Expression and regulation of antiviral protein APOBEC3G in human neuronal cells

• Published in: Journal of neuroimmunology 2009-01, Vol.206 (1), p.14-21
• Main Authors: Wang, Yan-Jian, Wang, Xu, Zhang, Hui, Zhou, Lin, Liu, Shi, Kolson, Dennis L, Song, Li, Ye, Li, Ho, Wen-Zhe
• Format: Article
• Language: English
• Subjects: Allergy and Immunology; APOBEC-3G Deaminase; APOBEC3G; Astrocytes; Brain - cytology; Cell Line, Tumor; Cells, Cultured; Culture Media, Conditioned - pharmacology; Cytidine Deaminase - genetics; Cytidine Deaminase - metabolism; Cytokine; Cytokines - pharmacology; Dose-Response Relationship, Drug; Gene Expression - drug effects; Gene Expression - physiology; Gene Expression Regulation - drug effects; Gene Expression Regulation - physiology; Human immunodeficiency virus 1; Humans; Interferon; Lipopolysaccharides - pharmacology; Macrophages - chemistry; Neuroblastoma; Neurology; Neuron; Neurons - drug effects; Neurons - metabolism; RNA, Messenger - metabolism; RNA, Small Interfering - pharmacology; Time Factors
• ISSN: 0165-5728; 1872-8421
• DOI: 10.1016/j.jneuroim.2008.10.003

Abstract Apolipoprotein B mRNA-editing enzyme, catalytic polypeptide-like 3G (APOBEC3G) has recently been identified as a potent antiviral protein. Here, we examined the expression and regulation of APOBEC3G in human brain tissues and the cells of central nervous system (CNS). Similar to the immune cells, human brain tissue and the CNS cells expressed APOBEC3G at both mRNA and protein levels. The expression of APOBEC3G could be up-regulated in human neuronal cells (NT2-N) and astrocytes (U87-MG) by interferons (IFN-α, β and γ), interleukin-1 (IL-1), and tumor necrosis factor. Other cytokines (IL-4, IL-6 and transforming growth factor beta1) and CC-chemokines (CCL3, 4 and 5), however, had little impact on the expression of APOBEC3G. In addition, pseudotyped HIV-1 infection and cytokine/chemokine-enriched supernatants from lipopolysaccharide-stimulated macrophage cultures induced APOBEC3G expression in NT2-N cells. APOBEC3G expressed in the neuronal cells and astrocytes was biologically functional, as the suppression of APOBEC3G expression by the specific siRNA led to increase of pseudotyped HIV-1 replication in these cells. These findings provide direct and compelling evidence that there is intracellular expression and regulation of functional APOBEC3G in the neuronal cells, which may be one of innate defense mechanisms involved in the neuronal protection in the CNS.