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Complement Membrane Attack Complexes Disrupt Proteostasis to Function as Intracellular Alarmins
Dan Jane-Wit1, Guiyu Song2, Liying He1
1Yale University.
Research Square
|July 1, 2024
Summary
Membrane attack complexes (MACs) internalize, forming aggregates that trigger inflammation. This process involves C9 protein, aggrephagy, and ZFYVE21, revealing MACs as intracellular alarmins.
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- Membrane attack complexes (MACs) are known to cause cell lysis.
- Internalized MACs are implicated in NF-kB activation and tissue inflammation.
Purpose of the Study:
- To investigate the role of C9, a MAC-associated protein, in proteostasis and immune signaling.
- To elucidate the mechanism by which C9 aggregates induce inflammatory responses.
Main Methods:
- Utilized cell culture models and mouse models.
- Investigated protein aggregation, endocytosis, and aggrephagy pathways.
- Employed gene-deficient mice to study the role of ZFYVE21.
Main Results:
- Surface-bound C9 is internalized, aggregated within endosomes, and promotes loss of proteostasis.
- C9 aggregates stimulate NF-kB, inflammatory genes, and endothelial cell activation via aggrephagy.
- ZFYVE21 is crucial for C9 aggrephagy and stabilization of RNF34, impacting tissue injury.
Conclusions:
- C9 aggregates act as intracellular alarmins, linking MACs to inflammation beyond cytotoxicity.
- The C9-mediated aggrephagy pathway involving ZFYVE21 is a novel mechanism of immune activation.
- Targeting this pathway may offer therapeutic strategies for inflammatory diseases.
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