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multiple myeloma (MM)), inflammation and ischemic stroke and is an important therapeutic target

Although DRP1 was once believed not to be involved in MDV synthesis [55], recent studies have indicated that the DRP1 receptors MID49, 51, and MFF recruit DRP1 to membrane protrusions, resulting in membrane fission and the formation of MDVs containing specific components [56]

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However, inadequate metabolism can disturb mitochondrial dysfunction, improper cellular homeostasis, and ROS formation [8, 9]