Emergence of directional bias in tau deposition from axonal transport dynamics
Defects in axonal transport may partly underpin the differences between the observed pathophysiology of Alzheimers disease (AD) and that of other non-amyloidogenic tauopathies. Particularly, pathological tau variants may have molecular properties that dysregulate motor proteins responsible for the anterograde-directed transport of tau in a disease-specific fashion. Here we develop the first computational model of tau-modified axonal transport that produces directional biases in the spread of tau pathology. We simulated the spatiotemporal profiles of soluble and insoluble tau species in a multicompartment, two-neuron system using biologically plausible parameters and time scales. Changes in the balance of tau transport feedback parameters can elicit anterograde and retrograde biases in the distributions of soluble and insoluble tau between compartments in the system. Aggregation and fragmentation parameters can also perturb this balance, suggesting a complex interplay between these distinct molecular processes. Critically, we show that the model faithfully recreates the characteristic network spread biases in both AD-like and non-AD-like mouse tauopathy models. Tau transport feedback may therefore help link microscopic differences in tau conformational states and the resulting variety in clinical presentations. Author SummaryThe misfolding and spread of the axonal protein tau is a hallmark of the pathology of many neurodegenerative disorders, including Alzheimers disease and frontotemporal lobar dementia. How tau misfolding causes disorders with distinct neuropathology and clinical presentations is the subject of ongoing research. Although current evidence suggests that the specific conformations tau adopts affect where it spreads throughout the brain, a mechanistic explanation has remained elusive. Here we propose that the conformer-specific dysregulation of axonal transport can lead to directionally biased spread, and we employ a mathematical model to explore how tau spreads between neurons in the context of this transport feedback mechanism. We find that conformation-specific feedback is flexible enough to explain bias in either direction and thoroughly explore how this bias emerges as a function of the models key parameters. Further, the model reproduces the temporal evolution of directionality observed in two classes of in vivo tauopathy models, demonstrating that transport feedback is sufficient to explain differential tau spread as a function of conformation.