The physiological link between metabolic rate depression and tau phosphorylation in mammalian hibernation

• Published in: PloS one 2011-01, Vol.6 (1), p.e14530-e14530
• Main Authors: Stieler, Jens T, Bullmann, Torsten, Kohl, Franziska, Tøien, Øivind, Brückner, Martina K, Härtig, Wolfgang, Barnes, Brian M, Arendt, Thomas
• Format: Article
• Language: English
• Subjects: Agglomeration; Alzheimer's disease; Analysis; Animal models; Animals; Arousal; Basal Metabolism; Bears; Black bear; Body Temperature; Brain; Brain - metabolism; Brain research; Cell Biology; Cell Biology/Neuronal and Glial Cell Biology; Cricetinae; Dephosphorylation; Ground squirrels; Hamsters; Hibernation; In vivo methods and tests; Insulin resistance; Kinases; Kinetics; Mammals; Mental depression; Mesocricetus; Metabolic rate; Molecular Biology; Molecular modelling; Nervous system diseases; Neurodegeneration; Neurodegenerative diseases; Neurofibrillary tangles; Neurological diseases; Neurological Disorders/Alzheimer Disease; Neuroscience; Neuroscience/Neuronal and Glial Cell Biology; Pathogenesis; Phosphates; Phosphorylation; Phosphotransferases; Physiological aspects; Physiology; Polar environments; Protein turnover; Reaction kinetics; Regulatory mechanisms (biology); Rodents; Sciuridae; Squirrels; Tau protein; tau Proteins - metabolism; Temperature; Torpor; Ursidae; Ursus americanus
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0014530

Abnormal phosphorylation and aggregation of tau protein are hallmarks of a variety of neurological disorders, including Alzheimer's disease (AD). Increased tau phosphorylation is assumed to represent an early event in pathogenesis and a pivotal aspect for aggregation and formation of neurofibrillary tangles. However, the regulation of tau phosphorylation in vivo and the causes for its increased stage of phosphorylation in AD are still not well understood, a fact that is primarily based on the lack of adequate animal models. Recently we described the reversible formation of highly phosphorylated tau protein in hibernating European ground squirrels. Hence, mammalian hibernation represents a model system very well suited to study molecular mechanisms of both tau phosphorylation and dephosphorylation under in vivo physiological conditions. Here, we analysed the extent and kinetics of hibernation-state dependent tau phosphorylation in various brain regions of three species of hibernating mammals: arctic ground squirrels, Syrian hamsters and black bears. Overall, tau protein was highly phosphorylated in torpor states and phosphorylation levels decreased after arousal in all species. Differences between brain regions, hibernation-states and phosphosites were observed with respect to degree and kinetics of tau phosphorylation. Furthermore, we tested the phosphate net turnover of tau protein to analyse potential alterations in kinase and/or phosphatase activities during hibernation. Our results demonstrate that the hibernation-state dependent phosphorylation of tau protein is specifically regulated but involves, in addition, passive, temperature driven regulatory mechanisms. By determining the activity-state profile for key enzymes of tau phosphorylation we could identify kinases potentially involved in the differentially regulated, reversible tau phosphorylation that occurs during hibernation. We show that in black bears hibernation is associated with conformational changes of highly phosphorylated tau protein that are typically related to neuropathological alterations. The particular hibernation characteristics of black bears with a continuous torpor period and an only slightly decreased body temperature, therefore, potentially reflects the limitations of this adaptive reaction pattern and, thus, might indicate a transitional state of a physiological process.