Inhibition of interleukin 1β-converting enzyme-mediated apoptosis of mammalian cells by baculovirus IAP

Christine J. Hawkins*, Anthony G. Uren, Georg Häcker, Robert L. Medcalf, David L. Vaux

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

<jats:p>Apoptosis can be a potent weapon against viral infection and consequently has selected for viruses carrying antiapoptosis genes. Two baculovirus proteins, IAP and p35, can prevent insect cells from dying in response to infection. p35, which interferes with members of the Ced-3 family of cysteine proteases, can also function in mammalian cells. We investigated the ability of IAP from<jats:italic>Orgyia pseudotsugata</jats:italic>nuclear polyhedrosis virus to prevent death of mammalian cells. IAP was transiently expressed in mammalian cells and its ability to block cell death caused by expression of interleukin-1β converting enzyme (ICE), FADD, or the ICE homologues ICH-1 and ICE-Lap3, was investigated. IAP strongly inhibited ICE- and ICH-1-induced cell death but protected only partially against death by overexpression of FADD and not at all against death due to enforced ICE-Lap3 expression. These results demonstrate that a baculoviral IAP protein can functionally interact with conserved components of the apoptosis machinery in mammalian cells.</jats:p>
Original languageEnglish
Pages (from-to)13786-13790
Number of pages0
JournalProceedings of the National Academy of Sciences
Volume93
Issue number24
DOIs
Publication statusPublished - 26 Nov 1996

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