这些发现共同揭示了脆性X综合征中新的结构和功能突触缺陷。