Abstract | BACKGROUND: METHODS: In this study, immunolocalization of C. sinensis cathepsin B proteases (CsCBs) in C. sinensis worms was investigated. Four CsCBs were expressed in Pichia pastoris yeast cells. Purified yCsCBs were measured for enzymatic and hydrolase activities in the presence of various host proteins. Cell proliferation, wound-healing and transwell assays were performed to show the effect of CsCBs on human cells. RESULTS: CsCBs were localized in the excretory vesicle, oral sucker and intestinal tract of C. sinensis. Recombinant yCsCBs from yeast showed active enzymatic activity at pH 5.0-5.5 and at 37-42 °C. yCsCBs can degrade various host proteins including human serum albumin, human fibronectin, human hemoglobin and human IgG. CsCBs were detected in liver tissues of mice and cancer patients afflicted with clonorchiasis. Various bioassays collectively demonstrated that CsCBs could promote cell proliferation, migration and invasion of human cancer cells. CONCLUSION: Our results demonstrated that CsCBs can degrade various human proteins and we proved that the secreted CsCBs are involved in the pathogenesis of clonorchiasis.
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Authors | Wenjun Chen, Dan Ning, Xiaoyun Wang, Tingjin Chen, Xiaoli Lv, Jiufeng Sun, De Wu, Yan Huang, Jin Xu, Xinbing Yu |
Journal | Parasites & vectors
(Parasit Vectors)
Vol. 8
Pg. 647
(Dec 21 2015)
ISSN: 1756-3305 [Electronic] England |
PMID | 26691339
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Recombinant Proteins
- Virulence Factors
- Cathepsin B
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Topics |
- Animals
- Cathepsin B
(chemistry, genetics, isolation & purification, metabolism)
- Cell Proliferation
- Cloning, Molecular
- Clonorchiasis
(parasitology)
- Clonorchis sinensis
(enzymology, pathogenicity)
- Disease Models, Animal
- Enzyme Stability
- Gene Expression
- Humans
- Hydrogen-Ion Concentration
- Liver
(pathology)
- Mice
- Pichia
(genetics, metabolism)
- Proteolysis
- Recombinant Proteins
(chemistry, genetics, isolation & purification, metabolism)
- Temperature
- Virulence Factors
(chemistry, genetics, isolation & purification, metabolism)
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