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Notch1-RBP-Jk/Msx2 信号通路在糖尿病肾病大鼠主动脉钙化中的作用。

The Involvement of Notch1-RBP-Jk/Msx2 Signaling Pathway in Aortic Calcification of Diabetic Nephropathy Rats.

机构信息

Department of Nephrology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, China.

Department of Nephrology, Luzhou People's Hospital, Luzhou, Sichuan 646000, China.

出版信息

J Diabetes Res. 2017;2017:8968523. doi: 10.1155/2017/8968523. Epub 2017 Dec 31.

Abstract

BACKGROUND

This study explored the changes in expression of vascular smooth muscle cell (VSMC) markers and osteogenic markers, as well as the involvement of Notch1-RBP-Jk/Msx2 pathway in a rat model of diabetic nephropathy (DN) with vascular calcification.

METHODS

A rat model of DN with concomitant vascular calcification was created by intraperitoneal injection of streptozotocin followed by administration of vitamin D3 and nicotine. Biochemical analysis and histological examination of aortic tissue were performed. VSMC markers and osteogenic markers as well as target molecules in Notch1-RBP-Jk/Msx2 were determined by quantitative real-time polymerase chain reaction and immunohistochemical analysis.

RESULTS

Serum calcium and phosphorus levels were significantly increased in model rats as compared to that in normal controls. Diabetic rats with vascular calcification exhibited mineral deposits in aortic intima-media accompanied by decreased expression of VSMC markers and increased expression of osteogenic markers. Notch1, RBP-Jk, Msx2, Jagged1, and N1-ICD were barely expressed in the aortic wall of normal rats. In contrast, these were significantly increased in the model group at all time points (8, 12, and 16 weeks), as compared to that in the normal rats.

CONCLUSION

Activation of the Notch1-RBP-Jk/Msx2 signaling pathway may be involved in the development and progression of vascular calcification in DN.

摘要

背景

本研究探讨了血管平滑肌细胞(VSMC)标志物和成骨标志物表达的变化,以及 Notch1-RBP-Jk/Msx2 通路在糖尿病肾病(DN)伴血管钙化大鼠模型中的作用。

方法

通过腹腔注射链脲佐菌素,随后给予维生素 D3 和尼古丁,建立伴有血管钙化的糖尿病肾病大鼠模型。对主动脉组织进行生化分析和组织学检查。通过实时定量聚合酶链反应和免疫组织化学分析,测定 VSMC 标志物和成骨标志物以及 Notch1-RBP-Jk/Msx2 中的靶分子。

结果

与正常对照组相比,模型组大鼠血清钙、磷水平明显升高。伴有血管钙化的糖尿病大鼠主动脉内膜-中膜出现矿化沉积,VSMC 标志物表达减少,成骨标志物表达增加。正常大鼠主动脉壁中 Notch1、RBP-Jk、Msx2、Jagged1 和 N1-ICD 的表达几乎检测不到。相反,在所有时间点(8、12 和 16 周),模型组的表达均明显高于正常组。

结论

Notch1-RBP-Jk/Msx2 信号通路的激活可能参与了糖尿病肾病血管钙化的发生和发展。

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