RNA Interference against Discoidin Domain Receptor 2 Ameliorates Alcoholic Liver Disease in Rats
Discoidin domain receptor 2 (DDR2) is involved in fibrotic disease. However, the exact pathogenic implications of the receptor in early alcoholic liver disease are still controversial. We constructed plasmid vectors encoding short-hairpin RNA against DDR2 to investigate its role in alcoholic liver d...
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Published in | PloS one Vol. 8; no. 2; p. e55860 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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07.02.2013
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Abstract | Discoidin domain receptor 2 (DDR2) is involved in fibrotic disease. However, the exact pathogenic implications of the receptor in early alcoholic liver disease are still controversial. We constructed plasmid vectors encoding short-hairpin RNA against DDR2 to investigate its role in alcoholic liver disease in an immortalized rat hepatic stellate cell line, HSC-T6, and in rats by MTT, RT-PCR and western blot analyses; immunohistochemistry and electron microscopy. Alcohol-induced upregulation of DDR2 was associated with the expression of matrix metalloproteinase 2, the transforming growth factor β1 signaling pathway and tissue inhibitor of metalloproteinase 1; collagen deposition; and extracellular matrix remodeling. Inhibition of DDR2 decreased HSC-T6 cell proliferation and liver injury in rats with 10-week-induced alcoholic liver disease. DDR2 may have an important role in the pathogenesis of early-stage alcoholic liver disease. Silencing DDR2 may be effective in preventing early-stage alcoholic liver disease. |
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AbstractList | Discoidin domain receptor 2 (DDR2) is involved in fibrotic disease. However, the exact pathogenic implications of the receptor in early alcoholic liver disease are still controversial. We constructed plasmid vectors encoding short-hairpin RNA against DDR2 to investigate its role in alcoholic liver disease in an immortalized rat hepatic stellate cell line, HSC-T6, and in rats by MTT, RT-PCR and western blot analyses; immunohistochemistry and electron microscopy. Alcohol-induced upregulation of DDR2 was associated with the expression of matrix metalloproteinase 2, the transforming growth factor β1 signaling pathway and tissue inhibitor of metalloproteinase 1; collagen deposition; and extracellular matrix remodeling. Inhibition of DDR2 decreased HSC-T6 cell proliferation and liver injury in rats with 10-week-induced alcoholic liver disease. DDR2 may have an important role in the pathogenesis of early-stage alcoholic liver disease. Silencing DDR2 may be effective in preventing early-stage alcoholic liver disease. Discoidin domain receptor 2 (DDR2) is involved in fibrotic disease. However, the exact pathogenic implications of the receptor in early alcoholic liver disease are still controversial. We constructed plasmid vectors encoding short-hairpin RNA against DDR2 to investigate its role in alcoholic liver disease in an immortalized rat hepatic stellate cell line, HSC-T6, and in rats by MTT, RT-PCR and western blot analyses; immunohistochemistry and electron microscopy. Alcohol-induced upregulation of DDR2 was associated with the expression of matrix metalloproteinase 2, the transforming growth factor [beta]1 signaling pathway and tissue inhibitor of metalloproteinase 1; collagen deposition; and extracellular matrix remodeling. Inhibition of DDR2 decreased HSC-T6 cell proliferation and liver injury in rats with 10-week-induced alcoholic liver disease. DDR2 may have an important role in the pathogenesis of early-stage alcoholic liver disease. Silencing DDR2 may be effective in preventing early-stage alcoholic liver disease. Discoidin domain receptor 2 (DDR2) is involved in fibrotic disease. However, the exact pathogenic implications of the receptor in early alcoholic liver disease are still controversial. We constructed plasmid vectors encoding short-hairpin RNA against DDR2 to investigate its role in alcoholic liver disease in an immortalized rat hepatic stellate cell line, HSC-T6, and in rats by MTT, RT-PCR and western blot analyses; immunohistochemistry and electron microscopy. Alcohol-induced upregulation of DDR2 was associated with the expression of matrix metalloproteinase 2, the transforming growth factor β1 signaling pathway and tissue inhibitor of metalloproteinase 1; collagen deposition; and extracellular matrix remodeling. Inhibition of DDR2 decreased HSC-T6 cell proliferation and liver injury in rats with 10-week-induced alcoholic liver disease. DDR2 may have an important role in the pathogenesis of early-stage alcoholic liver disease. Silencing DDR2 may be effective in preventing early-stage alcoholic liver disease.Discoidin domain receptor 2 (DDR2) is involved in fibrotic disease. However, the exact pathogenic implications of the receptor in early alcoholic liver disease are still controversial. We constructed plasmid vectors encoding short-hairpin RNA against DDR2 to investigate its role in alcoholic liver disease in an immortalized rat hepatic stellate cell line, HSC-T6, and in rats by MTT, RT-PCR and western blot analyses; immunohistochemistry and electron microscopy. Alcohol-induced upregulation of DDR2 was associated with the expression of matrix metalloproteinase 2, the transforming growth factor β1 signaling pathway and tissue inhibitor of metalloproteinase 1; collagen deposition; and extracellular matrix remodeling. Inhibition of DDR2 decreased HSC-T6 cell proliferation and liver injury in rats with 10-week-induced alcoholic liver disease. DDR2 may have an important role in the pathogenesis of early-stage alcoholic liver disease. Silencing DDR2 may be effective in preventing early-stage alcoholic liver disease. |
Audience | Academic |
Author | Liu, Huimin Ma, Xiangxing Sun, Xiaomeng Yan, Ming Guo, Rong Cui, Ruibing Luo, Zheng |
AuthorAffiliation | 1 Department of Geriatric Gastroenterology, Qilu Hospital of Shandong University, Jinan, Shandong, China 3 Department of Hepatology and Gastroenterology of Yantai Yuhuangding Hospital of Qingdao University Medical College, Yantai, Shandong, China 2 Key Laboratory of Cardiovascular Remodeling, Qilu Hospital of Shandong University, Jinan, Shandong, China 4 Department of Radiology, Qilu Hospital of Shandong University, Jinan, Shandong, China National Institutes of Health, United States of America |
AuthorAffiliation_xml | – name: 4 Department of Radiology, Qilu Hospital of Shandong University, Jinan, Shandong, China – name: 3 Department of Hepatology and Gastroenterology of Yantai Yuhuangding Hospital of Qingdao University Medical College, Yantai, Shandong, China – name: 1 Department of Geriatric Gastroenterology, Qilu Hospital of Shandong University, Jinan, Shandong, China – name: National Institutes of Health, United States of America – name: 2 Key Laboratory of Cardiovascular Remodeling, Qilu Hospital of Shandong University, Jinan, Shandong, China |
Author_xml | – sequence: 1 givenname: Zheng surname: Luo fullname: Luo, Zheng – sequence: 2 givenname: Huimin surname: Liu fullname: Liu, Huimin – sequence: 3 givenname: Xiaomeng surname: Sun fullname: Sun, Xiaomeng – sequence: 4 givenname: Rong surname: Guo fullname: Guo, Rong – sequence: 5 givenname: Ruibing surname: Cui fullname: Cui, Ruibing – sequence: 6 givenname: Xiangxing surname: Ma fullname: Ma, Xiangxing – sequence: 7 givenname: Ming surname: Yan fullname: Yan, Ming |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23409069$$D View this record in MEDLINE/PubMed |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Conceived and designed the experiments: ZL HML MY XXM. Performed the experiments: ZL HML XMS RG RBC. Analyzed the data: ZL. Contributed reagents/materials/analysis tools: ZL MY XXM. Wrote the paper: ZL. Competing Interests: The authors have declared that no competing interests exist. |
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Snippet | Discoidin domain receptor 2 (DDR2) is involved in fibrotic disease. However, the exact pathogenic implications of the receptor in early alcoholic liver disease... |
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SubjectTerms | Acetaldehyde - pharmacology Alcohol Alcohols Animals Apoptosis Apoptosis - genetics Biology Cell Line Cell Proliferation Collagen Collagen Type I - genetics Collagen Type I - metabolism Computer memory Diabetes Discoidin Domain Receptors Disease Models, Animal Electron microscopy Extracellular matrix Fibrosis Gangrene Gastroenterology Gene expression Gene Expression Regulation - drug effects Genetic vectors Geriatrics Growth factors Hepatic Stellate Cells - drug effects Hepatic Stellate Cells - metabolism Hepatitis Hepatocytes Hospitals Immunohistochemistry Kinases Liver Liver - metabolism Liver - pathology Liver cirrhosis Liver diseases Liver Diseases, Alcoholic - genetics Liver Diseases, Alcoholic - metabolism Liver Diseases, Alcoholic - pathology Male Matrix metalloproteinase Matrix Metalloproteinase 2 - metabolism Medicine Metalloproteinase Microscopy Necrosis - genetics Pathogenesis Polymerase chain reaction Rats Receptor Protein-Tyrosine Kinases - genetics Receptor Protein-Tyrosine Kinases - metabolism Receptors, Mitogen - genetics Receptors, Mitogen - metabolism Ribonucleic acid RNA RNA Interference RNA, Small Interfering - genetics RNA, Small Interfering - metabolism RNA-mediated interference Rodents Signal transduction Signal Transduction - drug effects Signaling Tissue inhibitor of metalloproteinase 1 Tissue Inhibitor of Metalloproteinase-1 - genetics Tissue Inhibitor of Metalloproteinase-1 - metabolism Transfection Transforming growth factor Transforming Growth Factor beta1 - metabolism |
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Title | RNA Interference against Discoidin Domain Receptor 2 Ameliorates Alcoholic Liver Disease in Rats |
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