Integrated stress response-altered pro-inflammatory signals in mucosal immune-related cells

被引:12
|
作者
Park, Seong-Hwan [1 ]
Moon, Yuseok [1 ,2 ]
机构
[1] Pusan Natl Univ, Sch Med, Dept Microbiol & Immunol, Lab Mucosal Exposome & Biomodulat, Yangsan 626870, South Korea
[2] Pusan Natl Univ, Res Inst Basic Sci, Pusan, South Korea
关键词
Integrated stress responses; luminal antigens; mucosal inflammation; ENDOPLASMIC-RETICULUM STRESS; NF-KAPPA-B; DOUBLE-STRANDED-RNA; ACTIVATED PROTEIN-KINASE; CCAAT/ENHANCER-BINDING PROTEIN; REGULATED EIF2-ALPHA KINASE; INITIATION FACTOR-2-ALPHA KINASE; RIBOSOME-INACTIVATING PROTEINS; ASPARAGINE SYNTHETASE GENE; AMINO-ACID DEPRIVATION;
D O I
10.3109/08923973.2012.742535
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Various cells are associated with the integrated stress response (ISR) that leads to translation arrest via phosphorylation of the alpha subunit of eukaryotic translation initiation factor 2. Pathogenic insults or nutritional imbalance in the mucosal tissues including the intestinal, airway, and genitourinary epithelia can cause ISRs, which have been linked to different mucosal inflammatory responses and subsequent systemic diseases. In particular, translational arrest caused by the early recognition of luminal microbes as well as nutritional status allows the human body to mount appropriate responses and maintain homeostasis both at the cellular and systemic levels. However, an over- or reduced ISR can create pathogenic conditions such as inflammation and carcinogenesis. This present review explores the association between eIF2 alpha kinase- linked pathways and mucosal or systemic proinflammatory signals activated by xenobiotic insults (such as ones caused by microbes or nutritional abnormalities). Understanding ISR-modulated cellular alterations will provide progressive insights into approaches for treating human mucosal inflammatory and metabolic disorders.
引用
收藏
页码:205 / 214
页数:10
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