Proteomic Analysis of Differentially Expressed Proteins in Human Cholangiocarcinoma Cells Treated with Clonorchis sinensis Excretory-Secretory Products

被引:46
作者
Pak, Jhang Ho [1 ]
Moon, Ju Hyun [1 ]
Hwang, Seung-Jun [2 ]
Cho, Shin-Hyeong [3 ]
Seo, Sang-Beom [4 ]
Kim, Tong-Soo [5 ]
机构
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Asan Inst Life Sci, Seoul 138736, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Anat & Cell Biol, Seoul 138736, South Korea
[3] Natl Inst Hlth, Div Malaria & Parasit Dis, Seoul 122701, South Korea
[4] Chung Ang Univ, Coll Nat Sci, Dept Life Sci, Seoul 156756, South Korea
[5] Inha Univ, Sch Med, Dept Parasitol, Inchon 400103, South Korea
关键词
Clonorchis sinensis; EXCRETORY-SECRETORY PRODUCTS; HUMAN CHOLANGIOCARCINOMA CELLS (HuCCT1); PEROXIREDOXIN; 2-DE-BASED PROTEOMICS; GLUTATHIONE-S-TRANSFERASE; FASCIOLA-HEPATICA; SERODIAGNOSTIC ANTIGEN; OPISTHORCHIS-VIVERRINI; PEROXIREDOXIN-VI; PROFILE CHANGES; CANCER; IDENTIFICATION; PROLIFERATION; PROGRESSION;
D O I
10.1002/jcb.22368
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
Severe Clonorchis sinensis infection is a significant risk factor for malignant changes in bile ducts and surrounding liver tissues occurring as a result of direct contact with C. sinensis worms and their excretory-secretory products (ESP). However, the intrinsic molecular mechanisms involved in these processes remain obscure. To determine the effects or C. sinensis infection on protein expression in host bile duct epithelium, we examined proteomic profile changes in the human cholangiocarcinoma cell line (HuCCT1) treated with ESP at 24 h. Using a combination of 2-DE, quantitative image and MALDI-TOF MS analysis, we identified 83 proteins that were translationally modulated in response to ESP, among which 49 were up-regulated and 34 down-regulated. These proteins were classified under various biological categories, including metabolism, cell structure and architecture, proteolysis, protein modification, transport, signal transduction, and reactive oxygen species (ROS) detoxification. In particular, ESP induced the expression of redox-regulating proteins, including peroxiredoxins (Prdx 2, 3, and 6) and thioredoxin 1 (Trx 1), possibly via intraccllular ROS generation. Application of the proteomic approach to identify ESP response proteins should be a prerequisite before further investigation to clarify the molecular pathways and mechanisms involved in C. sinensis infection of host cells. J. Cell. Biochem. 108: 1376-1388, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:1376 / 1388
页数:13
相关论文
共 39 条
[1]   Proteomics: quantitative and physical mapping of cellular proteins [J].
Blackstock, WP ;
Weir, MP .
TRENDS IN BIOTECHNOLOGY, 1999, 17 (03) :121-127
[2]   Inhibition of spleen cell proliferative response to mitogens by excretory-secretory antigens of Fasciola hepatica [J].
Cervi, L ;
Masih, DT .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 1997, 27 (05) :573-579
[3]   Identification of the functional role of peroxiredoxin 6 in the progression of breast cancer [J].
Chang, Xin-Zhong ;
Li, Da-Qiang ;
Hou, Yi-Feng ;
Wu, Jiong ;
Lu, Jin-Song ;
Di, Gen-Hong ;
Jin, Wei ;
Ou, Zhou-Luo ;
Shen, Zhen-Zhou ;
Shao, Zhi-Ming .
BREAST CANCER RESEARCH, 2007, 9 (06)
[4]   Cholangiocarcinoma and Clonorchis sinensis infection:: A case-control study in Korea [J].
Choi, Dongil ;
Lim, Jae Hoon ;
Lee, Kyu Taek ;
Lee, Jong Kyun ;
Choi, Seong Ho ;
Heo, Jin Seok ;
Jang, Kee-Taek ;
Lee, Nam Yong ;
Kim, Seonwoo ;
Hong, Sung-Tae .
JOURNAL OF HEPATOLOGY, 2006, 44 (06) :1066-1073
[5]   How much human helminthiasis is there in the world? [J].
Crompton, DWT .
JOURNAL OF PARASITOLOGY, 1999, 85 (03) :397-403
[6]   Advances in our understanding of peroxiredoxin, a multifunctional, mammalian redox protein [J].
Fujii, J ;
Ikeda, Y .
REDOX REPORT, 2002, 7 (03) :123-130
[7]   Peroxiredoxins [J].
Hofmann, B ;
Hecht, HJ ;
Flohé, L .
BIOLOGICAL CHEMISTRY, 2002, 383 (3-4) :347-364
[8]   Clonorchis sinensis:: glutathione S-transferase as a serodiagnostic antigen for detecting IgG and IgE antibodies [J].
Hong, SJ ;
Kim, TY ;
Gan, XX ;
Shen, LY ;
Sukontason, K ;
Sukontason, K ;
Kang, SY .
EXPERIMENTAL PARASITOLOGY, 2002, 101 (04) :231-233
[9]   Peroxiredoxins, oxidative stress, and cell proliferation [J].
Immenschuh, S ;
Baumgart-Vogt, E .
ANTIOXIDANTS & REDOX SIGNALING, 2005, 7 (5-6) :768-777
[10]  
Jefferies JR, 2001, PROTEOMICS, V1, P1128, DOI 10.1002/1615-9861(200109)1:9<1128::AID-PROT1128>3.3.CO