Caenorhabditis elegans as a Model System for Duchenne Muscular Dystrophy

被引:5
作者
Ellwood, Rebecca A. [1 ,2 ]
Piasecki, Mathew [1 ,2 ]
Szewczyk, Nathaniel J. [1 ,2 ,3 ,4 ]
机构
[1] Univ Nottingham, Med Res Council MRC Versus Arthrit, Ctr Musculoskeletal Ageing Res, Royal Derby Hosp, Derby DE22 3DT, England
[2] Nottingham Biomed Res Ctr, Natl Inst Hlth Res, Derby DE22 3DT, England
[3] Ohio Univ, Ohio Musculoskeletal & Neurol Inst, Athens, OH 45701 USA
[4] Ohio Univ, Dept Biomed Sci, Heritage Coll Osteopath Med, Athens, OH 45701 USA
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
DMD; C; elegans; dystrophin; muscle; CARBONIC-ANHYDRASE-III; MUSCLE DEGENERATION; MDX MOUSE; ALPHA-CATULIN; BK CHANNEL; DYSTROBREVIN; GENE; INHIBITION; EXPRESSION; INTEGRITY;
D O I
10.3390/ijms22094891
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 nematode worm Caenorhabditis elegans has been used extensively to enhance our understanding of the human neuromuscular disorder Duchenne Muscular Dystrophy (DMD). With new arising clinically relevant models, technologies and treatments, there is a need to reconcile the literature and collate the key findings associated with this model.
引用
收藏
页数:19
相关论文
共 105 条
[1]  
Altun Z. F., 2009, WORMATLAS
[2]   Metformin Reverses the Enhanced Myocardial SR/ER-Mitochondria Interaction and Impaired Complex I-Driven Respiration in Dystrophin-Deficient Mice [J].
Angebault, Claire ;
Panel, Mathieu ;
Lacote, Mathilde ;
Rieusset, Jennifer ;
Lacampagne, Alain ;
Fauconnier, Jeremy .
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2021, 8
[3]   SEROTONIN UPTAKE IN BLOOD-PLATELETS OF DUCHENNE MUSCULAR-DYSTROPHY PATIENTS [J].
ARORA, RC ;
KUNCL, RW ;
MORGAN, J ;
COHEN, L ;
MELTZER, HY .
MUSCLE & NERVE, 1987, 10 (04) :359-362
[4]   Pharmacological rescue of the dystrophin-glycoprotein complex in Duchenne and Becker skeletal muscle explants by proteasome inhibitor treatment [J].
Assereto, S ;
Stringara, S ;
Sotgia, F ;
Bonuccelli, G ;
Broccolini, A ;
Pedemonte, M ;
Traverso, M ;
Biancheri, R ;
Zara, F ;
Bruno, C ;
Lisanti, MP ;
Minetti, C .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2006, 290 (02) :C577-C582
[5]   Method for the assessment of neuromuscular integrity and burrowing choice in vermiform animals [J].
Bainbridge, C. ;
Schuler, A. ;
Vidal-Gadea, A. G. .
JOURNAL OF NEUROSCIENCE METHODS, 2016, 264 :40-46
[6]   Mitochondrial Ca2+ Transport: Mechanisms, Molecular Structures, and Role in Cells [J].
Belosludtsev, K. N. ;
Dubinin, M. V. ;
Belosludtseva, N. V. ;
Mironova, G. D. .
BIOCHEMISTRY-MOSCOW, 2019, 84 (06) :593-607
[7]   The burrowing behavior of the nematode Caenorhabditis elegans: a newassay for the study of neuromuscular disorders [J].
Beron, C. ;
Vidal-Gadea, A. G. ;
Cohn, J. ;
Parikh, A. ;
Hwang, G. ;
Pierce-Shimomura, J. T. .
GENES BRAIN AND BEHAVIOR, 2015, 14 (04) :357-368
[8]   Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission [J].
Bessou, C ;
Giugia, JB ;
Franks, CJ ;
Holden-Dye, L ;
Ségalat, L .
NEUROGENETICS, 1998, 2 (01) :61-72
[9]   Function and genetics of dystrophin and dystrophin-related proteins in muscle [J].
Blake, DJ ;
Weir, A ;
Newey, SE ;
Davies, KE .
PHYSIOLOGICAL REVIEWS, 2002, 82 (02) :291-329
[10]   Alternative Polyadenylation Directs Tissue-Specific miRNA Targeting in Caenorhabditis elegans Somatic Tissues [J].
Blazie, Stephen M. ;
Geissel, Heather C. ;
Wilky, Henry ;
Joshi, Rajan ;
Newbern, Jason ;
Mangone, Marco .
GENETICS, 2017, 206 (02) :757-774