Gap junctions (GJ) are the only channels by which cells can communicate directly with the cytoplasm of neighboring cells. In the nervous system neuronal stem cells, neurons, astrocytes, oligodendrocytes, blood brain barrier cells (endothelial and astrocytes), and under inflammatory conditions, microglia express GJ. The normal function of these channels is to propagate intercellular messengers, such as calcium, nucleotides, IPS, metabolites, and electrical signals that ultimately coordinate tissue homeostasis, proliferation, differentiation, metabolism and cell death. To date little is known about the role that GJ play during the pathogenesis of human nervous system diseases, including HIV-infection. Almost all the data have been obtained in mouse and rat models. Our preliminary data, using human cells, are the first evidence that GJ may actively participate in NeuroAIDS. We propose that they amplify toxic signals generated by HIV-infected astrocytes. Our hypothesis is that HIV infected astrocytes use intercellular communication through gap junctions to spread toxic and inflammatory signals into uninfected cells to compromise their function and viability, leading further to CNS dysfunction. To address this hypothesis three Aims are proposed.
Aim 1 : To determine the mechanisms by which HIV- infection in astrocytes maintain or enhances or expression of GJ.
Aim 2 : To determine the pathophysiological consequences of gap junction communication between HIV-infected astrocytes and uninfected cells.
Aim 3 : To determine the signal (s) that diffuse through gap junctions to alter the function of uninfected cells. The results from these studies should contribute to our understanding of the role of gap junction channels in the development of NeuroAIDS, and may indicate new strategies to control the neurodegeneration often associated with HIV-infection. In addition, this proposal represents an outstanding opportunity for me to be trained in an outstanding environment, in the laboratory of Dr. Joan W. Berman, where studies of NeuroAIDS are ongoing, and at The Albert Einstein College of Medicine.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Scientist Development Award - Research & Training (K01)
Project #
5K01MH076679-04
Application #
7577551
Study Section
Special Emphasis Panel (ZRG1-AARR-H (05))
Program Officer
Joseph, Jeymohan
Project Start
2006-03-03
Project End
2011-02-28
Budget Start
2009-03-01
Budget End
2010-02-28
Support Year
4
Fiscal Year
2009
Total Cost
$131,300
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Pathology
Type
Schools of Medicine
DUNS #
110521739
City
Bronx
State
NY
Country
United States
Zip Code
10461
Mavrianos, John; Berkow, Elizabeth L; Desai, Chirayu et al. (2013) Mitochondrial two-component signaling systems in Candida albicans. Eukaryot Cell 12:913-22
D'Aversa, T G; Eugenin, E A; Lopez, L et al. (2013) Myelin basic protein induces inflammatory mediators from primary human endothelial cells and blood-brain barrier disruption: implications for the pathogenesis of multiple sclerosis. Neuropathol Appl Neurobiol 39:270-83
Qian, X; Hulit, J; Suyama, K et al. (2013) p21CIP1 mediates reciprocal switching between proliferation and invasion during metastasis. Oncogene 32:2292-2303.e7
Chung, S; Yao, J; Suyama, K et al. (2013) N-cadherin regulates mammary tumor cell migration through Akt3 suppression. Oncogene 32:422-30
Megra, Bezawit; Eugenin, Eliseo; Roberts, Toni et al. (2013) Protease resistant protein cellular isoform (PrP(c)) as a biomarker: clues into the pathogenesis of HAND. J Neuroimmune Pharmacol 8:1159-66
Hazleton, Joy E; Berman, Joan W; Eugenin, Eliseo A (2012) Purinergic receptors are required for HIV-1 infection of primary human macrophages. J Immunol 188:4488-95
Eugenin, Eliseo A; Basilio, Daniel; Sáez, Juan C et al. (2012) The role of gap junction channels during physiologic and pathologic conditions of the human central nervous system. J Neuroimmune Pharmacol 7:499-518
Williams, Dionna W; Eugenin, Eliseo A; Calderon, Tina M et al. (2012) Monocyte maturation, HIV susceptibility, and transmigration across the blood brain barrier are critical in HIV neuropathogenesis. J Leukoc Biol 91:401-15
Roberts, Toni K; Eugenin, Eliseo A; Lopez, Lillie et al. (2012) CCL2 disrupts the adherens junction: implications for neuroinflammation. Lab Invest 92:1213-33
Eugenin, E A; King, J E; Hazleton, J E et al. (2011) Differences in NMDA receptor expression during human development determine the response of neurons to HIV-tat-mediated neurotoxicity. Neurotox Res 19:138-48

Showing the most recent 10 out of 24 publications