Titlebook: Effector-Triggered Immunity; Methods and Protocol Thomas A. Kufer,Maria Kaparakis-Liaskos Book 2022 The Editor(s) (if applicable) and The A

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https://doi.org/10.57088/978-3-7329-9047-4omain-like receptors (NLRs) comprise 22 members, divided into 3 subfamilies. Homotypic pyrin domain (PYD) interactions were shown to mediate the interaction of inflammasome forming NLRPs with the adaptor protein ASC, bridging the interaction to caspase-1 and resulting in caspase-1-induced cytokine m

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https://doi.org/10.1007/978-3-658-19395-9 the assembly of inflammasomes, multimeric protein complexes that drive caspase-1 activation. Active caspase-1 cleaves the proinflammatory cytokines IL-1β and IL-18 and the pore-forming protein gasdermin-D (GSDMD) thereby liberating its N-terminal domain. The GSDMD N-termini form multimeric pores at

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https://doi.org/10.1007/978-3-642-51997-0ates the NLRP3 inflammasome to induce host pore-forming proteins and cellular suicide, termed pyroptosis. Host cell death rates are routinely determined at pre-defined time points and on whole cell populations. To capture the dynamic interactions between bacterial pore-forming toxins and host cell d

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Systematik der Elektronenger?tedamage. Although classically viewed as a discrete biochemical and cellular process in neutrophils, the effector pathways integrating diverse upstream activating signals to control the formation of NETs (NETosis) are poorly defined. Cell death is one such common unifying endpoint of neutrophils, with

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A Brief Introduction to Effector-Triggered Immunity,s is the key function of the innate immune systems of plants and mammals. Here we provide an introduction into pathogen recognition by the innate immune system of both plants and animals. We will particularly focus on the concept of effector-triggered immunity, and similarities and differences in its function between plants and animals.

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Effector-Triggered Immunity978-1-0716-2449-4Series ISSN 1064-3745 Series E-ISSN 1940-6029