期刊
BRAIN PATHOLOGY
卷 31, 期 1, 页码 103-119出版社
WILEY
DOI: 10.1111/bpa.12883
关键词
neurodegeneration; neuroinflammation; PKR; Tau; tauopathies
资金
- Lundbeck Foundation [R248-2016-2518, R223-2015-4222]
- Laboratory for Molecular Infection Medicine Sweden (MIMS)
- Aarhus University
The abnormal phosphorylation of tau protein, mediated by PKR kinase, plays a crucial role in the pathogenesis of tauopathies like Alzheimer's disease. PKR can directly phosphorylate tau at specific residues, leading to its displacement from microtubules and dysregulation of gene expression, particularly during acute brain inflammation.
Deposition of extensively hyperphosphorylated tau in specific brain cells is a clear pathological hallmark in Alzheimer's disease and a number of other neurodegenerative disorders, collectively termed the tauopathies. Furthermore, hyperphosphorylation of tau prevents it from fulfilling its physiological role as a microtubule-stabilizing protein and leaves it increasingly vulnerable to self-assembly, suggestive of a central underlying role of hyperphosphorylation as a contributing factor in the etiology of these diseases. Viain vitrophosphorylation and regulation of kinase activity within cells and acute brain tissue, we reveal that the inflammation associated kinase, protein kinase R (PKR), directly phosphorylates numerous abnormal and disease-modifying residues within tau including Thr181, Ser199/202, Thr231, Ser262, Ser396, Ser404 and Ser409. Similar to disease processes, these PKR-mediated phosphorylations actively displace tau from microtubules in cells. In addition, PKR overexpression and knockdown, respectively, increase and decrease tau protein and mRNA levels in cells. This regulation occurs independent of noncoding transcriptional elements, suggesting an underlying mechanism involving intra-exonic regulation of the tau-encoding microtubule-associated protein tau (MAPT) gene. Finally, acute encephalopathy in wild type mice, induced by intracranial Langat virus infection, results in robust inflammation and PKR upregulation accompanied by abnormally phosphorylated full-length- and truncated tau. These findings indicate that PKR, independent of other kinases and upon acute brain inflammation, is capable of triggering pathological modulation of tau, which, in turn, might form the initial pathologic seed in several tauopathies such as Alzheimer's disease and Chronic traumatic encephalopathy where inflammation is severe.
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