Cell-and Gene-based Therapeutic Approaches for Neurological Deficits in Mucopolysaccharidoses

被引:0
作者
Pan, Dao [1 ,2 ]
机构
[1] Cincinnati Childrens Hosp, Med Ctr, Mol & Gene Therapy Program, Div Expt Hematol & Canc Biol, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Dept Pediat, Sch Med, Cincinnati, OH 45221 USA
基金
美国国家卫生研究院;
关键词
Mucopolysaccharidoses; central nervous system; blood-brain-barrier; animal models; stem cells; and gene therapy; PLURIPOTENT STEM-CELLS; BONE-MARROW-TRANSPLANTATION; IN-VIVO SELECTION; LYSOSOMAL STORAGE DISORDERS; CENTRAL-NERVOUS-SYSTEM; BLOOD-BRAIN-BARRIER; VII MOUSE-BRAIN; INACTIVATING LENTIVIRUS VECTOR; HEPARAN-SULFATE PROTEOGLYCANS; X-LINKED ADRENOLEUKODYSTROPHY;
D O I
10.2174/138920111795542679
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mucopolysaccharidoses (MPS) are a group of lysosomal storage diseases that are resulted from abnormal accumulation of glycosaminoglycans. Among the progressive multi-organ abnormalities often associated with MPS diseases, the deterioration of central nervous system (CNS) is the most challenging manifestations to be tackled, due to the impermeability of the blood-brain-barrier (BBB). Evolved with recent development in stem cell biotechnology and gene therapy, several novel experimental approaches have been investigated in animal models. In this review, we will address different approaches attempting to bypass the BBB for neuropathic MPS treatment using cell-and gene-based therapies. Several neurological findings in CNS pathophysiology emerged with therapeutic investigation will also be discussed.
引用
收藏
页码:884 / 896
页数:13
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