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Published on: May 21, 2018
Emerging roles of rhomboid-like pseudoproteases in inflammatory and innate immune responses
1Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
Abstract:
Rhomboid-like pseudoproteases are a conserved superfamily of proteins related to the rhomboid intramembrane serine proteases that lack key catalytic residues. iRhom2, a member of the rhomboid-like pseudoprotease superfamily, regulates the maturation and trafficking of ADAM17 and is associated with inflammatory arthritis. Recent studies demonstrate that iRhom2 is also involved in innate immunity by regulating the trafficking and stability of MITA (also called STING), which is a central adaptor in innate antiviral signalling pathways. Here, we summarize recent progress on the roles and mechanisms of iRhom2 and its homologues in innate immunity and also discuss the links between the physiological functions of iRhoms and immunological diseases.
Insights
iRhom2, a pseudoprotease, regulates innate immunity by controlling MITA (STING) protein stability and trafficking. This protein is linked to inflammatory diseases and innate antiviral responses.
Area of Science:
- Molecular Biology
- Immunology
- Cell Biology
Background:
- Rhomboid-like pseudoproteases are related to serine proteases but lack catalytic activity.
- iRhom2, a pseudoprotease, influences ADAM17 processing and is implicated in inflammatory arthritis.
- Emerging evidence links iRhom2 to innate immunity pathways.
Purpose of the Study:
- To summarize recent findings on the roles and mechanisms of iRhom2 and its homologs in innate immunity.
- To discuss the connection between iRhom functions and immunological diseases.
Main Methods:
- Literature review of recent studies on iRhom2.
- Analysis of iRhom2's role in protein trafficking and stability.
- Exploration of iRhom2's involvement in innate immune signaling pathways.
Main Results:
- iRhom2 regulates the trafficking and stability of MITA (STING), a key innate antiviral signaling adaptor.
- iRhom2's functions extend beyond ADAM17 regulation into innate immune responses.
- Dysregulation of iRhom proteins is associated with immunological diseases.
Conclusions:
- iRhom2 plays a critical role in innate immunity by modulating MITA/STING.
- Understanding iRhom functions provides insights into the pathogenesis of immunological diseases.
- Further research into iRhoms could reveal new therapeutic targets for immune disorders.
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