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Gene expression changes consistent with neuroAIDS and impaired working memory in HIV-1 transgenic rats

Title: Gene expression changes consistent with neuroAIDS and impaired working memory in HIV-1 transgenic rats
Authors: Repunte-Canonigo, Vez; Lefebvre, Celine; George, Olivier; Kawamura, Tomoya; Morales, Marisela; Koob, George F; Califano, Andrea; Masliah, Eliezer; Sanna, Pietro Paolo
Source: Molecular Neurodegeneration, vol 9, iss 1
Publisher Information: eScholarship, University of California
Publication Year: 2014
Collection: University of California: eScholarship
Subject Terms: 3207 Medical Microbiology (for-2020); 32 Biomedical and Clinical Sciences (for-2020); 3204 Immunology (for-2020); Sexually Transmitted Infections (rcdc); Infectious Diseases (rcdc); Aging (rcdc); Neurosciences (rcdc); Neurodegenerative (rcdc); Genetics (rcdc); Biotechnology (rcdc); Brain Disorders (rcdc); HIV/AIDS (rcdc); 2.1 Biological and endogenous factors (hrcs-rac); 5.1 Pharmaceuticals (hrcs-rac); Neurological (hrcs-hc); AIDS Dementia Complex (mesh); Animals (mesh); Disease Models; Animal (mesh); HIV Infections (mesh); HIV-1 (mesh); Hippocampus (mesh); Immunohistochemistry (mesh); Memory; Short-Term (mesh); Oligonucleotide Array Sequence Analysis (mesh); Rats (mesh); Rats; Sprague-Dawley (mesh); Transgenic (mesh)
Description: BackgroundA thorough investigation of the neurobiology of HIV-induced neuronal dysfunction and its evolving phenotype in the setting of viral suppression has been limited by the lack of validated small animal models to probe the effects of concomitant low level expression of multiple HIV-1 products in disease-relevant cells in the CNS.ResultsWe report the results of gene expression profiling of the hippocampus of HIV-1 Tg rats, a rodent model of HIV infection in which multiple HIV-1 proteins are expressed under the control of the viral LTR promoter in disease-relevant cells including microglia and astrocytes. The Gene Set Enrichment Analysis (GSEA) algorithm was used for pathway analysis. Gene expression changes observed are consistent with astrogliosis and microgliosis and include evidence of inflammation and cell proliferation. Among the genes with increased expression in HIV-1 Tg rats was the interferon stimulated gene 15 (ISG-15), which was previously shown to be increased in the cerebrospinal fluid (CSF) of HIV patients and to correlate with neuropsychological impairment and neuropathology, and prostaglandin D2 (PGD2) synthase (Ptgds), which has been associated with immune activation and the induction of astrogliosis and microgliosis. GSEA-based pathway analysis highlighted a broad dysregulation of genes involved in neuronal trophism and neurodegenerative disorders. Among the latter are genesets associated with Huntington’s disease, Parkinson’s disease, mitochondrial, peroxisome function, and synaptic trophism and plasticity, such as IGF, ErbB and netrin signaling and the PI3K signal transduction pathway, a mediator of neural plasticity and of a vast array of trophic signals. Additionally, gene expression analyses also show altered lipid metabolism and peroxisomes dysfunction. Supporting the functional significance of these gene expression alterations, HIV-1 Tg rats showed working memory impairments in spontaneous alternation behavior in the T-Maze, a paradigm sensitive to prefrontal cortex and hippocampal ...
Document Type: article in journal/newspaper
File Description: application/pdf
Language: unknown
Relation: qt10v9s846; https://escholarship.org/uc/item/10v9s846; https://escholarship.org/content/qt10v9s846/qt10v9s846.pdf
DOI: 10.1186/1750-1326-9-26
Availability: https://escholarship.org/uc/item/10v9s846; https://escholarship.org/content/qt10v9s846/qt10v9s846.pdf; https://doi.org/10.1186/1750-1326-9-26
Rights: CC-BY
Accession Number: edsbas.95DA794D
Database: BASE