The circadian clock circuitry and the AHR signaling pathway in physiology and pathology

被引:43
作者
Anderson, George [1 ]
Beischlag, Timothy V. [2 ]
Vinciguerra, Manlio [3 ]
Mazzoccoli, Gianluigi [4 ,5 ,6 ]
机构
[1] Clin Res Ctr Commun, Glasgow, Lanark, Scotland
[2] Simon Fraser Univ, Fac Hlth Sci, Burnaby, BC V5A 1S6, Canada
[3] UCL, Inst Liver & Digest Hlth, Div Med, London, England
[4] IRCCS Sci Inst, Div Internal Med, Dept Med Sci, San Giovanni Rotondo, FG, Italy
[5] IRCCS Sci Inst, Chronobiol Unit, San Giovanni Rotondo, FG, Italy
[6] Reg Gen Hosp Casa Sollievo Sofferenza, San Giovanni Rotondo, FG, Italy
关键词
AHR; ARNT; Clock gene; Circadian rhythm; ARYL-HYDROCARBON RECEPTOR; INFLAMMATORY-BOWEL-DISEASE; BREAST-CANCER RISK; KAPPA-B INTERACTIONS; NIGHT-SHIFT WORK; PROSTATE-CANCER; GENE-EXPRESSION; INTESTINAL INFLAMMATION; INTRACELLULAR CALCIUM; TRANSCRIPTION FACTORS;
D O I
10.1016/j.bcp.2013.02.022
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Life forms populating the Earth must face environmental challenges to assure individual and species survival. The strategies predisposed to maintain organismal homeostasis and grant selective advantage rely on anticipatory phenomena facing periodic modifications, and compensatory phenomena facing unpredictable changes. Biological processes bringing about these responses are respectively driven by the circadian timing system, a complex of biological oscillators entrained to the environmental light/dark cycle, and by regulatory and metabolic networks that precisely direct the body's adjustments to variations of external conditions and internal milieu. A critical role in organismal homeostatic functions is played by the aryl hydrocarbon receptor (AHR) complex, which senses environmental and endogenous compounds, influences metabolic responses controlling phase I/II gene expression, and modulates vital phenomena such as development, inflammation and adaptive immunity. A physiological cross-talk between circadian and AHR signaling pathways has been evidenced. The alteration of AHR signaling pathway deriving from genetic damage with polymorphisms or mutations, or produced by exogenous or endogenous AHR activation, and chronodisruption caused by mismatch between the body's internal clock and geophysical time/social schedules, are capable of triggering pathological mechanisms involved in metabolic, immune-related and neoplastic diseases. On the other hand, the molecular components of the circadian clock circuitry and AHR signaling pathway may represent useful tools for preventive interventions and valuable targets of therapeutic approaches. (c) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:1405 / 1416
页数:12
相关论文
共 151 条
[1]  
Agüera-Gonzáles S, 2011, EUR J IMMUNOL, V41, P3667, DOI [10.1002/eji.20114165, 10.1002/eji.201141645]
[2]   Inflammation-Related Disorders in the Tryptophan Catabolite Pathway in Depression and Somatization [J].
Anderson, George ;
Maes, Michael ;
Berk, Michael .
INFLAMMATION IN NEUROPSYCHIATRIC DISORDERS, 2012, 88 :27-48
[3]   Role of the Xenobiotic Receptor in Inflammatory Bowel Disease [J].
Arsenescu, Razvan ;
Arsenescu, Violeta ;
Zhong, Jian ;
Nasser, Munira ;
Melinte, Razvan ;
Dingle, R. W. Cameron ;
Swanson, Hollie ;
de Villiers, Willem J. .
INFLAMMATORY BOWEL DISEASES, 2011, 17 (05) :1149-1162
[4]   MELATONIN AND 6-SULFATOXYMELATONIN CIRCADIAN-RHYTHMS IN SERUM AND URINE OF PRIMARY PROSTATE-CANCER PATIENTS - EVIDENCE FOR REDUCED PINEAL ACTIVITY AND RELEVANCE OF URINARY DETERMINATIONS [J].
BARTSCH, C ;
BARTSCH, H ;
SCHMIDT, A ;
ILG, S ;
BICHLER, KH ;
FLUCHTER, SH .
CLINICA CHIMICA ACTA, 1992, 209 (03) :153-167
[5]   Circadian Modulation of Gene Expression, but not Glutamate Uptake, in Mouse and Rat Cortical Astrocytes [J].
Beaule, Christian ;
Swanstrom, Adrienne ;
Leone, Maria Juliana ;
Herzog, Erik D. .
PLOS ONE, 2009, 4 (10)
[6]   Role of Epigenetic Mechanisms in Differential Regulation of the Dioxin-Inducible Human CYP1A1 and CYP1B1 Genes [J].
Beedanagari, Sudheer R. ;
Taylor, Robert T. ;
Bui, Peter ;
Wang, Feng ;
Nickerson, Derek W. ;
Hankinson, Oliver .
MOLECULAR PHARMACOLOGY, 2010, 78 (04) :608-616
[7]   The aryl hydrocarbon receptor complex and the control of gene expression [J].
Beischlag, Timothy V. ;
Morales, J. Luis ;
Hollingshead, Brett D. ;
Perdew, Gary H. .
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 2008, 18 (03) :207-250
[8]   ERα-AHR-ARNT protein-protein interactions mediate estradiol-dependent transrepression of dioxin-inducible gene transcription [J].
Beischlag, TV ;
Perdew, GH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (22) :21607-21611
[9]   Recruitment of the NCoA/SRC-1/p160 family of transcriptional coactivators by the aryl hydrocarbon receptor/aryl hydrocarbon receptor nuclear translocator complex [J].
Beischlag, TV ;
Wang, S ;
Rose, DW ;
Torchia, J ;
Reisz-Porszasz, S ;
Muhammad, K ;
Nelson, WE ;
Probst, MR ;
Rosenfeld, MG ;
Hankinson, O .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (12) :4319-4333
[10]   The RelB subunit of NFκB acts as a negative regulator of circadian gene expression [J].
Bellet, Marina M. ;
Zocchi, Loredana ;
Sassone-Corsi, Paolo .
CELL CYCLE, 2012, 11 (17) :3304-3311