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冠状动脉内皮中的血管生成素-酪氨酸激酶2系统可防止氧化型低密度脂蛋白诱导的细胞凋亡。

The angiopoietin-tie2 system in coronary artery endothelium prevents oxidized low-density lipoprotein-induced apoptosis.

作者信息

Kim I, Moon S O, Han C Y, Pak Y K, Moon S K, Kim J J, Koh G Y

机构信息

National Creative Research Initiatives Center for Cardiac Regeneration and Institute of Cardiovascular Research, Chonbuk University School of Medicine, Chonju, South Korea.

出版信息

Cardiovasc Res. 2001 Mar;49(4):872-81. doi: 10.1016/s0008-6363(00)00295-9.

Abstract

OBJECTIVES

A healthy, intact coronary artery endothelium is important because most common coronary artery diseases result from loss of endothelial integrity. In this study, we explored the biological significance of the angiopoietin-Tie2 system in porcine coronary artery.

METHODS

Cultured porcine coronary artery endothelial cells and explanted coronary arteries were used.

RESULTS

Immunohistochemical analyses indicated that Ang1 is selectively expressed in vascular muscular cells, whereas angiopoietin-2 (Ang2) and Tie2 are selectively expressed in endothelial cells. Accordingly, Ang1 mRNA is mainly expressed in cultured porcine coronary artery vascular smooth muscle cells, whereas Ang2 and Tie2 mRNAs are mainly expressed in cultured porcine coronary artery endothelial cells (PCAECs). Ang1 (200 ng/ml) induced Tie2 phosphorylation, while Ang2 (200 ng/ml) did not produce Tie2 phosphorylation. Ang1 increased the survival of cultured PCAECs during apoptosis induced by oxidized low-density lipoprotein (OxLDL). This survival effect was does-dependent and PI. Furthermore, Ang1 also protected endothelial cells of explanted coronary artery against OxLDL-induced apoptosis artery.

CONCLUSION

These results suggest that adult coronary artery contains Ang1-Tie2 components that enhance endothelial cell survival to help maintain the normal integrity of the coronary artery endothelium.

摘要

目的

健康、完整的冠状动脉内皮很重要,因为大多数常见的冠状动脉疾病都是由内皮完整性丧失所致。在本研究中,我们探讨了血管生成素-Tie2系统在猪冠状动脉中的生物学意义。

方法

使用培养的猪冠状动脉内皮细胞和离体冠状动脉。

结果

免疫组织化学分析表明,血管生成素1(Ang1)在血管平滑肌细胞中选择性表达,而血管生成素2(Ang2)和Tie2在内皮细胞中选择性表达。相应地,Ang1信使核糖核酸(mRNA)主要在培养的猪冠状动脉血管平滑肌细胞中表达,而Ang2和Tie2的mRNA主要在培养的猪冠状动脉内皮细胞(PCAECs)中表达。Ang1(200纳克/毫升)诱导Tie2磷酸化,而Ang2(200纳克/毫升)未引起Tie2磷酸化。在氧化型低密度脂蛋白(OxLDL)诱导的凋亡过程中,Ang1提高了培养的PCAECs的存活率。这种存活效应呈剂量依赖性且与磷脂酰肌醇-3激酶(PI)有关。此外,Ang1还保护离体冠状动脉的内皮细胞免受OxLDL诱导的凋亡。

结论

这些结果表明,成年冠状动脉含有Ang1-Tie2成分,可增强内皮细胞存活,有助于维持冠状动脉内皮的正常完整性。

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