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Lactacystin inhibits 3T3-L1 adipocyte differentiation through induction of CHOP-10 expression.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2006 Nov 10; Vol. 350 (1), pp. 1-6. Date of Electronic Publication: 2006 Sep 12. - Publication Year :
- 2006
-
Abstract
- Hormonal induction triggers a cascade leading to the expression of CCAAT/enhancer-binding protein(C/EBP)alpha and peroxisome proliferator-activated receptor (PPAR) gamma, C/EBPalpha, and PPARgamma turns on series of adipocyte genes that give rise to the adipocyte phenotype. Previous findings indicate that C/EBPbeta, a transcriptional activator of the C/EBPalpha and PPARgamma genes, is rapidly expressed after induction, but lacks DNA-binding activity and therefore cannot activate transcription of the C/EBPalpha and PPARgamma genes early in the differentiation program. Acquisition of DNA-binding activity of C/EBPbeta occurs when CHOP-10, a dominant-negative form of C/EBP family members, is down-regulated and becomes hyperphosphorylated as preadipocytes traverse the G1-S checkpoint of mitotic clonal expansion. Evidences are presented in this report that lactacystin, a proteasome inhibitor, up-regulated the CHOP-10 expression, blocked the DNA-binding activity of C/EBPbeta, and subsequently inhibited MCE as well as adipocyte differentiation.
- Subjects :
- 3T3-L1 Cells
Acetylcysteine pharmacology
Adipocytes cytology
Animals
CCAAT-Enhancer-Binding Protein-beta metabolism
Cyclin-Dependent Kinase 2 metabolism
DNA metabolism
Mice
Mitosis drug effects
Protein Binding
Transcription Factor CHOP genetics
Up-Regulation
Acetylcysteine analogs & derivatives
Adipocytes drug effects
Adipocytes metabolism
Cell Differentiation drug effects
Transcription Factor CHOP metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 350
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 16996026
- Full Text :
- https://doi.org/10.1016/j.bbrc.2006.08.188