Human Cytomegalovirus Induces Drug Resistance and Alteration of Programmed Cell Death by Accumulation of ΔN-p73α
| Autor: | Daniel Caput, Sophie Allart, Claire Détraves, Jérôme Terrasson, Hélène Martin, Christian Davrinche |
|---|---|
| Rok vydání: | 2002 |
| Předmět: |
Human cytomegalovirus
Programmed cell death Microcephaly Transcription Genetic Cell Survival viruses Blotting Western Cytomegalovirus Lissencephaly Apoptosis Biology Biochemistry Cell Line Atrophy Cell Movement Drug Resistance Viral Tumor Cells Cultured medicine Humans Protein Isoforms Genes Tumor Suppressor neoplasms Molecular Biology Tropism Fetus Reverse Transcriptase Polymerase Chain Reaction Tumor Suppressor Proteins Nuclear Proteins Tumor Protein p73 Cell Biology medicine.disease Up-Regulation DNA-Binding Proteins Microscopy Fluorescence Immunology Cisplatin Tumor Suppressor Protein p53 Protein Binding |
| Zdroj: | Journal of Biological Chemistry. 277:29063-29068 |
| ISSN: | 0021-9258 |
| Popis: | Intrauterine transmission of human cytomegalovirus (HCMV) to the fetus following primary infection in early and late pregnancy usually results in severe neurological handicaps and sensorineural hearing loss with typical migrational anomalies, optic atrophy, disturbed myelination, cerebella hypoplasia, microcephaly, hydrocephaly, and lissencephaly. Recently, evidences raised from the phenotype of p73-deficient mice show that an association may exist between the expression of the TP53 homologous gene and HCMV tropism in the brain, suggesting an implication of p73 in viral persistence. In this study, we demonstrated that HCMV-mediated inhibition of apoptosis only occurs in p73-expressing cells. Upon infection, an accumulation of deltaN-p73alpha isoforms was observed in HCMV-infected p73-positive cells. This phenomenon was shown to be responsible for the subsequent acquired resistance to apoptosis of infected cells. Inhibition of apoptosis in p73-positive cells by HCMV may thus contribute both to virus persistency and abnormal nervous cell survival. This finding provides the first molecular basis for HCMV-associated abnormal embryonic development and neurological defects in newborns. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|