Tau blocks traffic of organelles, neurofilaments, and APP vesicles in neurons and enhances oxidative stress
Max Planck Unit for Structural Molecular Biology
Abstract
We studied the effect of microtubule-associated tau protein on trafficking of vesicles and organelles in primary cortical neurons, retinal ganglion cells, and neuroblastoma cells. Tau inhibits kinesin-dependent transport of peroxisomes, neurofilaments, and Golgi-derived vesicles into neurites. Loss of peroxisomes makes cells vulnerable to oxidative stress and leads to degeneration. In particular, tau inhibits transport of amyloid precursor protein (APP) into axons and dendrites, causing its accumulation in the cell body. APP tagged with yellow fluorescent protein and transfected by adenovirus associates with vesicles moving rapidly forward in the axon (approximately 80%) and slowly back (approximately 20%).…
Citation impact
- FWCI
- 20.27
- Percentile
- 100%
- References
- 73
Authors
5- KSKarsten StamerCorresponding
Max Planck Unit for Structural Molecular Biology
- RVRobert Vogel
Max Planck Unit for Structural Molecular Biology
- ETEdda Thies
Max Planck Unit for Structural Molecular Biology
- EMEckhard Mandelkow�
Max Planck Unit for Structural Molecular Biology
- EMEckhard Mandelkow�
Max Planck Unit for Structural Molecular Biology
Topics & keywords
- Cell biology
- Biology
- Golgi apparatus
- Neurite
- Neurofilament
- Kinesin
- Axon
- Microtubule