Modulation of Inflammation and Immune Responses by Heme Oxygenase-1: Implications for Infection with Intracellular Pathogens

被引:28
作者
Costa, Diego L. [1 ]
Amaral, Eduardo P. [2 ]
Andrade, Bruno B. [3 ,4 ,5 ,6 ,7 ,8 ,9 ]
Sher, Alan [2 ]
机构
[1] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Bioquim & Imunol, BR-14049900 Ribeirao Preto, SP, Brazil
[2] NIAID, Immunobiol Sect, Lab Parasit Dis, NIH, Bethesda, MD 20892 USA
[3] Univ Cape Town, Wellcome Ctr Infect Dis Res Africa, Inst Infect Dis & Mol Med, ZA-7925 Cape Town, South Africa
[4] Fundacao Oswaldo Cruz, Inst Goncalo Moniz, BR-40296710 Salvador, BA, Brazil
[5] Multinatl Org Network Sponsoring Translat & Epide, BR-40210320 Salvador, BA, Brazil
[6] Fac Tecnol & Ciencias UniFTC, Curso Med, BR-41741590 Salvador, BA, Brazil
[7] Univ Salvador UNIFACS, Laureate Int Univ, Curso Med, BR-41770235 Salvador, BA, Brazil
[8] Escola Bahiana Med & Saude Publ EBMSP, BR-40290000 Salvador, BA, Brazil
[9] Vanderbilt Univ, Dept Med, Div Infect Dis, Sch Med, Nashville, TN 37232 USA
基金
巴西圣保罗研究基金会;
关键词
heme oxygenase-1; inflammation; immune response; infectious disease; intracellular pathogens; host directed therapy; NITRIC-OXIDE SYNTHASE; NF-KAPPA-B; 32-KDA STRESS PROTEIN; CARBON-MONOXIDE; TRANSCRIPTIONAL ACTIVATION; BILIVERDIN REDUCTASE; OXIDATIVE STRESS; IRON HOMEOSTASIS; NUCLEAR TRANSLOCATION; GENE-EXPRESSION;
D O I
10.3390/antiox9121205
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
Heme oxygenase-1 (HO-1) catalyzes the degradation of heme molecules releasing equimolar amounts of biliverdin, iron and carbon monoxide. Its expression is induced in response to stress signals such as reactive oxygen species and inflammatory mediators with antioxidant, anti-inflammatory and immunosuppressive consequences for the host. Interestingly, several intracellular pathogens responsible for major human diseases have been shown to be powerful inducers of HO-1 expression in both host cells and in vivo. Studies have shown that this HO-1 response can be either host detrimental by impairing pathogen control or host beneficial by limiting infection induced inflammation and tissue pathology. These properties make HO-1 an attractive target for host-directed therapy (HDT) of the diseases in question, many of which have been difficult to control using conventional antibiotic approaches. Here we review the mechanisms by which HO-1 expression is induced and how the enzyme regulates inflammatory and immune responses during infection with a number of different intracellular bacterial and protozoan pathogens highlighting mechanistic commonalities and differences with the goal of identifying targets for disease intervention.
引用
收藏
页码:1 / 30
页数:30
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