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Updated: Jan 2, 2026

Characterization of MLKL-mediated Plasma Membrane Rupture in Necroptosis
Published on: August 7, 2018
Necroptosis in the Pathophysiology of Disease
Mitri K Khoury1, Kartik Gupta1, Sarah R Franco1
1Division of Vascular Surgery, Department of Surgery, University of Wisconsin-Madison, Madison, Wisconsin.
Abstract:
Over the past 15 years, elegant studies have demonstrated that in certain conditions, programed cell death resembles necrosis and depends on a unique molecular pathway with no overlap with apoptosis. This form of regulated necrosis is represented by necroptosis, in which the receptor-interacting protein kinase-3 and its substrate mixed-lineage kinase domain-like protein play a crucial role. With the development of knockout mouse models and molecular inhibitors unique to necroptotic proteins, this cell death has been found to occur in virtually all tissues and diseases evaluated. There are different immunologic consequences depending on whether cells die through apoptosis or necroptosis. Therefore, distinguishing between these two forms of cell death may be crucial during pathologic evaluations. In this review, we provide an understanding of necroptotic cell-death and highlight diseases in which necroptosis has been found to play a role. We also discuss the inhibitors of necroptosis and the ways these inhibitors have been used in preclinical models of diseases. These two discussions offer an understanding of the role of necroptosis in diseases and will foster efforts to pharmacologically target this unique yet pervasive form of programed cell death in the clinic.
Insights
Necroptosis, a programmed cell death resembling necrosis, involves specific proteins like RIPK3 and MLKL. Understanding this pathway is crucial for distinguishing it from apoptosis and targeting diseases.
Area of Science:
- Cell Biology
- Immunology
- Pathology
Background:
- Programmed cell death can occur via apoptosis or regulated necrosis.
- Necroptosis is a distinct form of programmed cell death with unique molecular pathways.
- Receptor-interacting protein kinase-3 (RIPK3) and mixed-lineage kinase domain-like protein (MLKL) are key mediators of necroptosis.
Purpose of the Study:
- To review the molecular mechanisms of necroptosis.
- To highlight the role of necroptosis in various diseases.
- To discuss necroptosis inhibitors and their preclinical applications.
Main Methods:
- Review of existing literature on necroptosis.
- Analysis of knockout mouse models and molecular inhibitors.
- Examination of necroptosis's role in different disease contexts.
Main Results:
- Necroptosis is a distinct cell death pathway with critical roles in numerous tissues and diseases.
- The immunologic consequences of necroptosis differ significantly from apoptosis.
- Necroptosis inhibitors have shown promise in preclinical disease models.
Conclusions:
- Distinguishing necroptosis from apoptosis is vital for accurate pathologic evaluation.
- Necroptosis is a pervasive cell death mechanism implicated in a wide range of diseases.
- Pharmacological targeting of necroptosis holds potential for future clinical applications.
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