Selenium and selenoproteins in prostanoid metabolism and immunity.


Journal

Critical reviews in biochemistry and molecular biology
ISSN: 1549-7798
Titre abrégé: Crit Rev Biochem Mol Biol
Pays: England
ID NLM: 8903774

Informations de publication

Date de publication:
12 2019
Historique:
pubmed: 31 1 2020
medline: 26 3 2020
entrez: 31 1 2020
Statut: ppublish

Résumé

Selenium (Se) is an essential trace element that functions in the form of the 21st amino acid, selenocysteine (Sec) in a defined set of proteins. Se deficiency is associated with pathological conditions in humans and animals, where incorporation of Sec into selenoproteins is reduced along with their expression and catalytic activity. Supplementation of Se-deficient population with Se has shown health benefits suggesting the importance of Se in physiology. An interesting paradigm to explain, in part, the health benefits of Se stems from the observations that selenoprotein-dependent modulation of inflammation and efficient resolution of inflammation relies on mechanisms involving a group of bioactive lipid mediators, prostanoids, which orchestrate a concerted action toward maintenance and restoration of homeostatic immune responses. Such an effect involves the interaction of various immune cells with these lipid mediators where cellular redox gatekeeper functions of selenoproteins further aid in not only dampening inflammation, but also initiating an effective and active resolution process. Here we have summarized the current literature on the multifaceted roles of Se/selenoproteins in the regulation of these bioactive lipid mediators and their immunomodulatory effects.

Identifiants

pubmed: 31996052
doi: 10.1080/10409238.2020.1717430
pmc: PMC7122104
mid: NIHMS1566915
doi:

Substances chimiques

Prostaglandins 0
Selenoproteins 0
Selenium H6241UJ22B

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

484-516

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK077152
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK119865
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA162665
Pays : United States

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Auteurs

Fenghua Qian (F)

Center for Molecular Immunology and Infectious Disease, The Pennsylvania State University, PA, USA.
Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University, PA, USA.
Department of Veterinary and Biomedical Sciences, The Pennsylvania State University, PA, USA.
The Penn State Cancer Institute, The Pennsylvania State University, PA, USA.

Sougat Misra (S)

Center for Molecular Immunology and Infectious Disease, The Pennsylvania State University, PA, USA.
Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University, PA, USA.
Department of Veterinary and Biomedical Sciences, The Pennsylvania State University, PA, USA.
The Penn State Cancer Institute, The Pennsylvania State University, PA, USA.

K Sandeep Prabhu (KS)

Center for Molecular Immunology and Infectious Disease, The Pennsylvania State University, PA, USA.
Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University, PA, USA.
Department of Veterinary and Biomedical Sciences, The Pennsylvania State University, PA, USA.
The Penn State Cancer Institute, The Pennsylvania State University, PA, USA.

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