EXCEED THE SPACE PROVIDED. Monocyte/macrophages (M/M_)) play a key role in the neuropathogenesis of HIV-associated dementia (HAD) through inflammatory responses that cause neuronal injury and apoptosis. Prior to the advent of highly active anti-retroviral therapies (HAART), HAD was an acute neurodegenerative disease that was aggressive and terminal. Fortunately, where treatment with HAART is available, there has been a decrease in the incidence and severity of HAD. However, no data is available to indicate that HAART protects the brain or reverses the neuropathology associated with HIV infection. In fact, studies from our laboratory suggest that HAD- associated peripheral markers and M/Mqb-derived factors are diminished but still present. It is possible that HAD has become a chronic neurodegenerative disease. It is the overall hypothesis of this proposal that HAD may manifest a peripheral profile years before clinical dementia.
Our Specific Aims are: 1) To develop a M/M_ expression profile from individuals with HAD using cDNA microarrays and proteomics technology and 2) To identify unique proteins secreted from M/M_ supernatants of patients with HAD using proteomics technology. To identify signaling pathways and structural/functional protein changes associated with supernatant-treated human brain aggregates using cDNA microarrays and proteomics. To determine whether or not APOE genotype affects these neural cell changes. Since neurodegeneration related to HAD may occur years before becoming clinically evident, it is important to identify individuals early in the disease process to improve the response to therapeutic intervention. Results from these studies will not only profile individuals at risk for dementia but also better elucidate the mechanisms for the risk. >ERFORMANCE SITE(S) (organization, city, state) qorthern California Institute for Research and Education (NCIRE), San Francisco, CA Department of Veterans Affairs Medical Center, San Francisco, CA KEY PERSONNEL ========================================Section End===========================================

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21MH064406-03
Application #
6819272
Study Section
AIDS and Related Research 8 (AARR)
Program Officer
Joseph, Jeymohan
Project Start
2002-12-01
Project End
2006-05-31
Budget Start
2004-12-01
Budget End
2006-05-31
Support Year
3
Fiscal Year
2005
Total Cost
$123,750
Indirect Cost
Name
Northern California Institute Research & Education
Department
Type
DUNS #
613338789
City
San Francisco
State
CA
Country
United States
Zip Code
94121
Sun, Bing; Rempel, Hans C; Pulliam, Lynn (2004) Loss of macrophage-secreted lysozyme in HIV-1-associated dementia detected by SELDI-TOF mass spectrometry. AIDS 18:1009-12
Pulliam, Lynn; Sun, Bing; Rempel, Hans (2004) Invasive chronic inflammatory monocyte phenotype in subjects with high HIV-1 viral load. J Neuroimmunol 157:93-8