Clinical Proteomics | |
Unique and differential protein signatures within the mononuclear cells of HIV-1 and HCV mono-infected and co-infected patients | |
Pooja Jain4  Ramila Philip1  Andrew H Talal2  Punit Shah1  Zacharie Nickens1  Jordana Coelho-dos-Reis4  Martha Ricaurte3  Luis Cubano3  Vivekananda Shetty1  Nawal M Boukli3  | |
[1] Immunotope, Inc., Pennsylvania Biotechnology Center, Doylestown, PA, USA;Center for the Study of Hepatitis C, Weill Cornell Medical College, New York, NY, USA;Universidad Central del Caribe School of Medicine, Biomedical Proteomics Facility Department of Microbiology and Immunology, Bayamon, Puerto Rico;Department of Microbiology and Immunology, and the Drexel Institute for Biotechnology and Virology Research, Drexel University College of Medicine, 3805 Old Easton Road, Doylestown, PA, USA | |
关键词: Proteomics; Pro- and anti-apoptotic fingerprinting; Mass spectrometry; 2D-GE; HIV-1/HCV; HCV; HIV-1; | |
Others : 1026353 DOI : 10.1186/1559-0275-9-11 |
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received in 2011-08-12, accepted in 2012-02-15, 发布年份 2012 | |
【 摘 要 】
Background
Pathogenesis of liver damage in patients with HIV and HCV co-infection is complex and multifactorial. Although global awareness regarding HIV-1/HCV co-infection is increasing little is known about the pathophysiology that mediates the rapid progression to hepatic disease in the co-infected individuals.
Results
In this study, we investigated the proteome profiles of peripheral blood mononuclear cells from HIV-1 mono-, HCV mono-, and HIV-1/HCV co-infected patients. The results of high-resolution 2D gel electrophoresis and PD quest software quantitative analysis revealed that several proteins were differentially expressed in HIV-1, HCV, and HIV-1/HCV co-infection. Liquid chromatography-mass spectrometry and Mascot database matching (LC-MS/MS analysis) successfully identified 29 unique and differentially expressed proteins. These included cytoskeletal proteins (tropomyosin, gelsolin, DYPLSL3, DYPLSL4 and profilin-1), chaperones and co-chaperones (HSP90-beta and stress-induced phosphoprotein), metabolic and pre-apoptotic proteins (guanosine triphosphate [GTP]-binding nuclear protein Ran, the detoxifying enzyme glutathione S-transferase (GST) and Rho GDP-dissociation inhibitor (Rho-GDI), proteins involved in cell prosurvival mechanism, and those involved in matrix synthesis (collagen binding protein 2 [CBP2]). The six most significant and relevant proteins were further validated in a group of mono- and co-infected patients (n = 20) at the transcriptional levels.
Conclusions
The specific pro- and anti- apoptotic protein signatures revealed in this study could facilitate the understanding of apoptotic and protective immune-mediated mechanisms underlying HIV-1 and HCV co-infection and their implications on liver disease progression in co-infected patients.
【 授权许可】
2012 Boukli et al.; licensee BioMed Central Ltd.
【 预 览 】
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