Caspase-8, the initiator caspase of the death receptor pathway of apoptosis, is critically required for murine embryonic development;animals lacking this caspase die around e10.5. This lethality cannot be attributed to a defect in apoptosis;leading to the idea that caspase-8 has an independent survival function. Recently we showed that development in caspase-8-deficient animals is fully rescued by ablation of RIPK3, a kinase that triggers a programmed form of necrosis (sometimes called "necroptosis"). In vitro studies showed that a complex of an adapter, FADD, caspase-8, and the caspase-8-like molecule FLIP, associates with RIPK3 (and another kinase, RIPK1), and the proteolytic activity of caspase-8-FLIP then prevents RIPK-dependent necrosis. Intriguingly, knockout of either FADD or FLIP causes the same embryonic lethality observed in caspase-8- deficient mice. Our central hypothesis, upon which this application is based, is that a complex of the adapter molecule, FADD, caspase-8, and FLIP, while not promoting apoptosis, antagonizes the formation of a necrosis-inducing RIPK1-RIPK3 complex, and thereby protects cells and animal development-this is the primary auxiliary (survival) role for FADD, FLIP, and caspase-8. Based on this hypothesis, we propose: 1. to formally test a model of FADD, FLIP, and caspase-8-mediated survival. Here, we will investigate the roles of FADD, FLIP, and caspase-8 in promoting and/or preventing apoptosis and RIPK-dependent lethality in development and in adult animals. Our model makes a number of predictions that will be tested in vivo and in vitro. 2. To investigate how the FADD-Caspase-8-FLIP complex antagonizes the RIPK1-RIPK3 complex function without inducing apoptosis. The catalytic activity of caspase-8 is required for cell survival. We will test three possibilities (which are not mutually exclusive): a. that caspase-8-FLIP has a different specificity than pro-apoptotic caspase-8 homodimers;b) that caspase-8-FLIP and caspase-8 homodimers have different access to substrates;and/or that caspase-8-FLIP heterodimers and caspase-8 homodimers differentially target caspase-8 and RIPK1-RIPK3 for degradation or inactivating modifications. We will perform our studies by utilizing potential substrates for caspase-8-FLIP and caspase-8 homodimers and determine if cleavage is required for protective effects. Our studies test these possibilities in vitro and in vivo.3. To delineate the mechanism(s) of RIPK-dependent necrosis. Using a novel system in which RIPK3 kinase activity induces necrosis independently of caspase or RIPK1 activity we will perform candidate and unbiased approaches to identify the mechanisms of this rapid, active necrosis. The finding that caspase-8-RIPK3 double knockout (DKO) mice are developmentally normal is a "game changer" that demands that the many proposed roles for FADD, caspase-8, and FLIP in cellular processes be rigorously re-examined with the possibility that all such effects are a direc outcome of the regulatory interactions between the FADD-caspase-8-FLIP complex and the RIPK1-RIPK3 function in triggering necrosis (and possibly other cellular effects of RIPK3). The experiments proposed in this application will provide such a re-evaluation, while providing deep insights into the mechanisms and regulation of RIPK-dependent necrosis.

Public Health Relevance

Cell death is crucial for normal homeostasis, and defects in this process underlie many human diseases. This project explores how cell death is controlled at the level of precise molecular interactions, amenable to pharmacologic manipulation, testing a new model of this process in development and the immune response.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI044828-15
Application #
8464621
Study Section
Cellular Signaling and Regulatory Systems Study Section (CSRS)
Program Officer
Leitner, Wolfgang W
Project Start
1999-03-01
Project End
2017-04-30
Budget Start
2013-05-01
Budget End
2014-04-30
Support Year
15
Fiscal Year
2013
Total Cost
$411,250
Indirect Cost
$176,250
Name
St. Jude Children's Research Hospital
Department
Type
DUNS #
067717892
City
Memphis
State
TN
Country
United States
Zip Code
38105
Green, Douglas R; Levine, Beth (2014) To be or not to be? How selective autophagy and cell death govern cell fate. Cell 157:65-75
Newton, Kim; Hildebrand, Joanne M; Shen, Zhirong et al. (2014) Is SIRT2 required for necroptosis? Nature 506:E4-6
Shenderov, Kevin; Riteau, Nicolas; Yip, Ronald et al. (2014) Cutting edge: Endoplasmic reticulum stress licenses macrophages to produce mature IL-1? in response to TLR4 stimulation through a caspase-8- and TRIF-dependent pathway. J Immunol 192:2029-33
Linkermann, Andreas; Green, Douglas R (2014) Necroptosis. N Engl J Med 370:455-65
Dillon, Christopher P; Weinlich, Ricardo; Rodriguez, Diego A et al. (2014) RIPK1 blocks early postnatal lethality mediated by caspase-8 and RIPK3. Cell 157:1189-202
Linkermann, Andreas; Skouta, Rachid; Himmerkus, Nina et al. (2014) Synchronized renal tubular cell death involves ferroptosis. Proc Natl Acad Sci U S A 111:16836-41
Weinlich, Ricardo; Green, Douglas R (2014) The two faces of receptor interacting protein kinase-1. Mol Cell 56:469-80
Gurung, Prajwal; Anand, Paras K; Malireddi, R K Subbarao et al. (2014) FADD and caspase-8 mediate priming and activation of the canonical and noncanonical Nlrp3 inflammasomes. J Immunol 192:1835-46
Green, Douglas R; Galluzzi, Lorenzo; Kroemer, Guido (2014) Cell biology. Metabolic control of cell death. Science 345:1250256
Weinlich, Ricardo; Oberst, Andrew; Dillon, Christopher P et al. (2013) Protective roles for caspase-8 and cFLIP in adult homeostasis. Cell Rep 5:340-8

Showing the most recent 10 out of 38 publications