Molecular characterization and immunological roles of avian IL-22 and its soluble receptor IL-22 binding protein

被引:22
|
作者
Kim, Sungwon [1 ]
Faris, Laura [1 ]
Cox, Chasity M. [1 ]
Sumners, Lindsay H. [1 ]
Jenkins, Mark C. [2 ]
Fetterer, Ray H. [2 ]
Miska, Kate B. [3 ]
Dalloul, Rami A. [1 ]
机构
[1] Virginia Tech, Dept Anim & Poultry Sci, Avian Immunobiol Lab, Blacksburg, VA 24061 USA
[2] ARS, Anim Parasit Dis Lab, USDA, Beltsville, MD 20705 USA
[3] ARS, Anim Biosci & Biotechnol Lab, USDA, Beltsville, MD 20705 USA
关键词
Chicken; IL-10; IL-22; IL22BP; Inflammation; INDUCIBLE FACTOR; INTERLEUKIN; 22; FUNCTIONAL-CHARACTERIZATION; HOST-DEFENSE; IL-TIF; CLONING; CYTOKINE; CELLS; IDENTIFICATION; IL-10;
D O I
10.1016/j.cyto.2012.08.005
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
As a member of the interleukin (IL)-10 family, IL-22 is an important mediator in modulating tissue responses during inflammation. Through activation of STAT3-signaling cascades, IL-22 induces proliferative and anti-apoptotic pathways, as well as antimicrobial peptides (AMPS), that help prevent tissue damage and aid in its repair. This study reports the cloning and expression of recombinant chicken IL-22 (rChIL-22) and its soluble receptor, rChIL22BP, and characterization of biological effects of rChIL-22 during inflammatory responses. Similar to observations with mammalian IL-22, purified rChIL-22 had no effect on either peripheral blood mononuclear cells (PBMCs) or lymphocytes. This was due to the low expression of the receptor ChIL22RA1 chain compared to ChIL10RB chain. rChIL-22 alone did not affect chicken embryo kidney cells (CEKCs); however, co-stimulation of CEKCs with LPS and rChIL-22 enhanced the production of pro-inflammatory cytokines, chemokines and AMPs. Furthermore, rChIL-22 alone stimulated and induced acute phase reactants in chicken embryo liver cells (CELCs). These effects of rChIL-22 were abolished by pre-incubation of rChIL-22 with rChIL22BP. Together, this study indicates an important role of ChIL-22 on epithelial cells and hepatocytes during inflammation. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:815 / 827
页数:13
相关论文
共 50 条
  • [1] IL-22 and IL-22 binding protein in atopic dermatitis
    Varandas, C.
    Lopes, A.
    Neto, M.
    Duarte, F.
    Fernandes, N.
    Paulino, M.
    Coutinho, C.
    Mendes, A.
    Cosme, J.
    Caiado, J.
    Costa, C.
    Spinola, A.
    Branco Ferreira, M.
    Lopes Da Silva, S.
    Pereira Santos, M. C.
    ALLERGY, 2021, 76 : 221 - 222
  • [2] THE IL-22 BINDING PROTEIN ISOFORMS ARE A RHEOSTAT FOR IL-22 SIGNALING
    Lim, C.
    Hong, M.
    Savan, R.
    CYTOKINE, 2016, 87 : 73 - 73
  • [3] IL-22 Binding Protein (IL-22BP) in the Regulation of IL-22 Biology
    Zenewicz, Lauren A.
    FRONTIERS IN IMMUNOLOGY, 2021, 12
  • [4] IL-22 Binding Protein/IL-22 Axis in Regulating Acute Lung Injury
    Pillar, Amber
    Ali, Md Khadem
    AMERICAN JOURNAL OF PATHOLOGY, 2024, 194 (03): : 335 - 337
  • [5] The human IL-22 binding protein isoforms are a rheostat for IL-22 signaling.
    Lim, Chrissie
    Hong, Meeae
    Savan, Ram
    JOURNAL OF IMMUNOLOGY, 2016, 196
  • [6] Human IL-22 binding protein isoforms act as a rheostat for IL-22 signaling
    Lim, Chrissie
    Hong, MeeAe
    Savan, Ram
    SCIENCE SIGNALING, 2016, 9 (447)
  • [7] Cloning and characterization of mouse IL-22 binding protein
    Wei, CC
    Ho, TW
    Liang, WG
    Chen, GY
    Chang, MS
    GENES AND IMMUNITY, 2003, 4 (03) : 204 - 211
  • [8] Cloning and characterization of mouse IL-22 binding protein
    Chi-Chen Wei
    T-W Ho
    W-G Liang
    G-Y Chen
    Ming-Shi Chang
    Genes & Immunity, 2003, 4 : 204 - 211
  • [9] Il-22 / Il-22 Binding Protein (il-22ra2) Balance Is Critical For The Resolution Of Influenza Induced Lung Pathology
    Pociask, D.
    Kolls, J.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2016, 193
  • [10] IL-22 and IL-22 Binding Protein (IL-22BP) Regulate Fibrosis and Cirrhosis in Hepatitis C Virus and Schistosome Infections
    Sertorio, Mathieu
    Hou, Xunya
    Carmo, Rodrigo F.
    Dessein, Helia
    Cabantous, Sandrine
    Abdelwahed, Mohammed
    Romano, Audrey
    Albuquerque, Fernanda
    Vasconcelos, Luydson
    Carmo, Theomira
    Li, Jun
    Varoquaux, Arthur
    Arnaud, Violaine
    Oliveira, Pablo
    Hamdoun, Anas
    He, Hongbin
    Adbelmaboud, Suzan
    Mergani, Adil
    Zhou, Jie
    Monis, Ahmed
    Pereira, Leila Beltrao
    Halfon, Philippe
    Bourliere, Marc
    Parana, Raymundo
    dos Reis, Mitermayer
    Gonnelli, David
    Moura, Patricia
    Elwali, Nasr Eldin
    Argiro, Laurent
    Li, Yuesheng
    Dessein, Alain
    HEPATOLOGY, 2015, 61 (04) : 1321 - 1331