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机构地区:[1]南京军区福州总医院(福建医科大学福总临床医学院)血液净化科,福州350025 [2]福建省福州市第二医院,福州350025
出 处:《中国中西医结合肾病杂志》2016年第4期303-306,I0002,共5页Chinese Journal of Integrated Traditional and Western Nephrology
基 金:福建省科技计划重点项目(No.2013Y0069)
摘 要:目的:观察DMP1、E11和Sclerostin在高磷诱导钙化的血管平滑肌细胞(VSMC)中的表达,探讨VSMC钙化的可能机制。方法:组织块贴壁法原代培养VSMC,倒置相差显微镜观察细胞形态及α-SMA免疫组化鉴定;3~8代VSMC用于实验,分为空白对照组、正常磷组和高磷组(Pi分别为0.9、1.3和2.6 mmol/L)。培养第6天,茜素红染色检测钙沉积,RT-PCR或Real-time PCR检测DMP1、E11、Sclerostin mRNA表达,Western Blot检测E11蛋白表达。结果:与空白对照组和正常磷组相比,高磷组VSMC钙盐沉积明显增多;DMP1、E11和Sclerostin mRNA表达明显上调(P〈0.05);E11蛋白表达明显增加(P〈0.05)。结论:骨细胞标志性蛋白DMP1、E11和Sclerostin在高磷诱导钙化的VSMC中表达增加,提示血管钙化过程中VSMC最终向骨细胞样细胞转分化。Objective: To observe the expression of DMP1,E11 and Sclerostin involved inhigh phosphorus induced calcification of vascular smooth muscle cells( VSMC). Methods: The explants derived from thoracic aorta were used for primary culture of VSMC and identification of cells was carried on by morphological identification and direct immunohistochemical staining of α- SMA,Passage 3 to 8 of VSMC were used for experiments. VSMC were divided in three groups: normal control group( Pi 0. 9 mmol / L),normal phosphorus group( Pi 1. 3 mmol / L) and high phosphorus group( Pi 2. 6 mmol / L). Calcium deposition was visualized by Alizarin stain method at day 6. DMP1,E11 and Sclerostin mRNA levels were determined by RT- PCR or Real- Time PCR. E11 expression was semi- quantified by Western Blot. Results: Compared with normal control group and normal phosphorus group,the calcium deposition was increased in high phosphorus group. DMP1,E11 and Sclerostin mRNA expression was significantly increased in high phosphorus group( P 〈0. 05). The expression of E11 in high phosphorus group was significantly increased compared with normal control groupand normal phosphorus group( P〈 0. 05). Conclusion: The increase of expression of DMP1,E11 and Sclerostin in calcified VSMCshowsvascularcalcificationinvolves a VSMCtransition to an osteocyte- like phenotype.
关 键 词:血管钙化血管 平滑肌细胞 DMP1 E11 SCLEROSTIN
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