Mouse models for mitochondrial diseases

被引:25
|
作者
Ruzzenente, Benedetta [1 ]
Rotig, Agnes [1 ]
Metodiev, Metodi D. [1 ]
机构
[1] Univ Paris 05, INSERM U1163, Sorbonne Paris Cite, Inst Imagine, 24 Blvd Montparnasse, F-75015 Paris, France
关键词
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA; RESPIRATORY-CHAIN DEFICIENCY; C-OXIDASE DEFICIENCY; TRANSFER-RNA; HYPERTROPHIC CARDIOMYOPATHY; EMBRYONIC LETHALITY; OXPHOS DEFICIENCIES; LACTIC-ACIDOSIS; MODIFIED MICE; MUTATIONS;
D O I
10.1093/hmg/ddw176
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
Mitochondrial diseases are heterogeneous and incurable conditions typically resulting from deficient ATP production in the cells. Mice, owing to their genetic and physiological similarity to humans as well as their relatively easy maintenance and propagation, are extremely valuable for studying mitochondrial diseases and are also indispensable for the preclinical evaluation of novel therapies for these devastating conditions. Here, we review the recent exciting developments in the field focusing on mouse models for mitochondrial disease genes although models for genes not involved in the pathogenesis of mitochondrial disease and therapeutic proof-of-concept studies using mouse models are also discussed.
引用
收藏
页码:R115 / R122
页数:8
相关论文
共 50 条
  • [31] Human mitochondrial DNA diseases and Drosophila models
    Chen, Zhe
    Zhang, Fan
    Xu, Hong
    JOURNAL OF GENETICS AND GENOMICS, 2019, 46 (04) : 201 - 212
  • [32] Cell models and drug discovery for mitochondrial diseases
    Hu, Shuang-yi
    Zhuang, Qian-qian
    Qiu, Yue
    Zhu, Xu-fen
    Yan, Qing-feng
    JOURNAL OF ZHEJIANG UNIVERSITY-SCIENCE B, 2019, 20 (05): : 449 - 456
  • [33] Human mitochondrial DNA diseases and Drosophila models
    Zhe Chen
    Fan Zhang
    Hong Xu
    JournalofGeneticsandGenomics, 2019, 46 (04) : 201 - 212
  • [34] Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function
    Iommarini, Luisa
    Peralta, Susana
    Torraco, Alessandra
    Diaz, Francisca
    MITOCHONDRION, 2015, 22 : 96 - 118
  • [35] Mitochondrial transcription: Lessons from mouse models
    Peralta, Susana
    Wang, Xiao
    Moraes, Carlos T.
    BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, 2012, 1819 (9-10): : 961 - 969
  • [36] Illuminating mitochondrial translation through mouse models
    Hughes, Laetitia A.
    Rackham, Oliver
    Filipovska, Aleksandra
    HUMAN MOLECULAR GENETICS, 2024, 33 (R1) : R61 - R79
  • [37] Mouse models of mitochondrial complex I dysfunction
    Irwin, Michael H.
    Parameshwaran, Kodeeswaran
    Pinkert, Carl A.
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2013, 45 (01): : 34 - 40
  • [38] Mouse models of mitochondrial dysfunction and heart failure
    Russell, LK
    Finck, BN
    Kelly, DP
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2005, 38 (01) : 81 - 91
  • [39] Pterostilbene in Combination With Mitochondrial Cofactors Improve Mitochondrial Function in Cellular Models of Mitochondrial Diseases
    Suarez-Rivero, Juan M.
    Pastor-Maldonado, Carmen J.
    Romero-Gonzalez, Ana
    Gomez-Fernandez, David
    Povea-Cabello, Suleva
    Alvarez-Cordoba, Monica
    Villalon-Garcia, Irene
    Talaveron-Rey, Marta
    Suarez-Carrillo, Alejandra
    Munuera-Cabeza, Manuel
    Sanchez-Alcazar, Jose A.
    FRONTIERS IN PHARMACOLOGY, 2022, 13
  • [40] Mouse models of diseases of megakaryocyte and platelet homeostasis
    Catherine L. Carmichael
    Warren S. Alexander
    Mammalian Genome, 2011, 22 : 449 - 465