Self-regulation of the inflammatory response by peroxisome proliferator-activated receptors.

ABSTRACT: The peroxisome proliferator-activated receptor (PPAR) family includes three transcription factors: PPAR?, PPAR?/?, and PPAR?. PPAR are nuclear receptors activated by oxidised and nitrated fatty acid derivatives as well as by cyclopentenone prostaglandins (PGA2 and 15d-PGJ2) during the inflammatory response. This results in the modulation of the pro-inflammatory response, preventing it from being excessively activated. Other activators of these receptors are nonsteroidal anti-inflammatory drug (NSAID) and fatty acids, especially polyunsaturated fatty acid (PUFA) (arachidonic acid, ALA, EPA, and DHA). The main function of PPAR during the inflammatory reaction is to promote the inactivation of NF-?B. Possible mechanisms of inactivation include direct binding and thus inactivation of p65 NF-?B or ubiquitination leading to proteolytic degradation of p65 NF-?B. PPAR also exert indirect effects on NF-?B. They promote the expression of antioxidant enzymes, such as catalase, superoxide dismutase, or heme oxygenase-1, resulting in a reduction in the concentration of reactive oxygen species (ROS), i.e., secondary transmitters in inflammatory reactions. PPAR also cause an increase in the expression of I?B?, SIRT1, and PTEN, which interferes with the activation and function of NF-?B in inflammatory reactions.

SUBMITTER: Korbecki J 

PROVIDER: S-EPMC6517359 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature