Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2004;23(3):189-204.
doi: 10.1385/JMN:23:3:189.

Apolipoprotein E: diversity of cellular origins, structural and biophysical properties, and effects in Alzheimer's disease

Affiliations
Review

Apolipoprotein E: diversity of cellular origins, structural and biophysical properties, and effects in Alzheimer's disease

Yadong Huang et al. J Mol Neurosci. 2004.

Abstract

Apolipoprotein E4 (apoE4) is a major risk factor for Alzheimer's disease (AD). Several hypotheses have been proposed to explain the association of the APOE epsilon4 allele with AD; however, the mechanisms underlying this association are largely unknown. Initially, apoE was thought to be synthesized primarily by astrocytes but not by neurons in the brain. However, subsequent studies have demonstrated that central nervous system neurons also express apoE under diverse physiological and pathological conditions. Detailed studies of the structure and biophysical properties of apoE isoforms have demonstrated unique properties distinguishing apoE4 from apoE3. Because the structural and biophysical properties of a protein determine how it functions under normal and abnormal conditions, apoE4, with its multiple cellular origins and multiple structural and biophysical properties, might contribute to the pathology of AD through several different mechanisms. Some of these mechanisms might be suitable targets for the development of new treatments for AD.

PubMed Disclaimer

References

    1. JAMA. 1997 Oct 22-29;278(16):1349-56 - PubMed
    1. Eur J Neurosci. 2001 Jul;14(2):256-66 - PubMed
    1. Neurosci Lett. 1998 Apr 24;246(2):65-8 - PubMed
    1. Proc Natl Acad Sci U S A. 1993 Sep 1;90(17):8098-102 - PubMed
    1. J Biol Chem. 1981 Sep 10;256(17):9077-83 - PubMed

Publication types

LinkOut - more resources