| Literature DB >> 19686388 |
Will Stoothoff1, Phillip B Jones, Tara L Spires-Jones, Daniel Joyner, Ekta Chhabra, Kathryn Bercury, Zhanyun Fan, Hong Xie, Brian Bacskai, Jon Edd, Daniel Irimia, Bradley T Hyman.
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.Entities:
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Year: 2009 PMID: 19686388 PMCID: PMC2831412 DOI: 10.1111/j.1471-4159.2009.06316.x
Source DB: PubMed Journal: J Neurochem ISSN: 0022-3042 Impact factor: 5.372