Because aged nonhuman primates show ?-amyloid (A?) deposition in senile plaques and blood vessels similar to that seen in human aging and AD, C-terminal-specific antibodies to A?40 and A?42 were used to investigate A? peptide length in the brains of 11 aged rhesus monkeys and a 59-year-old chimpanzee. In contrast to AD, where the earliest and most prominent form of A? in senile plaques is A?42 in the monkey, A?40-positive plaques predominated. The ratio of A?40:A?42-positive plaques averaged 2.08 in the monkey, as compared to a mean ratio of 0.37 in 68 human AD subjects (p < 0.001). A?40 was also more prominent in the chimpanzee than in humans. Possible explanations for these findings include species differences in the cleavage of A? from the amyloid precursor protein or in the activity of a putative carboxy peptidase forming A?40 from A?42 in situ.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
3P51RR000165-37S1
Application #
2711873
Study Section
Project Start
Project End
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
37
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Emory University
Department
Type
DUNS #
042250712
City
Atlanta
State
GA
Country
United States
Zip Code
30322
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