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The Functions, Methods, and Mobility of Mitochondrial Transfer Between Cells

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FRONTIERS IN ONCOLOGY
卷 11, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2021.672781

关键词

mitochondria; transcellular transport; tunneling nanotubes; extracellular vesicles; Cx43 gap junction; Miro; myosin XIX

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资金

  1. Science and Technology Foundation Survey Project of Ministry of Science and Technology of China [2018FY100900, 2018FY10090004]

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Mitochondria are crucial organelles in cells, playing key roles in energy metabolism and apoptosis. Transcellular transfer of mitochondria, facilitated by structures like tunneling nanotubes, extracellular vesicles, and Cx43 gap junctions, is driven by a transport complex. Adapters like mitochondrial Rho small GTPase MIRO and motor proteins like myosin XIX aid in the transcellular transport of mitochondria. This review discusses the roles of these structures in mitochondrial transcellular transfer and their potential for clinical therapies.
Mitochondria are vital organelles in cells, regulating energy metabolism and apoptosis. Mitochondrial transcellular transfer plays a crucial role during physiological and pathological conditions, such as rescuing recipient cells from bioenergetic deficit and tumorigenesis. Studies have shown several structures that conduct transcellular transfer of mitochondria, including tunneling nanotubes (TNTs), extracellular vesicles (EVs), and Cx43 gap junctions (GJs). The intra- and intercellular transfer of mitochondria is driven by a transport complex. Mitochondrial Rho small GTPase (MIRO) may be the adaptor that connects the transport complex with mitochondria, and myosin XIX is the motor protein of the transport complex, which participates in the transcellular transport of mitochondria through TNTs. In this review, the roles of TNTs, EVs, GJs, and related transport complexes in mitochondrial transcellular transfer are discussed in detail, as well as the formation mechanisms of TNTs and EVs. This review provides the basis for the development of potential clinical therapies targeting the structures of mitochondrial transcellular transfer.

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