Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Mussbacher, M; Stessel, H; Pirker, T; Gorren, ACF; Mayer, B; Schrammel, A.
S-nitrosoglutathione inhibits adipogenesis in 3T3-L1 preadipocytes by S-nitrosation of CCAAT/enhancer-binding protein β.
Sci Rep. 2019; 9(1): 15403 Doi: 10.1038/s41598-019-51579-x [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Co-Autor*innen der Med Uni Graz
Pirker Teresa Marie
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
Murine 3T3-L1 adipocytes share many similarities with primary fat cells and represent a reliable in vitro model of adipogenesis. The aim of this study was to probe the effect of S-nitrosoglutathione (GSNO) on adipocyte differentiation. Adipogenesis was induced with a mixture of insulin, dexamethasone, and 3-isobutyl-1-methylxanthine in the absence and presence of increasing GSNO concentrations. Biochemical analysis after 7 days of differentiation showed a prominent anti-adipogenic effect of GSNO which was evident as reduced cellular triglycerides and total protein content as well as decreased mRNA and protein expression of late transcription factors (e.g. peroxisome proliferator activated receptor γ) and markers of terminal differentiation (e.g. leptin). By contrast, the nitrosothiol did not affect mRNA and protein expression of CCAAT/enhancer-binding protein β (C/EBPβ), which represents a pivotal early transcription factor of the adipogenic cascade. Differentiation was also inhibited by the NO donor (Z)-1-[2-(2-aminoethyl)-N-(2-ammonioethyl)amino]diazen-1-ium-1,2-diolate. Biotin switch experiments showed significantly increased S-nitrosation of C/EBPβ variants indicating that posttranslational S-nitrosative modification of this transcription factor accounts for the observed anti-adipogenic effect of NO. Our results suggest that S-nitrosation might represent an important physiological regulatory mechanism of fat cell maturation.
Find related publications in this database (using NLM MeSH Indexing)
1-Methyl-3-isobutylxanthine - pharmacology
3T3-L1 Cells - administration & dosage
Adipocytes - cytology, drug effects, metabolism
Adipogenesis - administration & dosage
Animals - administration & dosage
CCAAT-Enhancer-Binding Protein-beta - genetics, metabolism
Dexamethasone - pharmacology
Insulin - pharmacology
Leptin - genetics, metabolism
Mice - administration & dosage
Nitric Oxide Donors - pharmacology
PPAR gamma - genetics, metabolism
S-Nitrosoglutathione - pharmacology

© Med Uni Graz Impressum