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Inhibition of microRNA122 decreases SREBP1 expression by modulating suppressor of cytokine signaling 3 expression
- Source :
- Biochemical and Biophysical Research Communications. 438:230-235
- Publication Year :
- 2013
- Publisher :
- Elsevier BV, 2013.
-
Abstract
- While inhibition of microRNA122 (miR122) function in vivo results in reduced serum cholesterol and fatty acid levels, the molecular mechanisms underlying the link between miR122 function and lipid metabolism remains unclear. Because the expression of SREBP1, a central transcription factor involved in lipid metabolism, is known to be increased by suppressor of cytokine signaling 3 (SOCS3) expression, and because we previously found that SOCS3 expression is regulated by miR122, in this study, we examined the correlation between miR122 status and the expression levels of SOCS3 and SREBP1. SREBP1 expression decreased when SOCS3 expression was reduced by miR122 silencing in vitro. Conversely, SREBP1 expression in miR122-silenced cells was restored by enforced expression of SOCS3. Such correlations were observed in human liver tissues with different miR122 expression levels. These signaling links may explain one of the molecular mechanisms linking inhibition of miR122 function or decreased expression of miR122 to decreased fatty acid and cholesterol levels, in the inhibition of miR122 function, or in pathological status in chronic liver diseases.
- Subjects :
- Biophysics
Down-Regulation
Suppressor of Cytokine Signaling Proteins
Biology
Biochemistry
Cell Line
Suppression, Genetic
In vivo
Cell Line, Tumor
microRNA
Humans
Gene silencing
Gene Silencing
SOCS3
Molecular Biology
Transcription factor
chemistry.chemical_classification
digestive, oral, and skin physiology
Fatty acid
Lipid metabolism
Cell Biology
Sterol regulatory element-binding protein
Cell biology
MicroRNAs
Gene Expression Regulation
chemistry
Suppressor of Cytokine Signaling 3 Protein
Hepatocytes
Sterol Regulatory Element Binding Protein 1
Signal Transduction
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 438
- Database :
- OpenAIRE
- Journal :
- Biochemical and Biophysical Research Communications
- Accession number :
- edsair.doi.dedup.....498b14297ba177c0f86974ce123e514f
- Full Text :
- https://doi.org/10.1016/j.bbrc.2013.07.064