Mitochondrial transplantation as a promising therapy for mitochondrial diseases

被引:39
|
作者
Zhang, Tian-guang [1 ]
Miao, Chao-yu [1 ]
机构
[1] Second Mil Med Univ, Naval Med Univ, Dept Pharmacol, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
Mitochondria; Mitochondrial transplantation; Mitochondrial disease; Mitochondrial isolation; Mitochondrial delivery; Mitochondrial storage; Mitochondrial transplantation rejection; Ethical issue; FUNCTIONAL MITOCHONDRIA; RAT-BRAIN; REPERFUSION; INTERNALIZATION; MECHANISMS; DISORDERS; INJECTION; RESCUE;
D O I
10.1016/j.apsb.2022.10.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mitochondrial diseases are a group of inherited or acquired metabolic disorders caused by mitochondrial dysfunction which may affect almost all the organs in the body and present at any age. However, no satisfactory therapeutic strategies have been available for mitochondrial diseases so far. Mitochondrial transplantation is a burgeoning approach for treatment of mitochondrial diseases by recov-ery of dysfunctional mitochondria in defective cells using isolated functional mitochondria. Many models of mitochondrial transplantation in cells, animals, and patients have proved effective via various routes of mitochondrial delivery. This review presents different techniques used in mitochondrial isolation and de-livery, mechanisms of mitochondrial internalization and consequences of mitochondrial transplantation, along with challenges for clinical application. Despite some unknowns and challenges, mitochondrial transplantation would provide an innovative approach for mitochondrial medicine.(c) 2023 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:1028 / 1035
页数:8
相关论文
共 50 条
  • [31] The special considerations of gene therapy for mitochondrial diseases
    Slone, Jesse
    Huang, Taosheng
    NPJ GENOMIC MEDICINE, 2020, 5 (01)
  • [32] Therapeutic potential of pyruvate therapy for mitochondrial diseases
    Tanaka, Masashi
    Nishigaki, Yutaka
    Fuku, Noriyuki
    Ibi, Tohru
    Sahashi, Ko
    Koga, Yasutoshi
    MITOCHONDRION, 2007, 7 (06) : 399 - 401
  • [33] Alternative oxidase, a potential therapy for mitochondrial diseases
    Dassa, E. P.
    Halckaart, G. A. I.
    Dufour, E.
    Larsson, N. G.
    Jacobs, H. T.
    Rustin, P.
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2006, : 534 - 535
  • [34] Current advances in gene therapy of mitochondrial diseases
    Vladislav O. Soldatov
    Marina V. Kubekina
    Marina Yu. Skorkina
    Andrei E. Belykh
    Tatiana V. Egorova
    Mikhail V. Korokin
    Mikhail V. Pokrovskiy
    Alexey V. Deykin
    Plamena R. Angelova
    Journal of Translational Medicine, 20
  • [35] The special considerations of gene therapy for mitochondrial diseases
    Jesse Slone
    Taosheng Huang
    npj Genomic Medicine, 5
  • [36] Approaches and limitations to gene therapy for mitochondrial diseases
    Owen, R
    Flotte, TR
    ANTIOXIDANTS & REDOX SIGNALING, 2001, 3 (03) : 451 - 460
  • [37] Mitochondrial transplantation as a novel therapeutic strategy for cardiovascular diseases
    Mingchu Sun
    Wenhua Jiang
    Nan Mu
    Zihui Zhang
    Lu Yu
    Heng Ma
    Journal of Translational Medicine, 21
  • [38] Mitochondrial transplantation as a novel therapeutic strategy for cardiovascular diseases
    Sun, Mingchu
    Jiang, Wenhua
    Mu, Nan
    Zhang, Zihui
    Yu, Lu
    Ma, Heng
    JOURNAL OF TRANSLATIONAL MEDICINE, 2023, 21 (01)
  • [39] Strategies and Mechanisms of Mitochondrial Transplantation for Treating Neurological Diseases
    Zheng, Qian-Wen
    Yang, Yan-Ling
    Wang, Ya-Yun
    PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS, 2023, 50 (12) : 2925 - 2938
  • [40] The mitochondrial genome and human mitochondrial diseases
    Sukernik, RI
    Derbeneva, OA
    Starikovskaya, EB
    Volodko, NV
    Mikhailovskaya, IE
    Bychkov, IY
    Lott, M
    Brown, M
    Wallace, D
    RUSSIAN JOURNAL OF GENETICS, 2002, 38 (02) : 105 - 113