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PMID: 2106906 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Differential expression of amyloid precursor protein mRNAs in cases of Alzheimer's disease and in aged nonhuman primates.

Neuron ·Vol. 4 ·No. 1 ·1990-01-00 ·Pages 97-104

Koo EH, Sisodia SS, Cork LC, Unterbeck A, Bayney RM, Price DL

Abstract

Senile plaques are a characteristic feature in brains of individuals with Alzheimer's disease (AD) and aged monkeys. The principal component of amyloid in senile plaques is beta/A4, a peptide derived from a larger amyloid precursor protein (APP). To date, several alternatively spliced APP transcripts have been described. The relationship between levels of these APP mRNAs and amyloid deposition is unclear. In this study, we directly measured the relative levels of APP transcripts that lack the protease inhibitor domain (APP-695) and transcripts that encode the inhibitor sequences (APP-751/770). Our results indicate that the expression of APP mRNAs is not selectively altered in AD cortex. Moreover, the differential expression of APP transcripts is not correlated with the deposition of amyloid in cases of AD and aged monkeys. These findings suggest that other factors, not directly related to the relative expression of APP mRNAs, may contribute to amyloidogenesis in the brain.

MeSH Terms
Aging/genetics Alzheimer Disease/genetics Amyloid/analysis Amyloid beta-Protein Precursor Animals Brain Chemistry Humans Primates Protein Precursors/analysis RNA, Messenger/analysis
Chemicals
Amyloid Amyloid beta-Protein Precursor Protein Precursors RNA, Messenger
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Koo E H
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205-2181.
Sisodia S S
Cork L C
Unterbeck A
Bayney R M
Price D L
Article Info
Journal
Neuron
Abbr.
Neuron
ISSN
0896-6273
Published
1990-01-00
Pages
97-104
Language
English
Region
United States
NLM ID
8809320
Subset
IM
Grants
NIA NIH HHS · AG 03359 · United States
NIA NIH HHS · AG 05146 · United States
NINDS NIH HHS · NS 20471 · United States
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