Objective:To study the effects and possible underlying mechanism of Qufeng Tongluo Prescription(祛风通络方,QFTL)on the regulation of mesangial cells(MCs)proliferation and apoptosis.Methods:The MCs used in this experim...Objective:To study the effects and possible underlying mechanism of Qufeng Tongluo Prescription(祛风通络方,QFTL)on the regulation of mesangial cells(MCs)proliferation and apoptosis.Methods:The MCs used in this experiment have undergone five passages induced by lipopolysaccharide(LPS).Changes in the proliferation,apoptosis,cell cycle regulatory proteins and mRNA expression levels of the MCs after administration of Benazepril or QFTL were measured by methyl thiazolyl tetrazolium(MTT)reduction assay,flow cytometry,Western blot and quantitative real-time polymerase chain reaction(qRT-PCR),respectively.Results:The addition of Benazepril or QFTL serum inhibited LPS-induced MC proliferation after treatment for 24,48 and72 h,respectively(P<0.05 or P<0.01).Moreover,the inhibitory effect is more significant in the QFTL group at48 h(P<0.05).Compared with the control group,LPS-induced cell proliferation decreased the number of cells in G1 phase versus cells in S and G2/M phases,while the addition of QFTL and Benazepril serum increased the ratio of cells at G1 phase(P<0.05 or P<0.01)to cells at S phase(P<0.01),implicating the cell cycle inhibition effect exerted by QFTL.LPS decreased the level of MC apoptosis,compared with the control group(P<0.05),while QFTL and Benazepril serum increased the level of MC apoptosis(P<0.01).Moreover,the difference between the QFTI_group and the Benazepril group was statistically significant(P<0.01).Compared with the control group,the protein and mRNA expression levels of cylinD1,cyclin dependent kinase 2(CDK2)and p21were significantly increased(P<0.05 or P<0.01),p27 was decreased but with no statistical significance(P>0.05);After being treated with QFTL and Benazepdl serum,the protein and mRNA expression levels of cylinD1,CDK2,p21 were decreased and p27 increased significantly(P<0.05 or P<0.01);Compared with the Benazepril group,QFTL show better effects on protein and mRNA expression levels of cylinD1,CDK2(P<0.05 or P<0.01)and p21protein expression(P<0.05).Conclusion:QFTL inhibits MCs proliferation,promotes MCs apoptosis through an underlying mechanism of down-regulating the protein and mRNA expression levels of cylinD1,CDK2,p21 and up-regulation of the expression level of p27.展开更多
基金Supported by the National Natural Science Foundation of China(No.30801504,No.30901926,No.81100530 and No.81070590)
文摘Objective:To study the effects and possible underlying mechanism of Qufeng Tongluo Prescription(祛风通络方,QFTL)on the regulation of mesangial cells(MCs)proliferation and apoptosis.Methods:The MCs used in this experiment have undergone five passages induced by lipopolysaccharide(LPS).Changes in the proliferation,apoptosis,cell cycle regulatory proteins and mRNA expression levels of the MCs after administration of Benazepril or QFTL were measured by methyl thiazolyl tetrazolium(MTT)reduction assay,flow cytometry,Western blot and quantitative real-time polymerase chain reaction(qRT-PCR),respectively.Results:The addition of Benazepril or QFTL serum inhibited LPS-induced MC proliferation after treatment for 24,48 and72 h,respectively(P<0.05 or P<0.01).Moreover,the inhibitory effect is more significant in the QFTL group at48 h(P<0.05).Compared with the control group,LPS-induced cell proliferation decreased the number of cells in G1 phase versus cells in S and G2/M phases,while the addition of QFTL and Benazepril serum increased the ratio of cells at G1 phase(P<0.05 or P<0.01)to cells at S phase(P<0.01),implicating the cell cycle inhibition effect exerted by QFTL.LPS decreased the level of MC apoptosis,compared with the control group(P<0.05),while QFTL and Benazepril serum increased the level of MC apoptosis(P<0.01).Moreover,the difference between the QFTI_group and the Benazepril group was statistically significant(P<0.01).Compared with the control group,the protein and mRNA expression levels of cylinD1,cyclin dependent kinase 2(CDK2)and p21were significantly increased(P<0.05 or P<0.01),p27 was decreased but with no statistical significance(P>0.05);After being treated with QFTL and Benazepdl serum,the protein and mRNA expression levels of cylinD1,CDK2,p21 were decreased and p27 increased significantly(P<0.05 or P<0.01);Compared with the Benazepril group,QFTL show better effects on protein and mRNA expression levels of cylinD1,CDK2(P<0.05 or P<0.01)and p21protein expression(P<0.05).Conclusion:QFTL inhibits MCs proliferation,promotes MCs apoptosis through an underlying mechanism of down-regulating the protein and mRNA expression levels of cylinD1,CDK2,p21 and up-regulation of the expression level of p27.
