Retinoic acid modulates lipid accumulation glucose concentration dependently through inverse regulation of SREBP-1 expression in 3T3L1 adipocytes.
Mabrouk Attia Abd EldaimShinya MatsuokaYuko Okamatsu-OguraAkihiro KamikawaMohamed Mohamed AhmedAkira TeraoKei-Ichi NakajimaKazuhiro KimuraPublished in: Genes to cells : devoted to molecular & cellular mechanisms (2017)
It is well known that retinoic acid (RA) suppresses adipogenesis, although there are some contradicting reports. In this study, we examined the effect of extracellular glucose on RA-induced suppression of adipogenesis in 3T3L1 cell culture. When the cells were cultured in normal glucose medium (NG), the addition of RA suppressed lipid accumulation. However, when cultured in high glucose medium (HG), addition of RA to the cells enhanced lipid accumulation. These changes were accompanied by parallel alterations in fatty acid synthase (FAS) and sterol regulatory element-binding protein (SREBP)-1 gene expression. Transfection of SREBP-1 siRNA suppressed RA-induced enhancement of lipid accumulation and FAS expression in the cells cultured with HG. Transfection of the nuclear form of SREBP-1a cDNA into the cells cultured with NG inhibited RA-induced suppression of lipid accumulation and FAS expression. Moreover, RA- and HG-induced SREBP-1a expression occurred at the early phase of adipogenesis and was dependent on glucocorticoid to induce liver X receptor (LXR) β, peroxisomal proliferator-activated receptor (PPAR) γ and retinoid X receptor (RXR), the key nuclear factors influencing the SREBP-1a gene expression. These results suggest that RA suppresses and enhances lipid accumulation through extracellular glucose concentration-dependent modulation of SREBP-1 expression.
Keyphrases
- high glucose
- endothelial cells
- binding protein
- rheumatoid arthritis
- induced apoptosis
- poor prognosis
- gene expression
- disease activity
- diabetic rats
- signaling pathway
- fatty acid
- ankylosing spondylitis
- blood glucose
- systemic lupus erythematosus
- dna methylation
- oxidative stress
- endoplasmic reticulum stress
- skeletal muscle
- systemic sclerosis
- electronic health record
- living cells
- single molecule
- drug delivery
- aqueous solution