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Poly(ADP-Ribose) Polymerases in Host-Pathogen Interactions, Inflammation, and Immunity.
Pamlea N Brady1, Anupam Goel2, Margaret A Johnson3
1Department of Chemistry, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Microbiology and Molecular Biology Reviews : MMBR
|December 21, 2018
Summary
Poly(ADP-ribose) polymerase (PARP) enzymes are crucial in host-pathogen interactions and inflammation. PARP inhibitors offer potential therapeutic benefits for inflammatory diseases like diabetes and arthritis.
Area of Science:
- Biochemistry
- Immunology
- Molecular Biology
Background:
- The poly(ADP-ribose) polymerase (PARP) family comprises 17 enzymes with diverse biological roles.
- PARP1 is the most studied human PARP enzyme, involved in numerous cellular processes.
- PARP enzymes play significant roles in host-pathogen interactions and inflammatory responses.
Purpose of the Study:
- To review recent research on PARP enzyme functions.
- To focus on the involvement of PARPs in host-pathogen interactions and inflammatory diseases.
- To highlight the potential of PARP inhibitors as therapeutic agents.
Main Methods:
- Literature review of recent research on PARP family proteins.
- Analysis of PARP roles in mammalian antiviral responses (e.g., PARP13/ZAP).
- Examination of PARP involvement in plant immunity and stress responses.
Main Results:
- PARP enzymes are implicated in both host defense and pathogen evasion.
- PARPs modulate inflammatory signaling pathways, leading to cytokine and adhesion molecule expression.
- PARP13 (ZAP) is a key player in the mammalian antiviral response.
- Poly(ADP-ribosyl)ation regulates plant stress responses and immunity.
Conclusions:
- PARP enzymes are critical regulators of host-pathogen interactions and inflammatory processes.
- PARP inhibitors demonstrate therapeutic potential for inflammatory conditions such as diabetes, arthritis, and stroke.
- Understanding PARP functions provides insights into disease pathogenesis and host responses, aiding in inhibitor development.
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