[Objective]Cells are sensitive to oxidative stress and elevated levels of intracellular reactive oxygen species during in vitro culture,which affects cell function.In this research,the regulation of reactive oxygen species in porcine adipose mesenchymal stem cells by N-acetyl-L cysteine(NAC)was evaluated,and the effects on their proliferation and differentiation were further clarified,which could provide a theoretical basis and reference for cultured fat seed cells to expand in vitro in large numbers and improve differentiation efficiency.[Method]In this research,to model oxidative stress,the different concentrations of H2O2(0,25,50,and 100 μmol·L-1)were added during the proliferation of adipose-derived mesenchymal stem cells(ADSCs).The added concentration of H2O2 was identified by cell counting results,cell morphology,cell viability and intracellular reactive oxygen species levels detected by a High-throughput High-content Live Cells Confocal Imaging System.To select the appropriate addition concentration of NAC to promote the proliferation of ADSCs,the different concentrations of NAC(0,1,2,and 3 mmol·L-1)were added during the proliferation of ADSCs,and the appropriate addition concentration of NAC was determined by cell counting results and cell morphology.To further explore the effect of NAC on the proliferation of oxidatively stressed ADSCs,cell proliferation under different treatment conditions(Control,1 mmol·L-1 NAC,50 μmol·L-1 H2O2,and 1 mmol·L-1 NAC + 50 μmol·L-1 H2O2)was analyzed by EdU staining and cell counting.To investigate the level of reactive oxygen species in ADSCs under different treatment conditions,ADSCs proliferated under different treatment conditions for 3 d were stained by CellRox,and the intracellular reactive oxygen species content was detected by High-throughput High-inclusion Live Cell Confocal Imaging System to clarify the relationship between ADSCs proliferation and intracellular reactive oxygen species level.To explore the effect of reactive oxygen species levels within ADSCs on their differentiation,ADSCs were stained with Oil Red O after 10 d of differentiation under different treatment conditions,and the amount of differentiated lipid accumulation in ADSCs was assessed by Image J analysis of stained area,and the relative expression of ADSCs differentiation-related genes was examined by RT-qPCR.[Result]During the proliferation of ADSCs,ADSCs in the group with 50 μmol·L-1 H2O2 were shuttle-shaped and had significantly higher intracellular reactive oxygen species content compared with the control group(P＜0.05),and the oxidative stress model was successfully established.Compared with the control group,when 50 μmol·L-1 H2O2 was added during proliferation of ADSCs,the number of ADSCs proliferation was significantly decreased(P＜0.05),but the lipid accumulation of ADSCs was significantly higher(P＜0.05)when 50 μmol·L-1 H2O2 was added during the differentiation of ADSCs.During the proliferation of ADSCs,ADSCs in the group with the addition of 1 mmol·L-1 NAC had a shuttle shape,the intracellular reactive oxygen species content was significantly lower(P＜0.05),and proliferation number of ADSCs was significantly higher(P＜0.05)compared with the control group,but the addition of 1 mmol·L-1 NAC during the differentiation of ADSCs had no significant effect on the lipid accumulation of ADSCs(P＞0.05).[Conclusion]When ADSCs were affected by oxidative stress,the level of reactive oxygen species in ADSCs increases,which was detrimental to the massive expansion of ADSCs in vitro,inducing cell differentiation and accelerating cellular senescence.The addition of 1 mmol·L-1 NAC to the in vitro expansion system of ADSCs could reduce the oxidative stress damage brought about by long-term culture and exogenous stimulation,and had a protective effect on oxidatively stressed ADSCs,which could effectively promote cell proliferation and did not affect the differentiation ability of the cells.
国家科技期刊平台
NSTL
万方数据
维普
