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Intercellular mitochondrial transfer in the brain, a new perspective for targeted treatment of central nervous system diseases

Journal

CNS NEUROSCIENCE & THERAPEUTICS
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1111/cns.14344

Keywords

central nervous system; mitochondrial transfer; targeted therapy

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This study aims to review the mechanism of mitochondrial transfer in the progress of central nervous system diseases and the possibility of targeted therapy. It found that various types of cells in the central nervous system can transfer mitochondria to each other through different pathways. Additionally, stress signals can trigger the transfer of mitochondria, and various molecular pathways and inhibitors can affect this process. Finally, the study proposes potential targeted pathways and treatment methods for regulating mitochondrial transfer in the treatment of related diseases.
AimMitochondria is one of the important organelles involved in cell energy metabolism and regulation and also play a key regulatory role in abnormal cell processes such as cell stress, cell damage, and cell canceration. Recent studies have shown that mitochondria can be transferred between cells in different ways and participate in the occurrence and development of many central nervous system diseases. We aim to review the mechanism of mitochondrial transfer in the progress of central nervous system diseases and the possibility of targeted therapy. MethodsThe PubMed databank, the China National Knowledge Infrastructure databank, and Wanfang Data were searched to identify the experiments of intracellular mitochondrial transferrin central nervous system. The focus is on the donors, receptors, transfer pathways, and targeted drugs of mitochondrial transfer. ResultsIn the central nervous system, neurons, glial cells, immune cells, and tumor cells can transfer mitochondria to each other. Meanwhile, there are many types of mitochondrial transfer, including tunneling nanotubes, extracellular vesicles, receptor cell endocytosis, gap junction channels, and intercellular contact. A variety of stress signals, such as the release of damaged mitochondria, mitochondrial DNA, or other mitochondrial products and the elevation of reactive oxygen species, can trigger the transfer of mitochondria from donor cells to recipient cells. Concurrently, a variety of molecular pathways and related inhibitors can affect mitochondrial intercellular transfer. ConclusionThis study reviews the phenomenon of intercellular mitochondrial transfer in the central nervous system and summarizes the corresponding transfer pathways. Finally, we propose targeted pathways and treatment methods that may be used to regulate mitochondrial transfer for the treatment of related diseases.

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