Aluminum inhibits proteolytic degradation of amyloid beta peptide by cathepsin D: a potential link between aluminum accumulation and neuritic plaque deposition.

Abstract:

:Neuritic plaques are the key pathological feature of Alzheimer's disease, and amyloid beta (Abeta) peptides are major component of these plaques. In this study, we demonstrated the influence of aluminum (Al) on the Abeta peptide degradation by cathepsin D. Al did not directly affect the cathepsin D activity using small synthetic substrate. However, when Abeta peptides were used as substrate, the apparent inhibitory effect of Al on cathepsin D activity was observed. This inhibitory effect disappeared by treatment of desferrioxamine. These results indicate that Al has the potential to interact and disrupt Abeta peptide catabolism via the inhibition of proteolytic degradation.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Sakamoto T,Saito H,Ishii K,Takahashi H,Tanabe S,Ogasawara Y

doi

10.1016/j.febslet.2006.10.075

subject

Has Abstract

pub_date

2006-12-11 00:00:00

pages

6543-9

issue

28-29

eissn

0014-5793

issn

1873-3468

pii

S0014-5793(06)01308-1

journal_volume

580

pub_type

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