Kubat Gokhan Burcin, Ulger Oner, Akin Senay
Department of Exercise and Sports Physiology, Hacettepe University, Ankara, Turkey.
Department of Pathology, Gulhane Training and Research Hospital, Ankara, Turkey.
J Biochem Mol Toxicol. 2021 Nov;35(11):e22898. doi: 10.1002/jbt.22898. Epub 2021 Aug 25.
Maintenance of mitochondrial oxidative phosphorylation capacity and other mitochondrial functions are essential for the prevention of mitochondrial dysfunction-related diseases such as neurodegenerative, cardiovascular, and liver diseases. To date, no well-known treatment modality has been developed to prevent or reduce mitochondrial dysfunction. However, a novel approach that transplants fully functional mitochondria directly into defective cells has recently caught the attention of scientists. In this review, we provide an overview of the cell/tissue source of the mitochondria to prompt cell regeneration or tissue repair in vitro and in vivo applications. The animal and human models entail that effective procedures should be used in the isolation and confirmation of mitochondrial membrane potential and function. We believe that these procedures for mitochondrial transplantation for tissue or cell culture will confirm intact, viable, and free from contamination isolated mitochondria from the appropriate sources.
维持线粒体氧化磷酸化能力及其他线粒体功能对于预防与线粒体功能障碍相关的疾病(如神经退行性疾病、心血管疾病和肝脏疾病)至关重要。迄今为止,尚未开发出广为人知的预防或减少线粒体功能障碍的治疗方法。然而,一种将功能完备的线粒体直接移植到缺陷细胞中的新方法最近引起了科学家们的关注。在这篇综述中,我们概述了线粒体的细胞/组织来源,以促进其在体外和体内应用中的细胞再生或组织修复。动物和人类模型表明,在分离和确认线粒体膜电位及功能时应采用有效的程序。我们相信,这些用于组织或细胞培养的线粒体移植程序将确保从合适来源分离出完整、有活力且无污染的线粒体。