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提供健康的线粒体用于线粒体疾病及其他疾病的治疗。

Delivering healthy mitochondria for the therapy of mitochondrial diseases and beyond.

作者信息

Liu Chin-San, Chang Jui-Chih, Kuo Shou-Jen, Liu Ko-Hung, Lin Ta-Tsung, Cheng Wen-Ling, Chuang Sheng-Fei

机构信息

Vascular and Genomic Center, Changhua Christian Hospital, 135 Nanhsiao Street, Changhua 50094, Taiwan; Department of Neurology, Changhua Christian Hospital, 135 Nanhsiao Street, Changhua 50094, Taiwan; Graduate Institute of Integrated Medicine, College of Chinese Medicine, China Medical University, 91 Hsueh-Shih Road, Taichung 404, Taiwan.

Vascular and Genomic Center, Changhua Christian Hospital, 135 Nanhsiao Street, Changhua 50094, Taiwan.

出版信息

Int J Biochem Cell Biol. 2014 Aug;53:141-6. doi: 10.1016/j.biocel.2014.05.009. Epub 2014 May 16.

Abstract

Mitochondrial transfer has been demonstrated to a play a physiological role in the rescuing of mitochondrial DNA deficient cells by co-culture with human mesenchymal stem cells. The successful replacement of mitochondria using microinjection into the embryo has been revealed to improve embryo maturation. Evidence of mitochondrial transfer has been shown to minimize injury of the ischemic-reperfusion rabbit heart model. In this mini review, the therapeutic strategies of mitochondrial diseases based on the concept of mitochondrial transfer are illustrated, as well as a novel approach to peptide-mediated mitochondrial delivery. The possible mechanism of peptide-mediated mitochondrial delivery in the treatment of the myoclonic epilepsy and ragged-red fiber disease is summarized. Understanding the feasibility of mitochondrial manipulation in cells facilitates novel therapeutic skills in the future clinical practice of mitochondrial disorder.

摘要

线粒体转移已被证明在通过与人骨髓间充质干细胞共培养来拯救线粒体DNA缺陷细胞中发挥生理作用。已发现通过显微注射将线粒体成功导入胚胎可改善胚胎成熟度。线粒体转移的证据表明,它可使缺血再灌注兔心脏模型的损伤最小化。在这篇小型综述中,阐述了基于线粒体转移概念的线粒体疾病治疗策略,以及一种肽介导的线粒体递送新方法。总结了肽介导的线粒体递送在治疗肌阵挛性癫痫伴蓬毛样红纤维病中的可能机制。了解线粒体在细胞中操作的可行性有助于未来线粒体疾病临床实践中的新治疗技术发展。

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