| Literature DB >> 30349078 |
Eui Ho Kim1, Sing-Wai Wong1,2, Jennifer Martinez3.
Abstract
Compared to the tidy and immunologically silent death during apoptosis, necrosis seems like a chaotic and unorganized demise. However, we now recognize that there is a method to its madness, as many forms of necrotic cell death are indeed programmed and function beyond lytic cell death to support homeostasis and immunity. Inherently more immunogenic than their apoptotic counterpart, programmed necrosis, such as necroptosis, pyroptosis, ferroptosis, and NETosis, releases inflammatory cytokines and danger-associated molecular patterns (DAMPs), skewing the milieu to a pro-inflammatory state. Moreover, impaired clearance of dead cells often leads to inflammation. Importantly, these pathways have all been implicated in inflammatory and autoimmune diseases, therefore careful understanding of their molecular mechanisms can have long lasting effects on how we interpret their role in disease and how we translate these mechanisms into therapy.Entities:
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Year: 2018 PMID: 30349078 PMCID: PMC6294794 DOI: 10.1038/s41418-018-0179-3
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 15.828