Comparative proteome analysis of untreated and Helicobacter pylori-treated HepG2

To investigate the pathological effect of Helicobacter pylori (H pylori) on human hepatic cells, proteomic methods were used to find and to identify proteins that were overexpressed in HepG2 cells treated by H pylori. H pylori was co-cultured with HepG2 for 6 h. Two-dimensional gel electrophoresis w...

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Published inWorld journal of gastroenterology : WJG Vol. 11; no. 22; pp. 3485 - 3489
Main Authors Zhang, Yan, Fan, Xue-Gong, Chen, Ren, Xiao, Zhi-Qiang, Feng, Xue-Ping, Tian, Xue-Fei, Chen, Zhao-Hui
Format Journal Article
LanguageEnglish
Published United States Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China%Medical Research Center, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China 14.06.2005
Baishideng Publishing Group Inc
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Summary:To investigate the pathological effect of Helicobacter pylori (H pylori) on human hepatic cells, proteomic methods were used to find and to identify proteins that were overexpressed in HepG2 cells treated by H pylori. H pylori was co-cultured with HepG2 for 6 h. Two-dimensional gel electrophoresis was used to gain the protein expression pattern of untreated and H pylori-treated HepG2. After staining and image analysis, spots of interest were isolated and subjected to mass spectrometry. Seven proteins, which were up-regulated in H pylori-treated HepG2 cells, were identified. These proteins included integrin beta-1, protein kinase C alpha, LIM/homeobox protein Lhx1, eIF-2-beta, MAP kinase kinase 3, PINCH protein and Ras-related protein Rab-37, which involved in transcription regulation, signal transduction, metabolism and so on. H pylori may exert the pathological effect on HepG2 cells by up-regulating the expression of some proteins.
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Correspondence to: Xue-Gong Fan, Department of Infectious Diseases, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China. xgfan@hotmail.com
Author contributions: All authors contributed equally to the work.
Telephone: +86-731-4327392 Fax: +86-731-4327332
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.v11.i22.3485