Search

Copyright of International Architecture is the property of Omniscient Pte. Ltd. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Objective To construct the eukaryotic expression vectors of interleukin-12 (IL-12) and granulocyte-macrophage colony-stimulating factor (GM-CSF), PBI-CMV3-IL-12 and PBI-CMV3-GM-CSF, and the expression of IL-12 and GM-CSF in hepatoma cells after H22 hepatoma cells are transfected with such vectors. Methods The Trizol method was used to extract total liver RNA from mice, which was then reversely transcribed into cDNA. The coding sequences of IL-12 and GM-CSF were obtained by amplification using specific primers containing BamHI and HindIII restriction sites. Double enzyme digestion was performed for the products and PBI-CMV3 empty vectors, and then the digested products were transformed into DH5α after being recycled by gel extraction kit and connected by T4 DNA ligase. Monoclonal bacterial colonies were selected and plasmid extraction, enzyme digestion, and DNA sequencing were performed for the identification of the expression vector constructed. The constructed plasmids were divided into empty vector group, PBI-CMV3-IL-12 group, PBI-CMV3-GM-CSF group, and co-transfection group. These plasmids were transfected into H22 hepatoma cells, and quantitative real-time PCR and Western blot were used to measure the mRNA and protein expression of IL-12 and GM-CSF in cells. A one-way analysis of variance was used for comparison of continuous data between multiple groups, and the Dunnett′s T3 method was used for further comparison between two groups. Results The eukaryotic expression vectors, PBI-CMV3-IL-12 and PBI-CMV3-GM-CSF, were successfully constructed. Quantitative real-time PCR showed that there were significant differences in the mRNA expression of IL-12 and GM-CSF between the four groups (F=522 and 163, both P＜0.001). Compared with the empty vector group, the PBI-CMV3-IL-12 group and the co-transfection group had a significant increase in the mRNA expression of IL-12 (both P＜0.05). Compared with the empty vector group, the PBI-CMV3-GM-CSF group and the co-transfection group had a significant increase in the mRNA expression of GM-CSF (both P＜0.05). Western blot showed that the interest protein could bind to antibody and produce a specific band in the membrane, and an analysis of band size and gray value showed that the protein expression of IL-12 and GM-CSF had a similar trend as the mRNA expression of IL-12 and GM-CSF. Conclusion The eukaryotic expression vectors of IL-12 and GM-CSF are successfully constructed, and they are highly expressed in H22 hepatoma cells. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Clinical Hepatology / Linchuang Gandanbing Zazhi is the property of Journal of Clinical Hepatology and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The incidence of nonalcoholic fatty liver disease (NAFLD) has been increasing in China year by year, and NAFLD has become the second most common liver disease after viral hepatitis. Its development is closely associated with insulin resistance and oxidative stress and NAFLD is one of the important components of metabolic syndrome. Ghrelin is a newly discovered endogenous ligand for growth hormone secretagogue and has broad biological functions. Ghrelin not only affects the metabolic process of glucose and lipids, but also plays an important role in the development and progression of NAFLD. In this review, the role of endogenous Ghrelin expression in the development and progression of NAFLD is briefly summarized and the Ghrelin regulation in the development and progression of NAFLD is pointed out, which will provide new approaches to the clinical treatment of NAFLD. [ABSTRACT FROM AUTHOR]