4.6 Article

Antiviral Properties of Chemical Inhibitors of Cellular Anti-Apoptotic Bcl-2 Proteins

期刊

VIRUSES-BASEL
卷 9, 期 10, 页码 -

出版社

MDPI
DOI: 10.3390/v9100271

关键词

apoptosis; antiviral agent; innate immunity; host response

类别

资金

  1. JAMP
  2. A Erkko foundation
  3. European Regional Development Fund
  4. Mobilitas Pluss Project [MOBTT39]
  5. University of Helsinki [465/51/2014]
  6. Academy of Finland [SA259725]
  7. Sigrid Juselius Foundation
  8. Robert A. Welch Foundation [I-1422]
  9. University of Lille 2 [EA3610]
  10. CHRU Lille
  11. BioAMP
  12. Medical Technology Development Program of the NRF
  13. Ministry of Science, ICT and Future Planning, Republic of Korea [1601-0302]
  14. JAMP
  15. A Erkko foundation
  16. European Regional Development Fund
  17. Mobilitas Pluss Project [MOBTT39]
  18. University of Helsinki [465/51/2014]
  19. Academy of Finland [SA259725]
  20. Sigrid Juselius Foundation
  21. Robert A. Welch Foundation [I-1422]
  22. University of Lille 2 [EA3610]
  23. CHRU Lille
  24. BioAMP
  25. Medical Technology Development Program of the NRF
  26. Ministry of Science, ICT and Future Planning, Republic of Korea [1601-0302]

向作者/读者索取更多资源

Viral diseases remain serious threats to public health because of the shortage of effective means of control. To combat the surge of viral diseases, new treatments are urgently needed. Here we show that small-molecules, which inhibit cellular anti-apoptotic Bcl-2 proteins (Bcl-2i), induced the premature death of cells infected with different RNA or DNA viruses, whereas, at the same concentrations, no toxicity was observed in mock-infected cells. Moreover, these compounds limited viral replication and spread. Surprisingly, Bcl-2i also induced the premature apoptosis of cells transfected with viral RNA or plasmid DNA but not of mock-transfected cells. These results suggest that Bcl-2i sensitizes cells containing foreign RNA or DNA to apoptosis. A comparison of the toxicity, antiviral activity, and side effects of six Bcl-2i allowed us to select A-1155463 as an antiviral lead candidate. Thus, our results pave the way for the further development of Bcl-2i for the prevention and treatment of viral diseases.

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