Inhibitor of apoptosis proteins in human health and disease

被引:49
作者
Hrdinka, Matous [1 ,2 ]
Yabal, Monica [3 ]
机构
[1] Univ Hosp Ostrava, Dept Haematooncol, 17 Listopadu 1790, Ostrava 70800, Czech Republic
[2] Univ Ostrava, Fac Med, Syllabova 19, Ostrava 70300, Czech Republic
[3] Tech Univ Munich, Sch Med, Inst Mol Immunol & Expt Oncol, Ismaninger Str22, D-81675 Munich, Germany
关键词
X-LINKED INHIBITOR; NF-KAPPA-B; PERIODIC SYNDROME TRAPS; CELL-DEATH; XIAP DEFICIENCY; INFLAMMASOME ACTIVATION; CAUSES AUTOINFLAMMATION; NLRC4; CAUSES; UBIQUITIN; IAPS;
D O I
10.1038/s41435-019-0078-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The inhibitor of apoptosis proteins (IAPs) are best known for their ability to regulate cell survival and death processes. However, in addition to cell death, IAPs also act as innate immune sensors and modulate multiple pathways, such as autophagy and cell division. Many of these IAP functions are non-redundant even though they are based on the same molecular mechanism of action. These distinct functions of IAPs derive from their capacity to target specific substrates for ubiquitination and/or proteolytic cleavage. The unique functions of IAPs also derives from their unique cellular localizations, cell type and tissue-specific expression patterns. The diverse roles of IAPs are reflected by the fact that in humans the IAP family comprises eight distinct members. Genetic evidence from human pathologies also attests to the non-redundant functions of the IAPs since very diverse diseases arise upon aberrant IAP expression. In this review, we give an overview of the known mechanisms of action of the various IAPs, and focus on their specific roles in mediating innate immunity. We also look at the distinct phenotypes related to the dysregulation of the IAPs, and the human pathologies associated with each human IAP.
引用
收藏
页码:641 / 650
页数:10
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