Core A: The Neuropathology and Cell Culture Core The Neuropathology and Cell Culture Core is the scientific core of this Program Project Grant (PPG). The central role of this Core is to assist the overall objectives of the three research projects within the PPG to determine the different molecular pathways involved in the development of HIV encephalitis in AIDS patients. The Neuropathology and Cell Culture Core will assist the participants of the Program Project by providing surgical and autopsy brain tissue material from HIV-1 infected patients diagnosed with HIV encephalitis, as well as brains from HIV-1 infected individuals with no CNS involvement and normal control brains. In close collaboration with Projects 1, 2 and 3, we will perform immunohistochemical analysis, including double labeling, of viral proteins, cellular markers, and the different downstream molecules of the Rho/Rac pathway and their association with Pur-a (Project 1), the TNFa and Ras pathway and its association with the IGF- 1/IRS pathway (Project 2), and the HIF-1 pathway and its association with Vpr (Project 3). The Neuropathology and Cell Culture Core will also provide highly purified cultures of human fetal microglia, astrocytes, and neurons on demand. Primary cultures of neurons will be prepared from rat and mouse hippocampus for the proposed studies. Established cell lines, such as PC12 will be maintained, cultured, and distributed to the projects. Also, Conditioned Media from HIV-1 infected cells will be prepared for use by the individual projects. Finally, the Core will provide cultures of neurospheres differentiated into different cellular phenotypes, including neurons, oligodendrocytes and astrocytes. The proposed experiments will aid Projects 1, 2 and 3 to decipher the molecular pathways involved in the pathogenesis of HIV encephalitis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
5P01NS043980-09
Application #
8286325
Study Section
National Institute of Neurological Disorders and Stroke Initial Review Group (NSD)
Project Start
Project End
Budget Start
2011-07-01
Budget End
2012-06-30
Support Year
9
Fiscal Year
2011
Total Cost
$182,544
Indirect Cost
Name
Temple University
Department
Type
DUNS #
057123192
City
Philadelphia
State
PA
Country
United States
Zip Code
19122
Sen, Satarupa; Kaminiski, Rafal; Deshmane, Satish et al. (2015) Role of hexokinase-1 in the survival of HIV-1-infected macrophages. Cell Cycle 14:980-9
Wang, Jin Ying; Darbinyan, Armine; White, Martyn K et al. (2014) Involvement of IRS-1 interaction with ADAM10 in the regulation of neurite extension. J Cell Physiol 229:1039-46
Darbinian, Nune; Khalili, Kamel; Amini, Shohreh (2014) Neuroprotective activity of pDING in response to HIV-1 Tat. J Cell Physiol 229:153-61
Wollebo, Hassen S; Woldemichaele, Baheru; White, Martyn K (2013) Lentiviral transduction of neuronal cells. Methods Mol Biol 1078:141-6
Johnson, Edward M; Daniel, Dianne C; Gordon, Jennifer (2013) The pur protein family: genetic and structural features in development and disease. J Cell Physiol 228:930-7
Mishra, Mamata; Del Valle, Luis; Otte, Jessica et al. (2013) Pur-alpha regulates RhoA developmental expression and downstream signaling. J Cell Physiol 228:65-72
Sachdeva, Rakhee; Darbinian, Nune; Khalili, Kamel et al. (2013) DING proteins from phylogenetically different species share high degrees of sequence and structure homology and block transcription of HIV-1 LTR promoter. PLoS One 8:e69623
Bookland, Markus J; Darbinian, Nune; Weaver, Michael et al. (2012) Growth inhibition of malignant glioblastoma by DING protein. J Neurooncol 107:247-56
Darbinian, Nune; Gomberg, Rebeccah; Mullen, Loriann et al. (2011) Suppression of HIV-1 transcriptional elongation by a DING phosphatase. J Cell Biochem 112:225-32
Wilk, Anna; Urbanska, Katarzyna; Yang, Shuo et al. (2011) Insulin-like growth factor-I-forkhead box O transcription factor 3a counteracts high glucose/tumor necrosis factor-?-mediated neuronal damage: implications for human immunodeficiency virus encephalitis. J Neurosci Res 89:183-98

Showing the most recent 10 out of 23 publications