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A High Resolution Method to Monitor Phosphorylation-dependent Activation of IRF3
Published on: January 24, 2016
Grass carp (Ctenopharyngodon idellus) Cdc25a down-regulates IFN 1 expression by reducing TBK1 phosphorylation
Hang Deng1, Liugen Zeng2, Kaile Chang1
1College of Life Science, Nanchang University, Nanchang 330031, China.
Abstract:
In vertebrates, TANK Binding Kinase 1 (TBK1) plays an important role in innate immunity, mainly because it can mediate production of interferon to resist the invasion of pathogens. In mammals, cell division cycle-25a (Cdc25a) is a member of the Cdc25 family of cell division cycle proteins. It is a phosphatase that plays an important role in cell cycle regulation by dephosphorylating its substrate proteins. Currently, many phosphatases are reported to play a role in innate immunity. This is because the phosphatases can shut down or reduce immune signaling pathways by down-regulating phosphorylation signals. However, there are no reports on fish Cdc25a in innate immunity. In this paper, we conducted a preliminary study on the involvement of grass carp Cdc25a in innate immunity. First, we cloned the full-length cDNA of grass carp Cdc25a (CiCdc25a), and found that it shares the highest genetic relationship with that of Anabarilius grahami through phylogenetic tree comparison. In grass carp tissues and CIK cells, the expression of CiCdc25a mRNA was up-regulated under poly (I:C) stimulation. Therefore, CiCdc25a can respond to poly (I:C). The subcellular localization results showed that CiCdc25a is distributed both in the cytoplasm and nucleus. We also found that CiCdc25a can down-regulate the expression of IFN 1 with or without poly (I:C) stimulation. In other words, the down-regulation of IFN1 by CiCdc25a is independent of poly (I:C) stimulation. Further functional studies have shown that the inhibition of IFN1 expression by CiCdc25a may be related to decrease of TBK1 activity. We also confirmed that the phosphorylation of TBK1 at Ser172 is essential for production of IFN 1. In short, CiCdc25a can interact with TBK1 and subsequently inhibits the phosphorylation of TBK1, thereby weakens TBK1 activity. These results indicated that grass carp Cdc25a down-regulates IFN 1 expression by reducing TBK1 phosphorylation.
Insights
Grass carp Cdc25a (CiCdc25a) responds to immune stimulation and inhibits interferon production by reducing TANK Binding Kinase 1 (TBK1) activity. This study reveals a novel role for Cdc25a in fish innate immunity.
Area of Science:
- Immunology
- Molecular Biology
- Fish Biology
Background:
- TANK Binding Kinase 1 (TBK1) is crucial for innate immunity in vertebrates, mediating interferon production against pathogens.
- Cell division cycle-25a (Cdc25a) phosphatases regulate cell cycles and are increasingly recognized for roles in innate immunity by modulating signaling pathways.
- The role of fish Cdc25a in innate immunity remains unexplored.
Purpose of the Study:
- To investigate the involvement of grass carp Cdc25a (CiCdc25a) in innate immunity.
- To elucidate the mechanism by which CiCdc25a affects interferon 1 (IFN1) expression and TBK1 activity.
Main Methods:
- Cloning of grass carp Cdc25a full-length cDNA.
- Phylogenetic analysis to determine genetic relationships.
- mRNA expression analysis in grass carp tissues and CIK cells under poly (I:C) stimulation.
- Subcellular localization studies.
- Functional assays to assess CiCdc25a's effect on IFN1 expression and TBK1 activity.
Main Results:
- Grass carp Cdc25a (CiCdc25a) mRNA expression was upregulated by poly (I:C) stimulation.
- CiCdc25a down-regulates IFN1 expression independently of poly (I:C) stimulation.
- CiCdc25a interacts with TBK1, inhibiting its phosphorylation at Ser172 and consequently weakening TBK1 activity.
Conclusions:
- Grass carp Cdc25a plays a role in innate immunity by negatively regulating IFN1 expression.
- CiCdc25a exerts its inhibitory effect through the modulation of TBK1 phosphorylation and activity.
- This study establishes a novel mechanism of immune regulation involving Cdc25a and TBK1 in fish.
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