Mitochondrial dysfunction in neurological disorders: Exploring mitochondrial transplantation

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作者
Pedro Norat
Sauson Soldozy
Jennifer D. Sokolowski
Catherine M. Gorick
Jeyan S. Kumar
Youngrok Chae
Kaan Yağmurlu
Francesco Prada
Melanie Walker
Michael R. Levitt
Richard J. Price
Petr Tvrdik
M. Yashar S. Kalani
机构
[1] University of Virginia Health System,Department of Neurological Surgery
[2] University of Virginia School of Medicine,Department of Biomedical Engineering
[3] University of Washington School of Medicine,Department of Neurosurgery
[4] University of Virginia School of Medicine,Department of Neuroscience
[5] Fondazione IRCCS Istituto Neurologico Carlo Besta,Acoustic Neuroimaging and Therapy Laboratory
[6] Focused Ultrasound Foundation,undefined
[7] St. John’s Neuroscience Institute,undefined
来源
npj Regenerative Medicine | / 5卷
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摘要
Mitochondria are fundamental for metabolic homeostasis in all multicellular eukaryotes. In the nervous system, mitochondria-generated adenosine triphosphate (ATP) is required to establish appropriate electrochemical gradients and reliable synaptic transmission. Notably, several mitochondrial defects have been identified in central nervous system disorders. Membrane leakage and electrolyte imbalances, pro-apoptotic pathway activation, and mitophagy are among the mechanisms implicated in the pathogenesis of neurodegenerative diseases, such as Alzheimer’s, Parkinson’s, and Huntington’s disease, as well as ischemic stroke. In this review, we summarize mitochondrial pathways that contribute to disease progression. Further, we discuss pathological states that damaged mitochondria impose on normal nervous system processes and explore new therapeutic approaches to mitochondrial diseases.
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