Affiliations: [a] Department of Biology, University of Virginia, Charlottesville, VA, USA
| [b] Department of CellBiology, University of Virginia, Charlottesville, VA, USA
| [c] Department of Biomedical Engineering, Universityof Virginia, Charlottesville, VA, USA
| [d] Department of Neuroscience, University ofVirginia, Charlottesville, VA, USA
Correspondence:
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Correspondence to: George S. Bloom, Department of Biology, University of Virginia, PO Box 400328, Charlottesville, VA, 22904-4328, USA. Tel.: +1 434 243 3543; E-mail: [email protected].
Abstract: Aggregates composed of the microtubule associated protein, tau, are a hallmark of Alzheimer’s disease and non-Alzheimer’s tauopathies. Extracellular tau can induce the accumulation and aggregation of intracellular tau, and tau pathology can be transmitted along neural networks over time. There are six splice variants of central nervous system tau, and various oligomeric and fibrillar forms are associated with neurodegeneration in vivo. The particular extracellular forms of tau capable of transferring tau pathology from neuron to neuron remain ill defined, however, as do the consequences of intracellular tau aggregation on neuronal physiology. The present study was undertaken to compare the effects of extracellular tau monomers, oligomers, and filaments comprising various tau isoforms on the behavior of cultured neurons. We found that 2N4R or 2N3R tau oligomers provoked aggregation of endogenous intracellular tau much more effectively than monomers or fibrils, or of oligomers made from other tau isoforms, and that a mixture of all six isoforms most potently provoked intracellular tau accumulation. These effects were associated with invasion of tau into the somatodendritic compartment. Finally, we observed that 2N4R oligomers perturbed fast axonal transport of membranous organelles along microtubules. Intracellular tau accumulation was often accompanied by increases in the run length, run time and instantaneous velocity of membranous cargo. This work indicates that extracellular tau oligomers can disrupt normal neuronal homeostasis by triggering axonal tau accumulation and loss of the polarized distribution of tau, and by impairing fast axonal transport.
