Inhibition of lipid droplet formation by Ser/Thr protein phosphatase PPM1D inhibitor, SL-176.
Rui KamadaNozomi KimuraFumihiko YoshimuraKeiji TaninoKazuyasu SakaguchiPublished in: PloS one (2019)
Obesity is a worldwide public health problem, which is associated with various severe diseases including diabetes, hypertension, atherosclerosis, and cancer. Recent studies have revealed that combination treatment of several different compounds using low doses is effective to reduce side effects. Thus, there is a need to develop an efficient inhibitor for reducing lipid droplets with a divergent target/pathway. Ser/Thr protein phosphatase PPM1D is involved in cellular metabolic processes and is a promising target for anti-obesity treatment. We have previously developed a potent and specific PPM1D inhibitor, SL-176. In this study, we demonstrated that significant reduction of lipid droplet formation in adipocytes by the PPM1D specific inhibitor, SL-176. Using Oil-red O staining and fluorescent imaging of lipid droplet, we found that treatment of SL-176 significantly suppressed lipid droplet formation of 3T3-L1 cells both in amount and in size. SL-176 also repressed mRNA and protein expression of PPARγ and C/EBPα, adipogenic markers, at nontoxic conditions. Thus, SL-176 is a unique and potent inhibitor of lipid droplet formation that acts via PPM1D, a novel target toward inhibiting adipocyte differentiation.
Keyphrases
- fatty acid
- single cell
- insulin resistance
- public health
- high throughput
- type diabetes
- adipose tissue
- metabolic syndrome
- cardiovascular disease
- blood pressure
- induced apoptosis
- weight loss
- squamous cell carcinoma
- oxidative stress
- binding protein
- high resolution
- physical activity
- body mass index
- young adults
- high fat diet induced
- flow cytometry
- cell death
- global health
- glycemic control
- smoking cessation
- childhood cancer