Mayo Clinic researchers have now shown that a drug that inhibits the function of the protein Hsp90 reduces brain levels in mice of the protein tau, the abnormal accumulation of which has been implicated in the pathogenesis of Alzheimer’s disease (AD). The study appears online on February 15 in advance of publication in the March print issue of the Journal of Clinical Investigation.
A hallmark of AD is the abnormal accumulation of phosphorylated tau (p-tau) proteins resulting in the formation of neurofibrillary tangles, which impair the function of brain axons. Enhancing the removal of these p-tau proteins may therefore be a relevant therapeutic strategy. In the current study, Leonard Petrucelli and colleagues from the Mayo Clinic showed that a complex of two proteins, CHIP and Hsp90 (which are involved in protein refolding and degradation), plays a role in alleviating p-tau accumulation in mice and cultured human cells. They went on to show that administration of an Hsp90 inhibitor, EC102, to mice overexpressing human tau caused a significant reduction in p-tau levels.
The findings point to a pivotal role for Hsp90 in aberrant tau degradation and potentially in tau refolding. Unlike many drugs, EC102 is able to cross the blood-brain barrier, making it a highly promising therapeutic candidate for AD and other conditions in which tau accumulates in abnormally high levels in the brain.
TITLE: The high-affinity HSP90-CHIP complex recognizes and selectively degrades phosphorylated tau client proteins
AUTHOR CONTACT:
Leonard Petrucelli
Mayo Clinic College of Medicine, Jacksonville, Florida, USA.
Phone : (904) 953-2855; Fax: (904) 953-7370; E-mail: petrucelli.leonard@mayo.edu
View the PDF of this article at: https://www.the-jci.org/article.php?id=29715
Journal
The Journal of Infectious Diseases