Amino-acid sensing and degrading pathways in immune regulation

被引:72
作者
Grohmann, Ursula [1 ]
Mondanelli, Giada [1 ]
Belladonna, Maria L. [1 ]
Orabona, Ciriana [1 ]
Pallotta, Maria T. [1 ]
Iacono, Alberta [1 ]
Puccetti, Paolo [1 ]
Volpi, Claudia [1 ]
机构
[1] Univ Perugia, Dept Expt Med, I-06132 Perugia, Italy
基金
欧洲研究理事会;
关键词
Arg1; IDO1; Immune regulation; Dendritic cell; ARYL-HYDROCARBON RECEPTOR; DENDRITIC CELLS; INDOLEAMINE 2,3-DIOXYGENASE; TRYPTOPHAN CATABOLISM; T-CELLS; ARGININE METABOLISM; NITRIC-OXIDE; CANCER; TOLERANCE; DISEASE;
D O I
10.1016/j.cytogfr.2017.05.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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(+)). 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. (c) 2017 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:37 / 45
页数:9
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