The neuronal ceroid lipofuscinoses: Opportunities from model systems

被引:24
作者
Faller, Kiterie M. E. [1 ]
Gutierrez-Quintana, Rodrigo [1 ]
Mohammed, Alamin [3 ]
Rahim, Ahad A. [2 ]
Tuxworth, Richard I. [3 ]
Wager, Kim [4 ]
Bond, Michael [5 ]
机构
[1] Coll Vet Med & Life Sci, Sch Vet Med, Glasgow G61 1QH, Lanark, Scotland
[2] UCL Sch Pharm, London WC1N 1AX, England
[3] Univ Birmingham, Coll Med & Dent Sci, Birmingham B15 2TT, W Midlands, England
[4] Cardiff Univ, Cardiff Sch Biosci, Cardiff CF10 3AX, S Glam, Wales
[5] UCL, MRC Lab Mol Cell Biol, London WC1E 6BT, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2015年 / 1852卷 / 10期
关键词
Neuronal ceroid lipofuscinosis; NCL; Neurodegeneration; Model systems; JUVENILE BATTEN-DISEASE; CHRONOLOGICAL LIFE-SPAN; CYSTEINE-STRING PROTEIN; LYSOSOMAL STORAGE DISEASE; ENDOPLASMIC-RETICULUM STRESS; BONE-MARROW-TRANSPLANTATION; MITOCHONDRIAL ATP SYNTHASE; TRANSGENIC ZEBRAFISH MODEL; SOUTH HAMPSHIRE SHEEP; LARGE ANIMAL-MODEL;
D O I
10.1016/j.bbadis.2015.04.022
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
The neuronal ceroid lipofuscinoses are a group of severe and progressive neurodegenerative disorders, generally with childhood onset. Despite the fact that these diseases remain fatal, significant breakthroughs have been made in our understanding of the genetics that underpin these conditions. This understanding has allowed the development of a broad range of models to study disease processes, and to develop new therapeutic approaches. Such models have contributed significantly to our knowledge of these conditions. In this review we will focus on the advantages of each individual model, describe some of the contributions the models have made to our understanding of the broader disease biology and highlight new techniques and approaches relevant to the study and potential treatment of the neuronal ceroid lipofuscinoses. This article is part of a Special Issue entitled: "Current Research on the Neuronal Ceroid Lipofuscinoses (Batten Disease)". (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:2267 / 2278
页数:12
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