Cell permeable NFAT inhibitory peptide Sim-2-VIVIT inhibits T-cell activation and alleviates allergic airway inflammation and hyper-responsiveness

被引:22
作者
Choi, Je-Min [1 ,2 ]
Sohn, Jung-Ho [1 ,2 ,3 ]
Park, Tae-Yoon [4 ,5 ]
Park, Jung-Won [3 ]
Lee, Sang-Kyou [4 ,5 ]
机构
[1] Hanyang Univ, Res Inst Nat Sci, Dept Life Sci, Seoul 133791, South Korea
[2] Hanyang Biomed Res Inst, Seoul 133791, South Korea
[3] Yonsei Med Sch, Div Allergy & Immunol, Dept Internal Med, Seoul 120749, South Korea
[4] Yonsei Univ, Coll Life Sci & Biotechnol, Dept Biotechnol, Seoul 120749, South Korea
[5] Natl Creat Res Initiat Ctr Inflammatory Response, Seoul 120749, South Korea
基金
新加坡国家研究基金会;
关键词
NFAT; VIVIT; Cell permeable peptide; Asthma; TAT-FUSION PROTEINS; CYCLOSPORINE-A; DELIVERY; TRANSDUCTION; CALCINEURIN; ASTHMA; TRANSPLANTATION; INTERNALIZATION; NEPHROTOXICITY; DOMAIN;
D O I
10.1016/j.imlet.2012.01.016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nuclear factor of activated T cells (NFAT) is an important transcription factor for the production of interleukin (IL)-2 upon T-cell receptor (TcR) signaling. Therefore, inhibition of the NFAT-carcineurin pathway is an important target for inflammatory disease inhibition and graft rejection. A novel cell permeable peptide (CPP), Sim-2, has been identified from a human transcription factor, and Sim-2-CPP conjugated to beta-galactosidase or EGFP protein was efficiently delivered into cells in vitro and in vivo. A cell permeable form of the NFAT inhibitory peptide VIVIT (Sim-2-VIVIT) was synthesized and showed inhibitory effects on human CD4 or CD8 T-cell activation through NFAT transcriptional activity suppression and IL-2 inhibition. Intranasal administration of the Sim-2-VIVIT peptide in an ovalbumin (OVA)-induced murine asthma model alleviated peribronchial and perivascular infiltration of inflammatory cells in the lung and caused airway remodeling and airway hyper-responsiveness. These results suggest that cell permeable Sim-2-VIVIT peptide has clinical potential as an immunosuppressive agent for inflammatory diseases. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:170 / 176
页数:7
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