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纹状体持续表达睫状神经营养因子对正常和R6/1小鼠的行为及基因表达产生负面影响。

Sustained striatal ciliary neurotrophic factor expression negatively affects behavior and gene expression in normal and R6/1 mice.

作者信息

Denovan-Wright Eileen M, Attis Marissa, Rodriguez-Lebron Edgardo, Mandel Ronald J

机构信息

Department of Pharmacology, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

J Neurosci Res. 2008 Jun;86(8):1748-57. doi: 10.1002/jnr.21636.

Abstract

Huntington's disease (HD) is a neurodegenerative disorder caused by an elongation of CAG repeats in the HD gene, which encodes a mutant copy of huntingtin with an expanded polyglutatmine repeat. Individuals who are affected by the disease suffer from motor, cognitive, and emotional impairments. Levels of certain striatal-enriched mRNAs decrease in both HD patients and transgenic HD mice prior to the development of motor symptoms and neuronal cell death. Ciliary neurotrophic factor (CNTF) has been shown to protect neurons against chemically induced toxic insults in vitro and in vivo. To test the hypothesis that CNTF might protect neurons from the negative effects of the mutant huntingtin protein in vivo, CNTF was continuously expressed following transduction of the striatum by recombinant adeno-associated viral vectors (rAAV2). Wild-type and R6/1 HD transgenic (R6/1) mice that received bilateral or unilateral intrastriatal injections of rAAV2-CNTF experienced weight loss. The CNTF-treated R6/1 HD transgenic mice experienced motor impairments at an earlier age than expected compared with age-matched control R6/1 HD transgenic animals. CNTF also caused abnormal behavior in WT mice. In addition to behavioral impairments, in situ hybridization showed that, in both WT and R6/1 mice, CNTF expression caused a significant decrease in the levels of striatal-enriched transcripts. Overall, continuous expression of striatal CNTF at the dose mediated by the expression cassette used in this study was detrimental to HD and wild-type mice.

摘要

亨廷顿舞蹈症(HD)是一种神经退行性疾病,由HD基因中CAG重复序列的延长引起,该基因编码一种具有扩展的多聚谷氨酰胺重复序列的突变型亨廷顿蛋白。受该疾病影响的个体患有运动、认知和情感障碍。在运动症状和神经元细胞死亡出现之前,HD患者和转基因HD小鼠纹状体中某些富集的mRNA水平都会下降。睫状神经营养因子(CNTF)已被证明在体外和体内可保护神经元免受化学诱导的毒性损伤。为了验证CNTF可能在体内保护神经元免受突变型亨廷顿蛋白负面影响的假设,通过重组腺相关病毒载体(rAAV2)转导纹状体后持续表达CNTF。接受双侧或单侧纹状体内注射rAAV2-CNTF的野生型和R6/1 HD转基因(R6/1)小鼠体重减轻。与年龄匹配的对照R6/1 HD转基因动物相比,经CNTF处理的R6/1 HD转基因小鼠在更早的年龄出现运动障碍。CNTF还导致野生型小鼠出现异常行为。除行为障碍外,原位杂交显示,在野生型和R6/1小鼠中,CNTF表达均导致纹状体富集转录本水平显著下降。总体而言,以本研究中使用的表达盒介导的剂量持续表达纹状体CNTF对HD小鼠和野生型小鼠均有害。

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