Stem cell models of polyglutamine diseases and their use in cell-based therapies

被引:7
|
作者
Siska, Evangelia K. [1 ]
Koliakos, George [1 ,2 ]
Petrakis, Spyros [1 ]
机构
[1] Biohellenika Biotechnol Co, Thessaloniki 57001, Greece
[2] Aristotle Univ Thessaloniki, Sch Med, Biochem Lab, AHEPA Univ Hosp, Thessaloniki, Greece
来源
关键词
polyglutamine; neurodegeneration; mesenchymal stem cells; cell model; transplantation; NEURAL PRECURSOR CELLS; HUNTINGTONS-DISEASE; MOUSE MODEL; SPINOCEREBELLAR ATAXIA; PURKINJE NEURONS; NEUROTROPHIC FACTORS; CEREBELLAR-ATAXIA; STROMAL CELLS; SCA1; FUSION;
D O I
10.3389/fnins.2015.00247
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Polyglutamine diseases are fatal neurological disorders that affect the central nervous system. They are caused by mutations in disease genes that contain GAG trinucleotide expansions in their coding regions. These mutations are translated into expanded glutamine chains in pathological proteins. Mutant proteins induce cytotoxicity, form intranuclear aggregates and cause neuronal cell death in specific brain regions. At the moment there is no cure for these diseases and only symptomatic treatments are available. Here, we discuss novel therapeutic approaches that aim in neuronal cell replacement using induced pluripotent or adult stem cells. Additionally, we present the beneficial effect of genetically engineered mesenchymal stem cells and their use as disease models or RNAi/gene delivery vehicles. In combination with their paracrine and cell-trophic properties, such cells may prove useful for the development of novel therapies against polyglutamine diseases.
引用
收藏
页数:8
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