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球形和全长脂联素对人内皮细胞的保护作用:脂联素诱导血管生成的新见解。

Protective actions of globular and full-length adiponectin on human endothelial cells: novel insights into adiponectin-induced angiogenesis.

作者信息

Adya Raghu, Tan Bee K, Chen Jing, Randeva Harpal S

机构信息

Division of Metabolic and Vascular Health, Warwick Medical School, University of Warwick, Coventry, UK.

出版信息

J Vasc Res. 2012;49(6):534-43. doi: 10.1159/000338279. Epub 2012 Sep 4.

Abstract

BACKGROUND/AIMS: Adiponectin levels are decreased in diabetes and atherosclerosis. Coexisting hyperglycaemia and systemic inflammation predisposes to dysregulated angiogenesis and vascular disease. We investigated the effect of globular adiponectin (gAd) and full-length adiponectin (fAd) on angiogenesis and pro-angiogenic molecules, i.e. matrix metalloproteinase (MMP)-2, MMP-9 and vascular endothelial growth factor (VEGF), in human microvascular endothelial cells (HMEC-1).

METHODS

Angiogenesis was assessed by studying capillary tube formation in HMEC-1 on growth factor-reduced Matrigel. Endothelial cell migration assay was performed in a modified Boyden chamber.

RESULTS

Endothelial cell proliferation, in vitro migration and angiogenesis were significantly increased by gAd (mediated by AdipoR1, AMPK-Akt pathways), and gAd significantly increased MMP-2, MMP-9 and VEGF expression levels. The effect of gAd on VEGF appears to be mediated by AdipoR1, whilst the effect of gAd on MMP-2 and MMP-9 appears to be mediated by AdipoR1 and AdipoR2. Only endothelial cell proliferation was significantly increased by fAd in human microvascular endothelial cells and appears to be mediated by AdipoR2. No significant effects on MMP-2, MMP-9 and VEGF were observed. Importantly, gAd decreased glucose and C-reactive protein-induced angiogenesis with a concomitant reduction in MMP-2, MMP-9 and VEGF in HMEC-1 cells.

CONCLUSION

We report novel insights into the mechanisms of adiponectin on angiogenesis.

摘要

背景/目的:糖尿病和动脉粥样硬化患者体内脂联素水平降低。高血糖与全身炎症并存易导致血管生成失调和血管疾病。我们研究了球形脂联素(gAd)和全长脂联素(fAd)对人微血管内皮细胞(HMEC-1)血管生成及促血管生成分子,即基质金属蛋白酶(MMP)-2、MMP-9和血管内皮生长因子(VEGF)的影响。

方法

通过研究HMEC-1在生长因子减少的基质胶上形成毛细血管管来评估血管生成。在内皮细胞迁移试验中采用改良的博伊登小室。

结果

gAd显著增加内皮细胞增殖、体外迁移和血管生成(由脂联素受体1、AMPK-Akt途径介导),且gAd显著增加MMP-2、MMP-9和VEGF表达水平。gAd对VEGF的作用似乎由脂联素受体1介导,而gAd对MMP-2和MMP-9的作用似乎由脂联素受体1和脂联素受体2介导。在人微血管内皮细胞中,只有fAd显著增加内皮细胞增殖,且似乎由脂联素受体2介导。未观察到对MMP-2、MMP-9和VEGF有显著影响。重要的是,gAd减少了葡萄糖和C反应蛋白诱导的血管生成,同时降低了HMEC-1细胞中MMP-2、MMP-9和VEGF的水平。

结论

我们报道了脂联素对血管生成机制的新见解。

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