MicroRNA-221 controls expression of intercellular adhesion molecule-1 in epithelial cells in response to Cryptosporidium parvum infection

被引:32
作者
Gong, Ai-Yu [1 ]
Hu, Guoku [1 ]
Zhou, Rui [1 ]
Liu, Jun [1 ]
Feng, Yaoyu [2 ]
Soukup, Garrett A. [3 ]
Chen, Xian-Ming [1 ]
机构
[1] Creighton Univ, Med Ctr, Dept Med Microbiol & Immunol, Omaha, NE 68178 USA
[2] E China Univ Sci & Technol, Sch Resources & Environm Engn, Shanghai 200237, Peoples R China
[3] Creighton Univ, Med Ctr, Dept Biomed Sci, Omaha, NE 68178 USA
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
Epithelial cells; MicroRNAs; Cryptosporidium parvum; ICAM-1; Lymphocytes; Adhesion molecules; Inflammation; NECROSIS-FACTOR-ALPHA; HUMAN CHOLANGIOCYTES; ICAM-1; EXPRESSION; IMMUNE-RESPONSES; MICE; RNA; BIOGENESIS; CYTOKINE; LINES;
D O I
10.1016/j.ijpara.2010.11.011
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Cryptosporidium parvum is a protozoan parasite that infects gastrointestinal epithelial cells and causes diarrhoeal disease in humans and animals globally. Pathological changes following C parvum infection include crypt hyperplasia and a modest inflammatory reaction with increased infiltration of lymphocytes into intestinal mucosa. Expression of adhesion molecules, such as intercellular adhesion molecule-1 (ICAM-1), on infected epithelial cell surfaces may facilitate adhesion and recognition of lymphocytes at infection sites. MicroRNAs (miRNAs) are small RNA molecules of 23 nucleotides that negatively regulate protein-coding gene expression via translational suppression or mRNA degradation. We recently reported that microRNA-221 (miR-221) regulates ICAM-1 translation through targeting the ICAM-1 3'-untranslated region (UTR). In this study, we tested the role of miR-221 in regulating ICAM-1 expression in epithelial cells in response to C parvum infection using an in vitro model of human biliary cryptosporidiosis. Up-regulation of ICAM-1 at both message and protein levels was detected in epithelial cells following C. parvum infection. Inhibition of ICAM-1 transcription with actinomycin D could only partially block C. parvum-induced ICAM-1 expression at the protein level. Cryptosporidium parvum infection decreased miR-221 expression in infected epithelial cells. When cells were transfected with a luciferase reporter construct covering the miR-221 binding site in the ICAM-1 3'-UTR and then exposed to C. parvum, an enhanced luciferase activity was detected. Transfection of miR-221 precursor abolished C. parvum-stimulated ICAM-1 protein expression. In addition, expression of ICAM-1 on infected epithelial cells facilitated epithelial adherence of co-cultured Jurkat cells. These results indicate that miR-221-mediated translational suppression controls ICAM-1 expression in epithelial cells in response to C. parvum infection. (C) 2011 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:397 / 403
页数:7
相关论文
共 33 条
[1]   Cryptosporidium parvum Infection Rapidly Induces a Protective Innate Immune Response Involving Type I Interferon [J].
Barakat, Farah M. ;
McDonald, Vincent ;
Foster, Graham R. ;
Tovey, Michael G. ;
Korbel, Daniel S. .
JOURNAL OF INFECTIOUS DISEASES, 2009, 200 (10) :1548-1555
[2]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[3]   A cellular Micro-RNA, let-7i, regulates toll-like receptor 4 expression and contributes to cholangiocyte immune responses against Cryptosporidium parvum infection [J].
Chen, Xian-Ming ;
Splinter, Patrick L. ;
O'Hara, Steven P. ;
LaRusso, Nicholas F. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (39) :28929-28938
[4]   Multiple TLRs are expressed in human cholangiocytes and mediate host epithelial defense responses to Cryptosporidium parvum via activation of NF-κB [J].
Chen, XM ;
O'Hara, SP ;
Nelson, JB ;
Splinter, PL ;
Small, AJ ;
Tietz, PS ;
Limper, AH ;
LaRusso, NF .
JOURNAL OF IMMUNOLOGY, 2005, 175 (11) :7447-7456
[5]   Current concepts: Cryptosporidiosis [J].
Chen, XM ;
Keithly, JS ;
Paya, CV ;
LaRusso, NF .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (22) :1723-1731
[6]   The 3′ untranslated region of messenger RNA:: A molecular 'hotspot' for pathology? [J].
Conne, B ;
Stutz, A ;
Vassalli, JD .
NATURE MEDICINE, 2000, 6 (06) :637-641
[7]   Host intestinal epithelial response to Cryptosporidium parvum [J].
Deng, MQ ;
Rutherford, MS ;
Abrahamsen, MS .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (06) :869-884
[8]   Mucosal cytokine and antigen-specific responses to Cryptosporidium parvum in IL-12p40 KO mice [J].
Ehigiator, HN ;
Romagnoli, P ;
Borgelt, K ;
Fernandez, M ;
McNair, N ;
Secor, WE ;
Mead, JR .
PARASITE IMMUNOLOGY, 2005, 27 (1-2) :17-28
[9]   Haemophilus influenzae stimulates ICAM-1 expression on respiratory epithelial cells [J].
Frick, AG ;
Joseph, TD ;
Pang, LY ;
Rabe, AM ;
St Geme, JW ;
Look, DC .
JOURNAL OF IMMUNOLOGY, 2000, 164 (08) :4185-4196
[10]   Cryptosporidium parvum Induces B7-H1 Expression in Cholangiocytes by Down-Regulating MicroRNA-513 [J].
Gong, Ai-Yu ;
Zhou, Rui ;
Hu, Guoku ;
Liu, Jun ;
Sosnowska, Danuta ;
Drescher, Kristen M. ;
Dong, Haidong ;
Chen, Xian-Ming .
JOURNAL OF INFECTIOUS DISEASES, 2010, 201 (01) :160-169