
Mitochondrial morphology is dynamically regulated by the formation of small fragmented units or interconnected mitochondrial networks, and this dynamic morphological change is a pivotal process in normal mitochondrial function. In the present study, we identified a novel regulator responsible for the regulation of mitochondrial dynamics. An assay using CHANG liver cells stably expressing mitochondrial-targeted yellow fluorescent protein (mtYFP) and a group of siRNAs revealed that T-cell intracellular antigen protein-1 (TIA-1) affects mitochondrial morphology by enhancing mitochondrial fission. The function of TIA-1 in mitochondrial dynamics was investigated through various biological approaches and expression analysis in human specimen. Downregulation of TIA-1-enhanced mitochondrial elongation, whereas ectopic expression of TIA-1 resulted in mitochondria fragmentation. In addition, TIA-1 increased mitochondrial activity, including the rate of ATP synthesis and oxygen consumption. Further, we identified mitochondrial fission factor (MFF) as a direct target of TIA-1, and showed that TIA-1 promotes mitochondrial fragmentation by enhancing MFF translation. TIA-1 null cells had a decreased level of MFF and less mitochondrial Drp1, a critical factor for mitochondrial fragmentation, thereby enhancing mitochondrial elongation. Taken together, our results indicate that TIA-1 is a novel factor that facilitates mitochondrial dynamics by enhancing MFF expression and contributes to mitochondrial dysfunction.
Dynamins, Membrane Proteins, Cell Line, GTP Phosphohydrolases, Mitochondria, Mitochondrial Proteins, Luminescent Proteins, Mice, MicroRNAs, Adenosine Triphosphate, Oxygen Consumption, Bacterial Proteins, Microscopy, Fluorescence, Animals, Humans, RNA Interference, RNA, Messenger, 3' Untranslated Regions, Microtubule-Associated Proteins, Plasmids
Dynamins, Membrane Proteins, Cell Line, GTP Phosphohydrolases, Mitochondria, Mitochondrial Proteins, Luminescent Proteins, Mice, MicroRNAs, Adenosine Triphosphate, Oxygen Consumption, Bacterial Proteins, Microscopy, Fluorescence, Animals, Humans, RNA Interference, RNA, Messenger, 3' Untranslated Regions, Microtubule-Associated Proteins, Plasmids
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