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 inPloS one Vol. 8; no. 2; p. e55860
Main Authors Luo, Zheng, Liu, Huimin, Sun, Xiaomeng, Guo, Rong, Cui, Ruibing, Ma, Xiangxing, Yan, Ming
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 07.02.2013
Public Library of Science (PLoS)
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RNA
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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.
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
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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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SSID ssj0053866
Score 2.199076
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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doaj
pubmedcentral
proquest
gale
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage e55860
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
URI https://www.ncbi.nlm.nih.gov/pubmed/23409069
https://www.proquest.com/docview/1330877554
https://www.proquest.com/docview/1288311420
https://pubmed.ncbi.nlm.nih.gov/PMC3567027
https://doaj.org/article/8420141b74e04256844f881a2d4c4080
http://dx.doi.org/10.1371/journal.pone.0055860
Volume 8
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