Effects of small GTP-binding protein GDP dissociation stimulator on adipocyte hypertrophy and glucose metabolism disorder in mice / 中华内科杂志

ABSTRACT

Objective: To explore the effect and mechanism of small GTP-binding protein GDP dissociation stimulator (SmgGDS) on the development of obesity. Methods: (1) 8-week-old C57BL/6J mice were randomly assigned to normal diet and high fat diet group, with 6 mice in each group. They were fed regular feed and a high fat diet containing 60% fat for 4 months, respectively. The expression of SmgGDS in epididymal adipose tissue (eWAT), liver, and skeletal muscle were measured using Western-blot. (2) 6-week-old wild-type (WT) and SmgGDS knockdown (KD) mice were divided into four groups, each receiving high fat diet for 4 months (7 in each group) and 7 months (9 in each group). Glucose tolerance test (GTT) and insulin tolerance test (ITT) were conducted; The weight, adipose tissue, and liver weight of mice were recorded; HE staining examined adipose tissue structural changes; Western-blot determined extracellular signal-regulated kinase (ERK) 1/2 phosphorylation levels in eWAT; Real time fluorescence quantitative polymerase chain reaction (RT-qPCR) was used to detect mRNA levels of CCAAT/enhancer binding protein α (C/EBPα), C/EBPβ and peroxisome proliferator activated receptor γ (PPARγ) in eWAT. (3) Mouse embryonic fibroblasts (MEFs) extracted from WT and KD mice were induced for differentiation. Oil red O staining and Western-blot were used to detect lipid droplet and expression of SmgGDS and phospho-ERK; C/EBPα, C/EBPβ and PPARγ mRNA levels were measured using RT-qPCR. (4) 10-week-old C57BL/6J mice were randomly assigned into two groups, with 7 mice in each group. Mice were infected with SmgGDS overexpressing adeno-associated virus (AAV-SmgGDS) or empty vector intraperitoneally, then fed with high fat diet. After 4 weeks, performed GTT and ITT; Recorded the weight and adipose tissue weight of mice; HE staining was used to analyze structural changes of eWAT; Western-blot was used to detect the phosphorylation level of ERK in eWAT. Results: (1) The expression of SmgGDS was significantly upregulated in eWAT of high fat diet fed mice (normal diet group 0.218±0.037, high fat diet group0.439±0.072, t=2.74, P=0.034). (2) At 4 months of high fat diet intervention, the glucose tolerance (60 minutes after glucose injection, WT group 528 mg/dl±21 mg/dl, KD group 435 mg/dl±17 mg/dl, t=3.47, P=0.030; 90 minutes, WT group 463 mg/dl±24 mg/dl, KD group 366 mg/dl±18 mg/dl, t=3.23, P=0.047;120 minutes, WT group 416 mg/dl±21 mg/dl, KD group 297 mg/dl±16 mg/dl, t=4.49, P=0.005) and insulin sensitivity (15 minutes after insulin injection, WT group 77.79%±3.45%, KD group 54.30%±2.92%, t=3.49, P=0.005; 30 minutes, WT group 62.27%±5.31%, KD group 42.25%±1.85%, t=2.978, P=0.024; 90 minutes, WT group 85.69%±6.63%, KD group 64.71%±5.41%, t=3.120, P=0.016) of KD mice were significantly improved compared to the WT group, with an increase in eWAT weight ratio (WT 4.19%±0.18%, KD 5.12%±0.37%, t=2.28, P=0.042), but a decrease in average adipocyte area (WT group 5221 μm²±241 μm², KD group 4410 μm²±196 μm², t=2.61, P=0.026). After 7 months of high fat diet, the eWAT weight ratio of KD mice decreased (WT 5.02%±0.20%, KD 3.88%±0.21%, t=3.92, P=0.001) and adipocyte size decreased (WT group 6 783 μm²±390 μm², KD group 4785 μm²±303 μm², t=4.05, P=0.002). The phospho-ERK1 in eWAT increased (WT group 0.174±0.056, KD group 0.588±0.147, t=2.64, P=0.025), and mRNA level of PPARγ significantly decreased (WT group 1.018±0.128, KD group 0.029±0.015, t=7.70, P=0.015). (3) The expression of SmgGDS was significantly increased in differentiated MEF (undifferentiated 6.789±0.511, differentiated 10.170±0.523, t=4.63, P=0.010); SmgGDS knock-down inhibited lipid droplet formation in MEF (WT group 1.00±0.02, KD group 0.88±0.02, t=5.05, P=0.007) and increased ERK1 (WT group 0.600±0.179, KD group 1.325±0.102, t=3.52, P=0.025) and ERK2 (WT group 2.179±0.687, KD group 5.200±0.814, t=2.84, P=0.047) activity, which can be reversed by ERK1/2 inhibitor. (4) SmgGDS over expression resulted in weight gain, increased eWAT weight (control group 3.29%±0.36%, AAV-SmgGDS group 4.27%±0.26%, t=2.20, P=0.048) and adipocyte size (control group 3525 μm²±454 μm², AAV-SmgGDS group 5326 μm²±655 μm², t=2.26, P=0.047), impaired insulin sensitivity(30 minutes after insulin injection, control group 44.03%±4.29%, AAV-SmgGDS group 62.70%±2.81%, t=3.06, P=0.019), and decreased ERK1 (control group 0.829±0.077, AAV-SmgGDS group 0.326±0.036, t=5.96, P=0.001)and ERK2 (control group 5.748±0.287, AAV-SmgGDS group 2.999±0.845, t=3.08, P=0.022) activity in eWAT. Conclusion: SmgGDS knockdown improves obesity related glucose metabolism disorder by inhibiting adipogenesis and adipose tissue hypertrophy, which is associated with ERK activation.