Background: Pharmacological factors used to induce insulin resistance (IR) inin vitro models may not mimic the fullin vivo features of type 2 diabetes mellitus (T2DM). This study aimed to examine the ability of diabet...Background: Pharmacological factors used to induce insulin resistance (IR) inin vitro models may not mimic the fullin vivo features of type 2 diabetes mellitus (T2DM). This study aimed to examine the ability of diabetic serum (DS) to induce IR and investigate whether adipose-derived mesenchymal stem cell conditioned medium (ADMSC-CM) reverses DS-induced IR.Methods: DS was obtained from newly diagnosed T2DM patients. IR was induced in differentiated 3T3-L1 cells by employing dexamethasone, tumor necrosis factor alpha (TNF-α), palmitate and DS. Glucose uptake (2-[N-[7-nitrobenz-2-oxa-1,3-diazol-4-yl] amino]-2-deoxyglucose(2-NBDG) uptake assay), intracellular levels of reactive oxygen species (ROS), and superoxide radicals (O2-) (fluorescence microscopy and fluorometry) were analyzed in control and experimental samples. mRNA expression of key genes involved in glucose transport and inflammation were analyzed by using reverse transcription polymerase chain reaction (RT-PCR). Pro-inflammatory cytokines and phospho-insulin receptor substrate (IRS) (Ser-307) protein expression were analyzed by fluorescence activated cell sorter analysis. Statistical significance was determined by using one-way ANOVA followed by Tukey’s multiple comparison tests.Results: ADMSC-CM significantly increased the DS-mediated decrease in 2-NBDG uptake (11.01 ± 0.50vs. 7.20 ± 0.30,P < 0.01) and reduced DS-driven ROS (fluorescence count, 6.35 ± 0.46vs. 9.80 ± 0.10,P < 0.01) and O2- (fluorescence count, 3.00 ± 0.10vs. 4.60 ± 0.09,P < 0.01) production. Further, the ADMSC-CM restored DS-induced down regulation GLUT4 (1.52- fold,P < 0.05) as well as the up-regulation of PPARγ (0.35-fold,P < 0.01), and IKKβ (0.37-fold,P < 0.01) mRNA, and phospho-IRS (Ser-307) protein expression compared to the baseline (median fluorescence intensity, 88,192 ± 2720vs. 65,450 ± 3111,P < 0.01). DS induced IR, similar to the traditionally used pharmacological factors, namely dexamethasone, TNF-α, and palmitate, which can be attributed to the significantly higher pro-inflammatory cytokines levels (TNF-α (2.28 ± 0.03 pg/mLvs. 2.38 ± 0.03 pg/mL,P < 0.01), interleukin 6 (IL)-6 (1.94 ± 0.02 pg/mLvs. 2.17 ± 0.04 pg/mL,P < 0.01), IL-17 (2.16 ± 0.02 pg/mLvs. 2.22 ± 0.002 pg/mL,P < 0.05), and interferon gamma (IFN-γ) (2.07 ± 0.02 pg/mLvs. 2.15 ± 0.04 pg/mL,P < 0.05)) in DS.Conclusions: DS can be explored as a novel inducer of IR inin vitro studies with further standardization, substituting the conventionally used pharmacological factors. Our findings also affirm the validity of ADMSC-CM as a prospective insulin sensitizer for T2DM therapy.展开更多
文摘Background: Pharmacological factors used to induce insulin resistance (IR) inin vitro models may not mimic the fullin vivo features of type 2 diabetes mellitus (T2DM). This study aimed to examine the ability of diabetic serum (DS) to induce IR and investigate whether adipose-derived mesenchymal stem cell conditioned medium (ADMSC-CM) reverses DS-induced IR.Methods: DS was obtained from newly diagnosed T2DM patients. IR was induced in differentiated 3T3-L1 cells by employing dexamethasone, tumor necrosis factor alpha (TNF-α), palmitate and DS. Glucose uptake (2-[N-[7-nitrobenz-2-oxa-1,3-diazol-4-yl] amino]-2-deoxyglucose(2-NBDG) uptake assay), intracellular levels of reactive oxygen species (ROS), and superoxide radicals (O2-) (fluorescence microscopy and fluorometry) were analyzed in control and experimental samples. mRNA expression of key genes involved in glucose transport and inflammation were analyzed by using reverse transcription polymerase chain reaction (RT-PCR). Pro-inflammatory cytokines and phospho-insulin receptor substrate (IRS) (Ser-307) protein expression were analyzed by fluorescence activated cell sorter analysis. Statistical significance was determined by using one-way ANOVA followed by Tukey’s multiple comparison tests.Results: ADMSC-CM significantly increased the DS-mediated decrease in 2-NBDG uptake (11.01 ± 0.50vs. 7.20 ± 0.30,P < 0.01) and reduced DS-driven ROS (fluorescence count, 6.35 ± 0.46vs. 9.80 ± 0.10,P < 0.01) and O2- (fluorescence count, 3.00 ± 0.10vs. 4.60 ± 0.09,P < 0.01) production. Further, the ADMSC-CM restored DS-induced down regulation GLUT4 (1.52- fold,P < 0.05) as well as the up-regulation of PPARγ (0.35-fold,P < 0.01), and IKKβ (0.37-fold,P < 0.01) mRNA, and phospho-IRS (Ser-307) protein expression compared to the baseline (median fluorescence intensity, 88,192 ± 2720vs. 65,450 ± 3111,P < 0.01). DS induced IR, similar to the traditionally used pharmacological factors, namely dexamethasone, TNF-α, and palmitate, which can be attributed to the significantly higher pro-inflammatory cytokines levels (TNF-α (2.28 ± 0.03 pg/mLvs. 2.38 ± 0.03 pg/mL,P < 0.01), interleukin 6 (IL)-6 (1.94 ± 0.02 pg/mLvs. 2.17 ± 0.04 pg/mL,P < 0.01), IL-17 (2.16 ± 0.02 pg/mLvs. 2.22 ± 0.002 pg/mL,P < 0.05), and interferon gamma (IFN-γ) (2.07 ± 0.02 pg/mLvs. 2.15 ± 0.04 pg/mL,P < 0.05)) in DS.Conclusions: DS can be explored as a novel inducer of IR inin vitro studies with further standardization, substituting the conventionally used pharmacological factors. Our findings also affirm the validity of ADMSC-CM as a prospective insulin sensitizer for T2DM therapy.
