PT  - JOURNAL ARTICLE
AU  - Hyang-Sook Hoe
AU  - Matthew J. Cooper
AU  - Mark P. Burns
AU  - Patrick A. Lewis
AU  - Marcel van der Brug
AU  - Geetanjali Chakraborty
AU  - Casandra M. Cartagena
AU  - Daniel T. S. Pak
AU  - Mark R. Cookson
AU  - G. William Rebeck
TI  - The Metalloprotease Inhibitor TIMP-3 Regulates Amyloid Precursor Protein and Apolipoprotein E Receptor Proteolysis
AID  - 10.1523/JNEUROSCI.3135-07.2007
DP  - 2007 Oct 03
TA  - The Journal of Neuroscience
PG  - 10895--10905
VI  - 27
IP  - 40
4099  - http://www.jneurosci.org/content/27/40/10895.short
4100  - http://www.jneurosci.org/content/27/40/10895.full
SO  - J. Neurosci.2007 Oct 03; 27
AB  - Cellular cholesterol levels alter the processing of the amyloid precursor protein (APP) to produce Aβ. Activation of liver X receptors (LXRs), one cellular mechanism to regulate cholesterol homeostasis, has been found to alter Aβ levels in vitro and in vivo. To identify genes regulated by LXR, we treated human neuroblastoma cells with an LXR agonist (TO-901317) and examined gene expression by microarray. As expected, TO-901317 upregulated several cholesterol metabolism genes, but it also decreased expression of a metalloprotease inhibitor, TIMP-3. We confirmed this finding using real-time PCR and by measuring TIMP-3 protein in glia, SY5Y cells, and COS7 cells. TIMP-3 is a member of a family of metalloproteinase inhibitors and blocks A disintegrin and metalloproteinase-10 (ADAM-10) and ADAM-17, two APP α-secretases. We found that TIMP-3 inhibited α-secretase cleavage of APP and an apolipoprotein E (apoE) receptor, ApoER2. TIMP-3 decreased surface levels of ADAM-10, APP, and ApoER2. These changes were accompanied by increased APP β-C-terminal fragment and Aβ production. These data suggest that TIMP-3 preferentially routes APP and ApoER2 away from the cell surface and α-secretase cleavage and encourages endocytosis and β-secretase cleavage. In vivo, TO-901317 decreased brain TIMP-3 levels. TIMP-3 protein levels were increased in human Alzheimer's disease (AD) brain and in APP transgenic mice, suggesting that increased levels of TIMP-3 in AD may contribute to higher levels of Aβ.