Differential effect of three-repeat and four-repeat tau on mitochondrial axonal transport |
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Authors: | Will Stoothoff&dagger ,Phillip B. Jones,Tara L. Spires-Jones,Daniel Joyner,Ekta Chhabra,Kathryn Bercury&Dagger ,Zhanyun Fan,Hong Xie,Brian Bacskai,Jon Edd§ ,Daniel Irimia§ , Bradley T. Hyman |
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Affiliation: | MassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital, Harvard Medical School, Charlestown, Massachusetts, USA; University of Massachusetts Medical School, Worcester, Massachusetts, USA; University of Colorado Health Science Center, Denver, Colorado, USA; BioMEMS Resource Center, Center for Engineering in Medicine and Surgical Services, Massachusetts General Hospital, Shriners Hospital for Children, and Harvard Medical School, Boston, Massachusetts, USA |
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Abstract: | Tau protein is present in six different splice forms in the human brain and interacts with microtubules via either 3 or 4 microtubule binding repeats. An increased ratio of 3 repeat to 4 repeat isoforms is associated with neurodegeneration in inherited forms of frontotemporal dementia. Tau over-expression diminishes axonal transport in several systems, but differential effects of 3 repeat and 4 repeat isoforms have not been studied. We examined the effects of tau on mitochondrial transport and found that both 3 repeat and 4 repeat tau change normal mitochondrial distribution within the cell body and reduce mitochondrial localization to axons; 4 repeat tau has a greater effect than 3 repeat tau. Further, we observed that the 3 repeat and 4 repeat tau cause different alterations in retrograde and anterograde transport dynamics with 3 repeat tau having a slightly stronger effect on axon transport dynamics. Our results indicate that tau-induced changes in axonal transport may be an underlying theme in neurodegenerative diseases associated with isoform specific changes in tau's interaction with microtubules. |
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Keywords: | Alzheimer's disease axonal transport mitochondria tau tauopathy |
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