Article ID Journal Published Year Pages File Type
6271405 Neuroscience 2016 11 Pages PDF
Abstract

•Distribution of aggregated Tau protein is limited by the neural ECM.•Aggregated Tau protein is internalized by cells within one hour.•Internalization of Tau is restricted by the perineuronal nets, a special form of ECM.•Distribution and internalization of Tau is increased in tissue of ECM-knockout mice.

Alzheimer's disease (AD) is a chronic degenerative disorder characterized by fibrillary aggregates of Aß and Tau-protein. Formation and progression of these pathological hallmarks throughout the brain follow a specific spatio-temporal pattern which provides the basis for neuropathological staging. Previously, we could demonstrate that cortical and subcortical neurons are less frequently affected by neurofibrillary degeneration if they are enwrapped by a specialized form of the hyaluronan-based extracellular matrix (ECM), the so called 'perineuronal net' (PN). PNs are composed of large aggregating chondroitin sulfate proteoglycans connected to a hyaluronan backbone, stabilized by link proteins and cross-linked via tenascin-R. Recently, PN-associated neurons were shown to be better protected against iron-induced neurodegeneration compared to neurons without PN, indicating a neuroprotective function. Here, we investigated the role of PNs in distribution and internalization of exogenous Tau-protein by using organotypic slice cultures of wildtype mice as well as mice lacking the ECM-components aggrecan, HAPLN1 or tenascin-R. We could demonstrate that PNs restrict both distribution and internalization of Tau. Accordingly, PN-ensheathed neurons were less frequently affected by Tau-internalization, than neurons without PN.Finally, the PNs as well as their three investigated components were shown to modulate the processes of distribution as well as internalization of Tau.

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Life Sciences Neuroscience Neuroscience (General)
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