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Amino-acid sensing and degrading pathways in immune regulation.
- Source :
-
Cytokine & growth factor reviews [Cytokine Growth Factor Rev] 2017 Jun; Vol. 35, pp. 37-45. Date of Electronic Publication: 2017 May 18. - Publication Year :
- 2017
-
Abstract
- Indoleamine 2,3-dioxygenases (IDOs) - belonging in the heme dioxygenase family and degrading tryptophan - are responsible for the de novo synthesis of nicotinamide adenine dinucleotide (NAD <superscript>+</superscript> ). As such, they are expressed by a variety of invertebrate and vertebrate species. In mammals, IDO1 has remarkably evolved to expand its functions, so to become a prominent homeostatic regulator, capable of modulating infection and immunity in multiple ways, including local tryptophan deprivation, production of biologically active tryptophan catabolites, and non-enzymatic cell-signaling activity. Much like IDO1, arginase 1 (Arg1) is an immunoregulatory enzyme that catalyzes the degradation of arginine. Here, we discuss the possible role of amino-acid degradation as related to the evolution of the immune systems and how the functions of those enzymes are linked by an entwined pathway selected by phylogenesis to meet the newly arising needs imposed by an evolving environment.<br /> (Copyright © 2017 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Subjects :
- Animals
Arginase metabolism
Dendritic Cells enzymology
Gene Expression Regulation
Humans
Indoleamine-Pyrrole 2,3,-Dioxygenase genetics
Indoleamine-Pyrrole 2,3,-Dioxygenase metabolism
Interferon-gamma immunology
Interleukin-4 immunology
Mice
Neoplasms immunology
Neoplasms metabolism
Signal Transduction
Transforming Growth Factor beta1 immunology
Tryptophan metabolism
Amino Acids metabolism
Dendritic Cells immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0305
- Volume :
- 35
- Database :
- MEDLINE
- Journal :
- Cytokine & growth factor reviews
- Publication Type :
- Academic Journal
- Accession number :
- 28545736
- Full Text :
- https://doi.org/10.1016/j.cytogfr.2017.05.004