Inhibitor of Apoptosis Protein cIAP2 Is Essential for Lipopolysaccharide-Induced Macrophage Survival

Author:

Conte Damiano12,Holcik Martin1,Lefebvre Charles A.3,LaCasse Eric3,Picketts David J.4,Wright Kathryn E.2,Korneluk Robert G.12

Affiliation:

1. Apoptosis Research Center, Children's Hospital of Eastern Ontario, Ottawa, K1H 8L1 Ontario, Canada

2. Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, K1H 8M5 Ontario, Canada

3. Ægera Oncology Inc., Ottawa, K1H 8L1 Ontario, Canada

4. Ottawa Health Research Institute, Ottawa, K1H 8L6 Ontario, Canada

Abstract

ABSTRACT The cellular inhibitor of apoptosis 2 (cIAP2/HIAP1) is a potent inhibitor of apoptotic death. In contrast to the other members of the IAP family, cIAP2 is transcriptionally inducible by nuclear factor-κB in response to multiple triggers. We demonstrate here that cIAP2 −/− mice exhibit profound resistance to lipopolysaccharide (LPS)-induced sepsis, specifically because of an attenuated inflammatory response. We show that LPS potently upregulates cIAP2 in macrophages and that cIAP2 −/− macrophages are highly susceptible to apoptosis in a LPS-induced proinflammatory environment. Hence, cIAP2 is critical in the maintenance of a normal innate immune inflammatory response.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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