Biochemical and medical aspects of the indoleamine 2,3-dioxygenase-initiated L-tryptophan metabolism

被引:275
作者
Takikawa, O [1 ]
机构
[1] Natl Ctr Geriatr & Gerontol, Natl Inst Longev Sci, Aichi 4748522, Japan
关键词
heme-containing dioxygenase; tryptophan; interferon-7; immunosuppression; dendritic cells; quinolinic acid; Alzheimer's disease; age-related cataract; kynurenilation; neurotoxin; metabolism; indoleamine dioxygenase;
D O I
10.1016/j.bbrc.2005.09.032
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-dioxygenase (EC 1.13.11.42) is a heme-containing dioxygenase which catalyzes the first and rate-limiting step in the major pathway of L-tryptophan catabolism in mammals. Much attention has recently been focused on the dioxygenase because this metabolic pathway is involved not only in a variety of physiological functions but also in many diseases. In this review, the discovery and unique catalytic properties of dioxygenase are described first, and then the recent findings regarding the dioxygenase-initiated tryptophan metabolism are summarized, with special emphasis on the detrimental role of dioxygenase in side effects of interferon-gamma and interleukin-12 (by systemic tryptophan depletion), the escape of malignant tumors from immune surveillance (by immunosuppression caused by tryptophan depletion), several neurodegenerative disorders including Alzheimer's disease (by an aberrant production of neurotoxin, quinolinic acid), and age-related cataract (due to "Kynurenilation," a novel post-translational modification of lens proteins with tryptophan-derived UV filters). (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:12 / 19
页数:8
相关论文
共 87 条
[11]   INDUCTION OF TRYPTOPHAN CATABOLISM IS THE MECHANISM FOR GAMMA-INTERFERON-MEDIATED INHIBITION OF INTRACELLULAR CHLAMYDIA-PSITTACI REPLICATION IN T24 CELLS [J].
BYRNE, GI ;
LEHMANN, LK ;
LANDRY, GJ .
INFECTION AND IMMUNITY, 1986, 53 (02) :347-351
[12]   MOLECULAR-CLONING, SEQUENCING AND EXPRESSION OF HUMAN INTERFERON-GAMMA-INDUCIBLE INDOLEAMINE 2,3-DIOXYGENASE CDNA [J].
DAI, W ;
GUPTA, SL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 168 (01) :1-8
[13]   THE ROLE OF HYDROGEN-PEROXIDE IN THE INVITRO CYTOTOXICITY OF 3-HYDROXYKYNURENINE [J].
EASTMAN, CL ;
GUILARTE, TR .
NEUROCHEMICAL RESEARCH, 1990, 15 (11) :1101-1107
[14]   Engineered vascular-targeting antibody-interferon-γ fusion protein for cancer therapy [J].
Ebbinghaus, C ;
Ronca, R ;
Kaspar, M ;
Grabulovski, D ;
Berndt, A ;
Kosmehl, H ;
Zardi, L ;
Neri, D .
INTERNATIONAL JOURNAL OF CANCER, 2005, 116 (02) :304-313
[15]   PREVALENCE OF ALZHEIMERS-DISEASE IN A COMMUNITY POPULATION OF OLDER PERSONS - HIGHER THAN PREVIOUSLY REPORTED [J].
EVANS, DA ;
FUNKENSTEIN, H ;
ALBERT, MS ;
SCHERR, PA ;
COOK, NR ;
CHOWN, MJ ;
HEBERT, LE ;
HENNEKENS, CH ;
TAYLOR, JO .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1989, 262 (18) :2551-2556
[16]   SELECTIVE OXIDATION OF CYSTEINE AND METHIONINE IN NORMAL AND SENILE CATARACTOUS LENSES [J].
GARNER, MH ;
SPECTOR, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (03) :1274-1277
[17]   Indoleamine 2,3 dioxygenase and quinolinic acid immunoreactivity in Alzheimer's disease hippocampus [J].
Guillemin, GJ ;
Brew, BJ ;
Noonan, CE ;
Takikawa, O ;
Cullen, KM .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2005, 31 (04) :395-404
[18]   AβI-42 induces production of quinolinic acid by human macrophages and microglia [J].
Guillemin, GJ ;
Smythe, GA ;
Veas, LA ;
Takikawa, O ;
Brew, BJ .
NEUROREPORT, 2003, 14 (18) :2311-2315
[19]  
HABARAOHKUBO A, 1991, GENE, V105, P221, DOI 10.1016/0378-1119(91)90154-4
[20]   MECHANISM OF THE PYROCATECHASE REACTION [J].
HAYAISHI, O ;
KATAGIRI, M ;
ROTHBERG, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (20) :5450-5451