Molecular and physiological roles of Pellino E3 ubiquitin ligases in immunity

被引:30
作者
Humphries, Fiachra [1 ]
Moynagh, Paul N. [1 ,2 ]
机构
[1] Natl Univ Ireland Maynooth, Dept Biol, Inst Immunol, Maynooth, Kildare, Ireland
[2] Queens Univ Belfast, Sch Med Dent & Biomed Sci, Ctr Infect & Immun, Belfast BT7 1NN, Antrim, North Ireland
基金
爱尔兰科学基金会;
关键词
Pellino E3 ubiquitin ligases; innate immunity; Toll-like receptors; NOD-like receptors; inflammation; ubiquitination; NF-KAPPA-B; TOLL-LIKE RECEPTOR; NOD-LIKE RECEPTORS; CELL-DEATH; FHA DOMAIN; INTERFERON-PRODUCTION; INSULIN-RESISTANCE; ADAPTER PROTEIN; INNATE IMMUNITY; CUTTING EDGE;
D O I
10.1111/imr.12306
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The sensing of foreign agents by the innate and adaptive immune system triggers complex signal transduction cascades that culminate in expression of gene patterns that facilitate host protection from the invading agent. Post-translational modification of intracellular signaling proteins in these pathways is a key regulatory mechanism with ubiquitination being one of the important processes that controls levels and activities of signaling molecules. E3 ubiquitin ligases are the determining enzymes in dictating the ubiquitination status of individual proteins. Among these hundred E3 ubiquitin ligases are a family of Pellino proteins that are emerging to be important players in immunity and beyond. Herein, we review the roles of the Pellino E3 ubiquitin ligases in innate and adaptive immunity. We discuss their early discovery and characterization and how this has been aided by the highly conserved nature of innate immune signaling across evolution. We describe the molecular roles of Pellino proteins in immune signaling with particular emphasis on their involvement in pathogen recognition receptor (PRR) signaling. The growing appreciation of the importance of Pellino proteins in a wide range of immune-mediated diseases are also evaluated.
引用
收藏
页码:93 / 108
页数:16
相关论文
共 126 条
[1]   Coordinated regulation of toll-like receptor and NOD2 signaling by k63-linked polyubiquitin chains [J].
Abbott, Derek W. ;
Yang, Yibin ;
Hutti, Jessica E. ;
Madhavarapu, Swetha ;
Kelliher, Michelle A. ;
Cantley, Lewis C. .
MOLECULAR AND CELLULAR BIOLOGY, 2007, 27 (17) :6012-6025
[2]   Signalling pathways of the TNF superfamily: A double-edged sword [J].
Aggarwal, BB .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (09) :745-756
[3]   Mediators of Neutrophil Function in Children With Protracted Bacterial Bronchitis [J].
Baines, Katherine J. ;
Upham, John W. ;
Yerkovich, Stephanie T. ;
Chang, Anne B. ;
Marchant, Julie M. ;
Carroll, Melanie ;
Simpson, Jodie L. ;
Gibson, Peter G. .
CHEST, 2014, 146 (04) :1013-1020
[4]   Novel immune genes associated with excessive inflammatory and antiviral responses to rhinovirus in COPD [J].
Baines, Katherine J. ;
Hsu, Alan C-Y ;
Tooze, Melinda ;
Gunawardhana, Lakshitha P. ;
Gibson, Peter G. ;
Wark, Peter A. B. .
RESPIRATORY RESEARCH, 2013, 14
[5]   Transcriptional phenotypes of asthma defined by gene expression profiling of induced sputum samples [J].
Baines, Katherine J. ;
Simpson, Jodie L. ;
Wood, Lisa G. ;
Scott, Rodney J. ;
Gibson, Peter G. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2011, 127 (01) :153-U251
[6]   NF-κB, Inflammation, and Metabolic Disease [J].
Baker, Rebecca G. ;
Hayden, Matthew S. ;
Ghosh, Sankar .
CELL METABOLISM, 2011, 13 (01) :11-22
[7]   A cell biological view of Toll-like receptor function: regulation through compartmentalization [J].
Barton, Gregory M. ;
Kagan, Jonathan C. .
NATURE REVIEWS IMMUNOLOGY, 2009, 9 (08) :535-542
[8]   BCL6: Master Regulator of the Germinal Center Reaction and Key Oncogene in B Cell Lymphomagenesis [J].
Basso, Katia ;
Dalla-Favera, Riccardo .
ADVANCES IN IMMUNOLOGY, VOL 105, 2010, 105 :193-210
[9]   Pellino-1 Selectively Regulates Epithelial Cell Responses to Rhinovirus [J].
Bennett, Julie A. ;
Prince, Lynne R. ;
Parker, Lisa C. ;
Stokes, Clare A. ;
de Bruin, Harold G. ;
van den Berge, Maarten ;
Heijink, Irene H. ;
Whyte, Moira K. ;
Sabroe, Ian .
JOURNAL OF VIROLOGY, 2012, 86 (12) :6595-6604
[10]   cIAP1 and cIAP2 facilitate cancer cell survival by functioning as E3 ligases that promote RIP1 ubiquitination [J].
Bertrand, Mathieu J. M. ;
Milutinovic, Snezana ;
Dickson, Kathleen M. ;
Ho, Wai Chi ;
Boudreault, Alain ;
Durkin, Jon ;
Gillard, John W. ;
Jaquith, James B. ;
Morris, Stephen J. ;
Barker, Philip A. .
MOLECULAR CELL, 2008, 30 (06) :689-700