RMR-Related DNAJC6 Expression Suppresses Adipogenesis in 3T3-L1 Cells.
Juhee KimMyoungsook LeePublished in: Cells (2022)
Obesity causes various complications such as type 2 diabetes, hypertension, fatty liver, cardiovascular diseases, and cancer. In a pilot GWAS study, we screened the DNAJC6 gene which is significantly related to the resting metabolic rate (RMR) in childhood obesity. With DNAJC6 -overexpressed 3T3-L1 cells (Tg Hsp ), we investigated the new obesity mechanism caused by an energy imbalance. After differentiation, lipid droplets (Oil red O staining) were not formed in Tg Hsp cells compared to the control. Tg Hsp preadipocyte fibroblast morphology was also not clearly observed in the cell morphology assay (DAPI/BODIPY). In Tg Hsp cells, the expression of PPARγ, C/EBPα, and aP2 (adipogenesis-related biomarkers) decreased 3-, 39-, and 200-fold, respectively. The expression of the adipokines leptin and adiponectin from adipose tissues also decreased 2.4- and 840-fold, respectively. In addition, the levels of pHSL(Ser563) and free glycerol, which are involved in lipolysis, were significantly lower in Tg Hsp cells than in the control. The reduction in insulin receptor expression in Tg Hsp cells suppressed insulin signaling systems such as AKT phosphorylation, and GLUT4 expression. Degradation of IRS-1 in 3T3-L1 adipocytes was caused by chronic exposure to insulin, but not Tg Hsp . Mitochondrial functions such as oxygen consumption and ATP production, as well as proton leak and UCP1 protein expression, decreased in Tg Hsp cells compared to the control. Moreover, autophagy was observed by increasing autophagosomal proteins, LC3, on Day 8 of differentiation in Tg Hsp cells. Through our first report on the DNAJC6 gene related to RMR , we found a new mechanism related to energy metabolism in obesity. DNAJC6 expression positively suppressed adipogenesis, leading to the subsequent resistance of lipolysis, adipokine expression, insulin signaling, and mitochondrial functions.
Keyphrases
- type diabetes
- induced apoptosis
- heat shock protein
- cell cycle arrest
- poor prognosis
- signaling pathway
- endoplasmic reticulum stress
- heat stress
- insulin resistance
- metabolic syndrome
- oxidative stress
- adipose tissue
- cardiovascular disease
- blood pressure
- heat shock
- binding protein
- randomized controlled trial
- glycemic control
- cell proliferation
- risk factors
- genome wide
- gene expression
- cardiovascular risk factors
- high throughput
- skeletal muscle
- copy number
- high fat diet induced
- physical activity
- young adults
- high resolution
- body mass index
- transcription factor
- heart rate variability
- gas chromatography
- fluorescent probe
- atomic force microscopy