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振荡剪切应力促进动静脉畸形血管内皮细胞的血管生成作用。

Oscillatory shear stress promotes angiogenic effects in arteriovenous malformations endothelial cells.

机构信息

Department of Plastic and Reconstructive Surgery, School of Medicine, Kyungpook National University, 130 Dongdeok-ro, Jung-gu, Daegu, 41944, Korea.

Cell & Matrix Research Institute, School of Medicine, Kyungpook National University, 130 Dongdeok-ro, Jung-gu, Daegu, 41944, Korea.

出版信息

Mol Med. 2021 Mar 31;27(1):31. doi: 10.1186/s10020-021-00291-6.

Abstract

BACKGROUND

Vascular endothelial cells (ECs) are subject to continuous shear stress due to blood circulation. Mechanical stress due to high shear flow can also cause arteriovenous malformation (AVM) when ECs respond hyper-sensitively to shear flow. This study was conducted to test the hypothesis that angiogenesis could be promoted in response to mechanical stress via regulation of pro-angiogenic factors in AVM cells.

METHODS

ECs were extracted from the tissue samples from six AVM patients and six normal patients. Shear stress at 7 dynes/cm2 were applied for 24 h. Before and after application of shear stress to each group, RT-PCR was performed to access the expression levels of angiopoietin2(AGP2), aquaporin1(AQP1) and TGFβR1. Immunofluorescences was also performed to evaluate the level of protein expressions.

RESULTS

In both normal and AVM tissues, AGP2 and TGFβR1 under the shear stress showed increased expression in the ECs compared to the non-sheared samples. When AVMs and normal arterial vasculature were compared, the expression levels of both AGP2 and TGFβR1 in AVMs were higher when compared to normal arterial vasculature with or without shear stress. Immunofluorescence-based protein analysis also confirmed shear-induced AGP2 and TGFβR1 in both samples of normal and AVM patients.

CONCLUSIONS

AVMs exhibited higher sensitivity to shear stress by producing higher expressions of some marked genes and proteins that regulate the endothelial functions upon exposure to shear stress. While the physiological mechanism for AVMs remain elusive, our study shows the plausibility of physical stress imposed by the shearing flow can cause the occurrence of AVMs.

摘要

背景

由于血液循环,血管内皮细胞(EC)持续受到切变应力。当 EC 对切变流过度敏感时,高切变流产生的机械应力也会导致动静脉畸形(AVM)。本研究旨在通过调节 AVM 细胞中的促血管生成因子,检验机械应力可促进血管生成的假说。

方法

从 6 名 AVM 患者和 6 名正常患者的组织样本中提取 EC。施加 7 dynes/cm2 的切变应力 24 h。在对每组施加切变应力之前和之后,进行 RT-PCR 以评估血管生成素 2(AGP2)、水通道蛋白 1(AQP1)和 TGFβR1 的表达水平。还进行了免疫荧光染色以评估蛋白表达水平。

结果

在正常和 AVM 组织中,与未受切变的样本相比,切变应力下的 AGP2 和 TGFβR1 在 EC 中的表达增加。当将 AVM 和正常动脉血管进行比较时,与正常动脉血管相比,无论是否施加切变应力,AGP2 和 TGFβR1 的表达水平在 AVM 中均更高。基于免疫荧光的蛋白分析也证实了正常和 AVM 患者样本中切变诱导的 AGP2 和 TGFβR1。

结论

AVM 通过产生更高表达某些调节内皮功能的标记基因和蛋白来对切变应力表现出更高的敏感性。虽然 AVM 的生理机制尚不清楚,但我们的研究表明,切变流施加的物理应激可能导致 AVM 的发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f86e/8011119/2f06e84aecb5/10020_2021_291_Fig1_HTML.jpg

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