Microtubule dynamics and the neurodegenerative triad of Alzheimer's disease: The hidden connection

Autor(en): Brandt, Roland 
Bakota, Lidia
Stichwörter: A-BETA; ABNORMAL PHOSPHORYLATION; AMYLOID-BETA TOXICITY; AXONAL-TRANSPORT; Biochemistry & Molecular Biology; cytoskeleton; D-ASPARTATE RECEPTORS; DENDRITIC SPINE ALTERATIONS; dendritic spines; microtubule dynamics; Neurosciences; Neurosciences & Neurology; PAIRED HELICAL FILAMENTS; PROTEIN-TAU TAU; STABILIZING AGENT; tau protein; TRANSGENIC MOUSE MODEL
Erscheinungsdatum: 2017
Herausgeber: WILEY
Journal: JOURNAL OF NEUROCHEMISTRY
Volumen: 143
Ausgabe: 4, SI
Startseite: 409
Seitenende: 417
Zusammenfassung: 
Alzheimer's disease (AD) is the most common neurodegenerative disorder and is, on a histopathological level, characterized by the presence of extracellular amyloid plaques composed of the protein fragment A, and intracellular neurofibrillary tangles, which contain the microtubule-associated protein tau in a hyperphosphorylated state. In AD defects in microtubule (MT) assembly and organization have also been reported; however, it is unclear whether MT abnormalities have a causal and early role in the disease process or represent a common end point downstream of the neurodegenerative cascade. Recent evidence indicates that microtubule-stabilizing drugs prevent axonopathy in animal models of tauopathies and reverse A-induced loss of synaptic connectivity in an exvivo model of amyloidosis. This could suggest that MT dysfunction connects some of the degenerative events and provides a useful target to simultaneously prevent several neurodegenerative processes in AD. Here, we describe how changes in the structure and dynamics of MTs are involved in the different aspects of the neurodegenerative triad of AD. We discuss evidence that MTs are affected both by tau-dependent and tau-independent mechanisms but appear to be regulated in a distinct way in different neuronal compartments. We argue that modulation of MT dynamics could be of potential benefit but needs to be precisely controlled in a cell and compartment-specific manner to avoid harmful side effects.
ISSN: 00223042
DOI: 10.1111/jnc.14011

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