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The role of PPARs in inflammation and immunity
Abstract
The family of transcription factors termed peroxisome proliferator-activated receptors (PPARs) has recently been the focus of much interest for their possible role in the regulation of inflammation and immune responses. PPARalpha and PPARgamma have been implicated in the regulation of macrophage and endothelial cell inflammatory responses. Although PPAR activation has generally been shown to have anti-inflammatory effects, opposite effects have been noted, and results often appear to depend on the ligands being used and the inflammatory parameters being measured. Recently, my laboratory and others have described a role for PPARgamma in the responses of T lymphocytes. Ligands for PPARgamma have been found to inhibit proliferation of activated T cells, and this appears to involve inhibition of IL-2 secretion and/or the induction of apoptosis. However, one problem in the interpretation of many of the studies of PPARgamma, inflammation, and immunity is that ligands thought to be specific for PPARgamma may have regulatory effects on inflammatory parameters that are PPARgamma-independent. Future studies of the role of the PPARs in inflammatory and immune responses should include further studies of T cells, T-cell subsets, and dendritic cells but will have to re-examine the issue of PPAR specificity of the ligands being used. This may require further knockout studies and technology, together with the identification of endogenous and perhaps more specific synthetic PPAR ligands.
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“Taken together, GW9662 influences genes in all classic PPARrelated metabolic pathways (lipid metabolism, glucose metabolism, immunity, and inflammation) (Clark, 2002;Wang, 2010).”
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Emerging roles of PPARS in inflammation and immunity
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Immunotoxicity of Perfluorinated Compounds: Recent Developments
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Metadata
- Authors
- Clark, R. B.
- Affiliations
- UConn Health (US)
- Corresponding author
- Clark, Robert B
- ORCID
- Clark, Robert B
- Venue
- Journal of Leukocyte Biology
- Publisher
- Oxford University Press (OUP)
- Published
- 2002-03-01
- Volume
- 71
- Issue
- 3
- Pages
- 388-400
- ISSN
- 0741-5400 (ISSN-L)
- 1938-3673
- OpenAlex
- W2167908723
- Cited by
- 337
- References
- 100
- Citations by year
- 2026: 1 · 2025: 6 · 2024: 5 · 2023: 7 · 2022: 7 · 2021: 5 · 2020: 14 · 2019: 15 · 2018: 10 · 2017: 15 · 2016: 15 · 2015: 21 · 2014: 23 · 2013: 11 · 2012: 10
- FWCI
- 7.76
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Leukocyte Biology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Health Sciences › Nursing › Nutrition and Dietetics › Fatty Acid Research and Health
- Keywords
- peroxisome proliferator-activated receptors, PPARγ, PPARα, inflammation, immune response, T cells, T cell proliferation, IL-2 secretion, apoptosis, macrophages, endothelial cells, PPAR ligands, ligand specificity, dendritic cells
- MeSH terms
- Animals, Humans, Immunity, Inflammation, Nuclear Proteins, Transcription Factors, Receptors, Cytoplasmic and Nuclear
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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