BK virus large T and VP-1 expression in infected human renal allografts
| Autor: | Stefan Schaub, Norbert H. Seemayer, Fred Gudat, Hans H. Hirsch, Michael J. Mihatsch, Christian A. Seemayer, Ursula Dürmüller |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2017 |
| Předmět: |
Adult
Necrosis viruses Caspase 3 Apoptosis Cell morphology medicine.disease_cause Virus Editorial Reviews medicine Humans Antigens Viral Tumor Aged Viral Structural Proteins Transplantation Polyomavirus Infections biology BK virus nephropathy Cell cycle renal transplantation Middle Aged Virology Kidney Transplantation BK virus Tumor Virus Infections Ki-67 Antigen Proto-Oncogene Proteins c-bcl-2 Nephrology BK Virus Host-Pathogen Interactions biology.protein Keratins Female Kidney Diseases Antibody medicine.symptom Tumor Suppressor Protein p53 |
| Zdroj: | Nephrology Dialysis Transplantation |
| Popis: | OBJECTIVE: We investigated the expression of early and late phase BK virus (BKV) proteins and their interactions with host cell proteins in renal allografts, with ongoing polyomavirus associated nephropathy (PVAN), and correlated this with the nuclear and cell morphology. METHODS: Frozen sections from three patients with renal allografts (two biopsies, one explant) with PVAN were analysed by indirect immunofluorescence using BKV specific anti-polyoma large T-antigen and anti-VP-1 antibodies, as well as anti-p53, anti-Ki67, anti-caspase-3, anti-bcl2 and anti-cytokeratin 22 antibodies. Nuclear morphology and size were estimated by DNA Hoechst staining. RESULTS: In infected tubular cells the early and late phases of infection could be distinguished according to expression of large T-antigen or VP-1. The early phase revealed almost normal nuclear proportions, whereas in later phases nuclear size increased about 2 to 3 fold. Expression of large T-antigen was strongly associated with accumulation of p53 in the nucleus, accompanied by the activation of the cell cycle associated cell protein Ki67. In contrast, expression of BKV VP1 correlated only weakly with p53. Virus dependent cell lysis was due to necrosis, since neither caspase 3 nor nuclear nor cytoskeleton changes indicated apoptosis. CONCLUSION: In our selected patients with PVAN a clear distinction between early and late phases was possible, according to the protein expression patterns of BKV markers. Striking nuclear enlargement is only present in the late phase of infection. In the inflammatory setting of PVAN, BKV dependent effects appear to be mediated by the inhibition of p53, resulting in the activation of the cell cycle. We assume that in PVAN similar BKV mechanisms are operative as in certain in vitro systems. |
| Databáze: | OpenAIRE |
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