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1000 Titel
  • 3D culture conditions support Kaposi’s sarcoma herpesvirus (KSHV) maintenance and viral spread in endothelial cells
1000 Autor/in
  1. Dubich, Tatyana |
  2. Dittrich, Anne |
  3. Bousset, Kristine |
  4. Geffers, Robert |
  5. Büsche, Guntram |
  6. Köster, Mario |
  7. Hauser, Hansjörg |
  8. Schulz, Thomas F. |
  9. Wirth, Dagmar |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-01-23
1000 Erschienen in
1000 Quellenangabe
  • 99(3):425-438
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00109-020-02020-8 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900040/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Kaposi's sarcoma-associated herpesvirus (KSHV) is a human tumorigenic virus and the etiological agent of an endothelial tumor (Kaposi's sarcoma) and two B cell proliferative diseases (primary effusion lymphoma and multicentric Castleman's disease). While in patients with late stage of Kaposi's sarcoma the majority of spindle cells are KSHV-infected, viral copies are rapidly lost in vitro, both upon culture of tumor-derived cells or from newly infected endothelial cells. We addressed this discrepancy by investigating a KSHV-infected endothelial cell line in various culture conditions and in tumors of xenografted mice. We show that, in contrast to two-dimensional endothelial cell cultures, KSHV genomes are maintained under 3D cell culture conditions and in vivo. Additionally, an increased rate of newly infected cells was detected in 3D cell culture. Furthermore, we show that the PI3K/Akt/mTOR and ATM/γH2AX pathways are modulated and support an improved KSHV persistence in 3D cell culture. These mechanisms may contribute to the persistence of KSHV in tumor tissue in vivo and provide a novel target for KS specific therapeutic interventions. KEY MESSAGES: In vivo maintenance of episomal KSHV can be mimicked in 3D spheroid cultures 3D maintenance of KSHV is associated with an increased de novo infection frequency PI3K/Akt/mTOR and ATM/ γH2AX pathways contribute to viral maintenance.
1000 Sacherschließung
lokal Cell Culture Techniques, Three Dimensional [MeSH]
lokal KSHV infected endothelial cells
lokal Cell Line [MeSH]
lokal Virus Release [MeSH]
lokal Phosphatidylinositol 3-Kinases/physiology [MeSH]
lokal Spheroids, Cellular/transplantation [MeSH]
lokal Virus Replication [MeSH]
lokal Episomal viral genomes
lokal Original Article
lokal Endothelial Cells/virology [MeSH]
lokal Signal Transduction/physiology [MeSH]
lokal Xenograft model
lokal Ataxia Telangiectasia Mutated Proteins/physiology [MeSH]
lokal Herpesvirus 8, Human/physiology [MeSH]
lokal Virus Cultivation/methods [MeSH]
lokal Viral maintenance
lokal Cell Division/drug effects [MeSH]
lokal 3D culture
lokal Endothelial Cells/cytology [MeSH]
lokal Humans [MeSH]
lokal TOR Serine-Threonine Kinases/physiology [MeSH]
lokal Cell Line, Transformed [MeSH]
lokal Doxycycline/pharmacology [MeSH]
lokal Heterografts [MeSH]
lokal Animals [MeSH]
lokal Mice [MeSH]
lokal Virus Latency [MeSH]
lokal Genome, Viral [MeSH]
lokal Spheroids, Cellular/virology [MeSH]
lokal Proto-Oncogene Proteins c-akt/physiology [MeSH]
lokal Plasmids [MeSH]
lokal Histones/physiology [MeSH]
lokal Sarcoma, Kaposi/virology [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/RHViaWNoLCBUYXR5YW5h|https://frl.publisso.de/adhoc/uri/RGl0dHJpY2gsIEFubmU=|https://frl.publisso.de/adhoc/uri/Qm91c3NldCwgS3Jpc3RpbmU=|https://frl.publisso.de/adhoc/uri/R2VmZmVycywgUm9iZXJ0|https://frl.publisso.de/adhoc/uri/QsO8c2NoZSwgR3VudHJhbQ==|https://frl.publisso.de/adhoc/uri/S8O2c3RlciwgTWFyaW8=|https://frl.publisso.de/adhoc/uri/SGF1c2VyLCBIYW5zasO2cmc=|https://frl.publisso.de/adhoc/uri/U2NodWx6LCBUaG9tYXMgRi4=|https://orcid.org/0000-0002-2541-6251
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1000 Erstellt am 2023-05-03T18:04:01.248+0200
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1000 Zuletzt bearbeitet Fri Oct 20 22:24:42 CEST 2023
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