期刊
BRAIN RESEARCH
卷 1111, 期 -, 页码 222-226出版社
ELSEVIER
DOI: 10.1016/j.brainres.2006.06.041
关键词
Alzheimer's disease; proteolysis; ApoE
资金
- NIA NIH HHS [R01-AG21084, R01-AG20570] Funding Source: Medline
- NINDS NIH HHS [R01-NS48422, R01-NS40529, P50-NS10828] Funding Source: Medline
Matrix metalloproteinase-9 (MMP-9) may play a role in the inflammatory glial response during Alzheimer's disease (AD). Astrocytes can degrade beta-amyloid (A beta) and extracellular proteolysis via MMP-9 may be involved. Because Apolipoprotein E (APOE) genotype is an important factor for AD, we ask whether various apoE isoforms can influence A beta-induced MMP-9 responses in primary rat astrocytes. Our data show that apoE4 significantly dampens A beta-induced MMP-9 levels, possibly by downregulating the Rho-Rho kinase (ROCK) pathway. Reduction of astrocytic MMP-9 by apoE4 may affect A beta clearance and promote A beta deposition in AD. (c) 2006 Elsevier B.V. All rights reserved.
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