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Updated: Jun 22, 2025

Characterization of MLKL-mediated Plasma Membrane Rupture in Necroptosis
Published on: August 7, 2018
ChRIPK1 caused necroptosis signaling pathway deficiency in Crassostrea hongkongensis
Yucheng Yang1, Liang Zeng1, Tianxiang Lin1
1Key Laboratory of Breeding Biotechnology and Sustainable Aquaculture, Key Laboratory of Tropical Marine Bioresources and Ecology, Guangdong Provincial Key Laboratory of Applied Marine Biology, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
Abstract:
RIPK1/TAK1 are important for programmed cell death, including liver death, necroptosis and apoptosis. However, there have been few published reports on the functions of RIPK1/TAK1 in invertebrates. In this study, full-length ChRIPK1 and ChTAK1 were cloned from C. hongkongensis through the rapid amplification of cDNA ends (RACE) technology. ChRIPK1 has almost no homology with human RIPK1 and lacks a kinase domain at the N-terminus but has a DD and RHIM domain. ChTAK1 is conserved throughout evolution. qRT‒PCR was used to analyze the mRNA expression patterns of ChRIPK1 in different tissues, developmental stages, and V. coralliilyticus-infected individuals, and both were highly expressed in the mantle and gills, while ChRIPK1 was upregulated in hemocytes and gills after V. coralliilyticus or S. aureus infection, which indicates that ChRIPK1 is involved in immune regulation. Fluorescence assays revealed that ChRIPK1 localized to the cytoplasm of HEK293T cells in a punctiform manner, but the colocalization of ChRIPK1 with ChTAK1 abolished the punctiform morphology. In the dual-luciferase reporter assay, both ChRIPK1 and ChRIPK1-RIHM activated the NF-κB signaling pathway in HEK293T cells, and ChTAK1 activated ChRIPK1 in the NF-κB signaling pathway. The apoptosis rate of the hemocytes was not affected by the necroptosis inhibitor Nec-1 but was significantly decreased, and ChRIPK1 expression was knocked down in the hemocytes of C. hongkongensis. These findings indicated that ChRIPK1 induces apoptosis but not necroptosis in oysters. This study provides a theoretical basis for further research on the molecular mechanism by which invertebrates regulate the programmed cell death of hemocytes in oysters.
Insights
This study cloned oyster genes ChRIPK1 and ChTAK1, revealing ChRIPK1 regulates programmed cell death in oyster hemocytes, specifically inducing apoptosis, not necroptosis, and plays a role in immune responses.
Area of Science:
- * Molecular Biology
- * Immunology
- * Invertebrate Zoology
Background:
- * Receptor-interacting protein kinase 1 (RIPK1) and Transforming growth factor beta-activated kinase 1 (TAK1) are crucial in programmed cell death pathways like necroptosis and apoptosis.
- * Limited research exists on RIPK1/TAK1 functions in invertebrates, particularly in bivalves.
Purpose of the Study:
- * To clone and characterize oyster (C. hongkongensis) RIPK1 (ChRIPK1) and TAK1 (ChTAK1).
- * To investigate the roles of ChRIPK1 and ChTAK1 in programmed cell death and immune regulation in oysters.
Main Methods:
- * Rapid amplification of cDNA ends (RACE) for gene cloning.
- * Quantitative reverse transcription PCR (qRT-PCR) for gene expression analysis.
- * Fluorescence assays, dual-luciferase reporter assays, and knockdown experiments.
Main Results:
- * ChRIPK1 shares limited homology with human RIPK1, lacking an N-terminal kinase domain but possessing DD and RHIM domains.
- * ChRIPK1 and ChTAK1 are highly expressed in oyster mantle and gills; ChRIPK1 is upregulated in hemocytes and gills upon bacterial infection.
- * ChRIPK1 activates the NF-κB signaling pathway and induces apoptosis, but not necroptosis, in oyster hemocytes.
Conclusions:
- * ChRIPK1 is involved in immune regulation and programmed cell death in oysters.
- * ChRIPK1 induces apoptosis in oyster hemocytes, independent of necroptosis pathways.
- * Findings provide a foundation for understanding invertebrate programmed cell death mechanisms.
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