首页|BMP7过表达慢病毒载体构建及其对小鼠主动脉平滑肌细胞钙化的影响

BMP7过表达慢病毒载体构建及其对小鼠主动脉平滑肌细胞钙化的影响

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目的 构建骨形态发生蛋白7(BMP7)过表达慢病毒载体,分析BMP7过表达对小鼠主动脉内皮细胞Jagged1表达的影响及其对共培养血管平滑肌细胞(VSMCs)钙化的影响.方法 根据目的基因信息Mouse-BMP7(NM_007557.3)和质粒信息pLVX-zsGreen-C1进行基因序列合成,构建BMP7过表达慢病毒.qPCR检测BMP7过表达慢病毒感染效率;Western blot检测其感染的小鼠主动脉内皮细胞Jagged1蛋白表达.将过表达BMP7慢病毒感染的内皮细胞与VSMCs共培养,茜素红染色观察共培养后VSMCs钙化情况.结果 成功构建BMP7过表达慢病毒载体并转染至小鼠主动脉内皮细胞.qPCR检测结果提示,与正常对照组比较,BMP7过表达组的BMP7 mRNA相对表达量显著升高(P<0.01),空载体对照组BMP7 mRNA无显著变化(P>0.05).Western blot结果显示,BMP7过表达组内皮细胞Jagged1蛋白表达水平较正常对照组显著降低(P<0.01),而空载体对照组内皮细胞Jagged1蛋白水平较正常对照组无显著改变(P>0.05).茜素红染色结果提示,与感染过表达BMP7慢病毒的内皮细胞共培养后,VSMCs的钙化程度明显增加.结论 成功构建小鼠BMP7过表达慢病毒载体,并发现过表达BMP7可以降低小鼠主动脉内皮细胞Jagged1表达,并促进共培养的VSMCs钙化.
BMP7 overexpression lentiviral vector construction and its effect on calcification of mouse aortic smooth muscle cells
Objective To construct a lentiviral vector for overexpression of bone morphogenetic protein 7(BMP7)in mice,and the effect of BMP7 overexpression on the expression of Jagged1 in mouse aortic endothelial cells and the calcification of the co-cultured vascular smooth muscle cells(VSMCs)were analyzed.Methods According to the target gene information Mouse-BMP7(NM_007557.3)and plasmid information pLVX-zsGreen-C1,gene sequence synthesis was carried out to construct BMP7 overexpression lentivirus.The efficiency of BMP7 overexpression lentivirus infection was detected by qPCR;the expression of Jagged1 protein in aortic endothelial cells from infected mice was detected by Western blot.The endothelial cells with lentivirus overexpressing BMP7 were co-cultured with VSMCs,and the calcification of VSMCs was observed by alizarin red staining.Results BMP7 overexpression lentiviral vector was successfully constructed and transfected into aortic endothelial cells.qPCR test results showed that the expression level of BMP7 mRNA was significantly increased in the BMP7 overexpression group than that in the normal control group(P<0.01),while there was no significant difference in the expression of BMP7 mRNA between the empty vector control group and the normal control group(P>0.05).Western blot results showed that the expression level of Jagged1 protein in endothelial cells of mouse in the BMP7 overexpression group was significantly lower than that in the normal control group(P<0.01),while there was no significant difference in the expression level of Jagged1 protein in endothelial cells between the empty vector control group and the normal control group(P>0.05).The results of alizarin red staining showed that the calcification of VSMCs was significantly increased after co-cultured with endothelial cells infected with BMP7 lentivirus.Conclusion Mouse BMP7 overexpression lentiviral vector was successfully constructed,and overexpression of BMP7 can reduce the expression of Jagged1 in mouse aortic endothelial cells and promote the calcification of co-cultured VSMCs.

bone morphological protein 7lentiviral vector constructionJagged1vascular calcification

付仕林、易雪娇、潘文旭、尹纯、康华利、钱德慧

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陆军军医大学第二附属医院心血管内科,重庆 400037

骨形态发生蛋白7 慢病毒载体构建 Jagged1 血管钙化

重庆市自然科学基金面上项目陆军军医大学医院青年博士人才孵化计划

CSTB2023NSCQ-MSX06862022YQB029

2024

局解手术学杂志
重庆市解剖学会,第三军医大学

局解手术学杂志

CSTPCD
影响因子:1.063
ISSN:1672-5042
年,卷(期):2024.33(2)
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