The Role of Peroxiredoxins in the Regulation of Sepsis

被引:11
作者
Aki, Toshihiko [1 ]
Unuma, Kana [1 ]
Uemura, Koichi [1 ]
机构
[1] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Forens Med, Tokyo 1138519, Japan
关键词
peroxiredoxins; sepsis; inflammasome; pyroptosis; inflammation; OXIDATIVE STRESS; CRYSTAL-STRUCTURE; SEPTIC SHOCK; MITOCHONDRIAL DYSFUNCTION; INFLAMMASOME ACTIVATION; EXTRACELLULAR VESICLES; BACTERIAL FLAGELLIN; 2-CYS PEROXIREDOXIN; CUTTING EDGE; CELL DEATH;
D O I
10.3390/antiox11010126
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
Oxidative stress, a result of a disturbance in redox homeostasis, is considered to be one of the main aggravating events in the pathogenesis of immune disorders. Peroxiredoxins (Prdxs) are an enzyme family that catalyzes the reduction of peroxides, including hydrogen peroxide, lipid peroxides, and nitrogen peroxides. Although the maintenance of cellular redox homeostasis through Prdxs is essential for surviving in adverse environments, Prdxs also participate in the regulation of cellular signal transduction by modulating the activities of a panel of molecules involved in the signal transduction process. Although Prdxs were discovered as intracellular anti-oxidative enzymes, recent research has revealed that Prdxs also play important roles in the extracellular milieu. Indeed, Prdxs have been shown to have the capacity to activate immune cells through ligation with innate immune receptors such as toll-like receptors (TLRs). In this review, we will summarize the intracellular as well as extracellular roles of Prdxs for and against the pathogenesis of inflammatory disorders including sepsis, hemorrhagic shock, and drug-induced liver injury.
引用
收藏
页数:15
相关论文
共 105 条
[1]   GsdmD p30 elicited by caspase-11 during pyroptosis forms pores in membranes [J].
Aglietti, Robin A. ;
Estevez, Alberto ;
Gupta, Aaron ;
Ramirez, Monica Gonzalez ;
Liu, Peter S. ;
Kayagaki, Nobuhiko ;
Ciferri, Claudio ;
Dixit, Vishva M. ;
Dueber, Erin C. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (28) :7858-7863
[2]   The structure of reduced tryparedoxin peroxidase reveals a decamer and insight into reactivity of 2Cys-peroxiredoxins [J].
Alphey, MS ;
Bond, CS ;
Tetaud, E ;
Fairlamb, AH ;
Hunter, WN .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 300 (04) :903-916
[3]   Severe Sepsis and Septic Shock REPLY [J].
Angus, Derek C. ;
van der Poll, Tom .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 369 (21) :2063-2063
[4]   Cellular and Exosomal Regulations of Sepsis-Induced Metabolic Alterations [J].
Appiah, Michael G. ;
Park, Eun Jeong ;
Akama, Yuichi ;
Nakamori, Yuki ;
Kawamoto, Eiji ;
Gaowa, Arong ;
Shimaoka, Motomu .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (15)
[5]   Pyroptosis: host cell death and inflammation [J].
Bergsbaken, Tessa ;
Fink, Susan L. ;
Cookson, Brad T. .
NATURE REVIEWS MICROBIOLOGY, 2009, 7 (02) :99-109
[6]   Intracerebral Hemorrhage-Induced Brain Injury in Rats: the Role of Extracellular Peroxiredoxin 2 [J].
Bian, Liheng ;
Zhang, Jingwei ;
Wang, Ming ;
Keep, Richard F. ;
Xi, Guohua ;
Hua, Ya .
TRANSLATIONAL STROKE RESEARCH, 2020, 11 (02) :288-295
[7]   Peroxiredoxins wear many hats: Factors that fashion their peroxide sensing personalities [J].
Bolduc, Jesalyn ;
Koruza, Katarina ;
Luo, Ting ;
Pueyo, Julia Malo ;
Trung Nghia Vo ;
Ezerina, Daria ;
Messens, Joris .
REDOX BIOLOGY, 2021, 42
[8]   THE ACCP-SCCM CONSENSUS CONFERENCE ON SEPSIS AND ORGAN FAILURE [J].
BONE, RC ;
SIBBALD, WJ ;
SPRUNG, CL .
CHEST, 1992, 101 (06) :1481-1482
[9]   Glutathione peroxidases [J].
Brigelius-Flohe, Regina ;
Maiorino, Matilde .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2013, 1830 (05) :3289-3303
[10]   Lysosomal Exocytosis, Exosome Release and Secretory Autophagy: The Autophagic- and Endo-Lysosomal Systems Go Extracellular [J].
Buratta, Sandra ;
Tancini, Brunella ;
Sagini, Krizia ;
Delo, Federica ;
Chiaradia, Elisabetta ;
Urbanelli, Lorena ;
Emiliani, Carla .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (07)