Objective:Myeloma bone disease(MBD)is the most common complication of multiple myeloma(MM).Our previous study showed that the serum levels of C3/C4 in MM patients were significantly positively correlated with the seve...Objective:Myeloma bone disease(MBD)is the most common complication of multiple myeloma(MM).Our previous study showed that the serum levels of C3/C4 in MM patients were significantly positively correlated with the severity of bone disease.However,the mechanism of C3 a/C4 a in osteoclasts MM patients remains unclear.Methods:The formation and function of osteoclasts were analyzed after adding C3 a/C4 a in vitro.RNA-seq analysis was used to screen the potential pathways affecting osteoclasts,and the results were verified by Western blot,q RT-PCR,and pathway inhibitors.Results:The osteoclast area per view induced by 1μg/m L(mean±SD:50.828±12.984%)and 10μg/m L(53.663±12.685%)of C3 a was significantly increased compared to the control group(0μg/m L)(34.635±8.916%)(P<0.001 and P<0.001,respectively).The relative m RNA expressions of genes,OSCAR/TRAP/RANKL/cathepsin K,induced by 1μg/m L(median:5.041,3.726,1.638,and 4.752,respectively)and 10μg/m L(median:5.140,3.702,2.250,and 5.172,respectively)of C3 a was significantly increased compared to the control group(median:3.137,2.004,0.573,and 2.257,respectively)(1μg/m L P=0.001,P=0.003,P<0.001,and P=0.008,respectively;10μg/m L:P<0.001,P=0.019,P<0.001,and P=0.002,respectively).The absorption areas of the osteoclast resorption pits per view induced by 1μg/m L(mean±SD:51.464±11.983%)and 10μg/m L(50.219±12.067%)of C3 a was also significantly increased(33.845±8.331%)(P<0.001 and P<0.001,respectively)compared to the control.There was no difference between the C4 a and control groups.RNA-seq analysis showed that C3 a promoted the proliferation of osteoclasts using the phosphoinositide 3-kinase(PI3 K)signaling pathway.The relative expressions of PIK3 CA/phosphoinositide dependent kinase-1(PDK1)/serum and glucocorticoid inducible protein kinases(SGK3)genes and PI3 K/PDK1/p-SGK3 protein in the C3 a group were significantly higher than in the control group.The activation role of C3 a in osteoclasts of MM patients was reduced by the SGK inhibitor(EMD638683).Conclusions:C3 a activated osteoclasts by regulating the PI3 K/PDK1/SGK3 pathways in MM patients,which was reduced using a SGK inhibitor.Overall,our results identified potential therapeutic targets and strategies for MBD patients。展开更多
目的通过孕兔羊水栓塞动物模型测定凝血功能、补体C3a的含量以及补体C3a在肺组织中的表达,初步探索羊水栓塞(AFE)的发病机制。方法健康妊娠晚期孕兔随机分3组(对照组、羊水组、羊水胎粪组),暴露子宫抽取羊水、胎粪。按2.5 m L/Kg注入自...目的通过孕兔羊水栓塞动物模型测定凝血功能、补体C3a的含量以及补体C3a在肺组织中的表达,初步探索羊水栓塞(AFE)的发病机制。方法健康妊娠晚期孕兔随机分3组(对照组、羊水组、羊水胎粪组),暴露子宫抽取羊水、胎粪。按2.5 m L/Kg注入自体羊水、羊水胎粪混合液(羊水原液与胎粪按质量比配成1%混合液)入血,对照组注入等剂量生理盐水。注射30 min后取血分别用血凝仪测凝血功能(凝血酶原时间(PT)、活化部分凝血活酶时间(APTT)、凝血酶时间(TT)、纤维蛋白原(FIB))及ELISA法测血浆补体C3a含量。取血后10%KCl处死孕兔,取孕兔双肺做病理学检查。结果1补体C3a浓度:羊水组、羊水胎粪组补体C3a含量降低(P<0.05);2凝血功能检查结果:PT、APTT、TT羊水组、羊水胎粪组延长(P<0.05),FIB羊水组、羊水胎粪组降低(P<0.05)。结论 1发生AFE时补体C3a含量降低,说明补体系统被激活,消耗补体成分发生类过敏反应;2AFE时PT、TT、APTT均延长,FIB降低,说明AFE时有发展为DIC的趋势。展开更多
基金supported by the National Natural Science Foundation of China(Grant Nos.81770110,81900131,and 82000219)the Anticancer Major Special Project of Tianjin(Grant No.12ZCDZSY18000)+4 种基金the Tianjin Municipal Natural Science Foundation(Grant Nos.18JCYBJC27200 and 18JCQNJC80400)the Tianjin Education Commission Research Project(Grant Nos.2018KJ043 and 2018KJ045)the Tianjin Health and Family Planning Commission(Grant No.15KG150)the Youth Incubation Fund of Tianjin Medical University General Hospital(Grant No.ZYYFY2019020)the Tianjin Science and Technology Planning Project(Grant No.20YFZCSY00060)。
文摘Objective:Myeloma bone disease(MBD)is the most common complication of multiple myeloma(MM).Our previous study showed that the serum levels of C3/C4 in MM patients were significantly positively correlated with the severity of bone disease.However,the mechanism of C3 a/C4 a in osteoclasts MM patients remains unclear.Methods:The formation and function of osteoclasts were analyzed after adding C3 a/C4 a in vitro.RNA-seq analysis was used to screen the potential pathways affecting osteoclasts,and the results were verified by Western blot,q RT-PCR,and pathway inhibitors.Results:The osteoclast area per view induced by 1μg/m L(mean±SD:50.828±12.984%)and 10μg/m L(53.663±12.685%)of C3 a was significantly increased compared to the control group(0μg/m L)(34.635±8.916%)(P<0.001 and P<0.001,respectively).The relative m RNA expressions of genes,OSCAR/TRAP/RANKL/cathepsin K,induced by 1μg/m L(median:5.041,3.726,1.638,and 4.752,respectively)and 10μg/m L(median:5.140,3.702,2.250,and 5.172,respectively)of C3 a was significantly increased compared to the control group(median:3.137,2.004,0.573,and 2.257,respectively)(1μg/m L P=0.001,P=0.003,P<0.001,and P=0.008,respectively;10μg/m L:P<0.001,P=0.019,P<0.001,and P=0.002,respectively).The absorption areas of the osteoclast resorption pits per view induced by 1μg/m L(mean±SD:51.464±11.983%)and 10μg/m L(50.219±12.067%)of C3 a was also significantly increased(33.845±8.331%)(P<0.001 and P<0.001,respectively)compared to the control.There was no difference between the C4 a and control groups.RNA-seq analysis showed that C3 a promoted the proliferation of osteoclasts using the phosphoinositide 3-kinase(PI3 K)signaling pathway.The relative expressions of PIK3 CA/phosphoinositide dependent kinase-1(PDK1)/serum and glucocorticoid inducible protein kinases(SGK3)genes and PI3 K/PDK1/p-SGK3 protein in the C3 a group were significantly higher than in the control group.The activation role of C3 a in osteoclasts of MM patients was reduced by the SGK inhibitor(EMD638683).Conclusions:C3 a activated osteoclasts by regulating the PI3 K/PDK1/SGK3 pathways in MM patients,which was reduced using a SGK inhibitor.Overall,our results identified potential therapeutic targets and strategies for MBD patients。
文摘目的通过孕兔羊水栓塞动物模型测定凝血功能、补体C3a的含量以及补体C3a在肺组织中的表达,初步探索羊水栓塞(AFE)的发病机制。方法健康妊娠晚期孕兔随机分3组(对照组、羊水组、羊水胎粪组),暴露子宫抽取羊水、胎粪。按2.5 m L/Kg注入自体羊水、羊水胎粪混合液(羊水原液与胎粪按质量比配成1%混合液)入血,对照组注入等剂量生理盐水。注射30 min后取血分别用血凝仪测凝血功能(凝血酶原时间(PT)、活化部分凝血活酶时间(APTT)、凝血酶时间(TT)、纤维蛋白原(FIB))及ELISA法测血浆补体C3a含量。取血后10%KCl处死孕兔,取孕兔双肺做病理学检查。结果1补体C3a浓度:羊水组、羊水胎粪组补体C3a含量降低(P<0.05);2凝血功能检查结果:PT、APTT、TT羊水组、羊水胎粪组延长(P<0.05),FIB羊水组、羊水胎粪组降低(P<0.05)。结论 1发生AFE时补体C3a含量降低,说明补体系统被激活,消耗补体成分发生类过敏反应;2AFE时PT、TT、APTT均延长,FIB降低,说明AFE时有发展为DIC的趋势。
