共 52 条
Stem cell models of polyglutamine diseases and their use in cell-based therapies
被引:7
作者:

Siska, Evangelia K.
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机构:
Biohellenika Biotechnol Co, Thessaloniki 57001, Greece Biohellenika Biotechnol Co, Thessaloniki 57001, Greece

Koliakos, George
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h-index: 0
机构:
Biohellenika Biotechnol Co, Thessaloniki 57001, Greece
Aristotle Univ Thessaloniki, Sch Med, Biochem Lab, AHEPA Univ Hosp, Thessaloniki, Greece Biohellenika Biotechnol Co, Thessaloniki 57001, Greece

Petrakis, Spyros
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Biohellenika Biotechnol Co, Thessaloniki 57001, Greece Biohellenika Biotechnol Co, Thessaloniki 57001, Greece
机构:
[1] Biohellenika Biotechnol Co, Thessaloniki 57001, Greece
[2] Aristotle Univ Thessaloniki, Sch Med, Biochem Lab, AHEPA Univ Hosp, Thessaloniki, Greece
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.
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Univ Florida, Evelyn F & William L McKnight Brain Inst, Dept Neurosci, Gainesville, FL 32610 USA Univ Florida, Evelyn F & William L McKnight Brain Inst, Dept Neurosurg, Gainesville, FL 32610 USA

Srivastava, Arun
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Univ Florida, Div Cellular & Mol Therapy, Dept Pediat, Coll Med, Gainesville, FL 32610 USA Univ Florida, Evelyn F & William L McKnight Brain Inst, Dept Neurosurg, Gainesville, FL 32610 USA

Zhang, Jianyi
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Univ Florida, FCMU, Dept Hlth Serv Res Management & Policy HSRMP, Coll Publ Hlth & Hlth Profess, Gainesville, FL 32610 USA Univ Florida, Evelyn F & William L McKnight Brain Inst, Dept Neurosurg, Gainesville, FL 32610 USA

Steindler, Dennis A.
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Univ Florida, Evelyn F & William L McKnight Brain Inst, Dept Neurosurg, Gainesville, FL 32610 USA Univ Florida, Evelyn F & William L McKnight Brain Inst, Dept Neurosurg, Gainesville, FL 32610 USA

Zheng, Tong
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Univ Florida, Evelyn F & William L McKnight Brain Inst, Dept Neurosurg, Gainesville, FL 32610 USA Univ Florida, Evelyn F & William L McKnight Brain Inst, Dept Neurosurg, Gainesville, FL 32610 USA