Open Access
CC BY-NC 4.0 · Arch Plast Surg 2022; 49(01): 115-120
DOI: 10.5999/aps.2021.00626
Research/Experimental
Original Article

Wall shear stress on vascular smooth muscle cells exerts angiogenic effects on extracranial arteriovenous malformations

Department of Plastic and Reconstructive Surgery, School of Medicine, Kyungpook National University, Daegu, Korea
,
Department of Plastic and Reconstructive Surgery, School of Medicine, Kyungpook National University, Daegu, Korea
,
Department of Plastic and Reconstructive Surgery, School of Medicine, Kyungpook National University, Daegu, Korea
,
Department of Plastic and Reconstructive Surgery, School of Medicine, Kyungpook National University, Daegu, Korea
Cell and Matrix Research Institute, School of Medicine, Kyungpook National University, Daegu, Korea
,
Department of Plastic and Reconstructive Surgery, School of Medicine, Kyungpook National University, Daegu, Korea
Cell and Matrix Research Institute, School of Medicine, Kyungpook National University, Daegu, Korea
,
Department of Dermatology, School of Medicine, Kyungpook National University, Daegu, Korea
,
Department of Radiology, School of Medicine, Kyungpook National University, Daegu, Korea
,
Department of Radiology, School of Medicine, Kyungpook National University, Daegu, Korea
,
Department of Surgery, School of Medicine, Kyungpook National University, Daegu, Korea
,
Department of Pediatrics, School of Medicine, Kyungpook National University, Daegu, Korea
,
School of Business Administration, Kyungpook National University, Daegu, Korea
,
Department of Plastic and Reconstructive Surgery, School of Medicine, Kyungpook National University, Daegu, Korea
Cell and Matrix Research Institute, School of Medicine, Kyungpook National University, Daegu, Korea
› Author Affiliations
Preview

Background In addition to vascular endothelial cells, vascular smooth muscle cells (VSMCs) are subject to continuous shear stress because of blood circulation. The angiogenic properties of VSMCs in extracranial arteriovenous malformations (AVMs) may exceed those of normal blood vessels if the body responds more sensitively to mechanical stimuli. This study was performed to investigate the hypothesis that rapid angiogenesis may be achieved by mechanical shear stress.

Methods VSMCs were obtained from six patients who had AVMs and six normal controls. The target genes were set to angiopoietin-2 (AGP2), aquaporin-1 (AQP1), and transforming growth factor-beta receptor 1 (TGFBR1). Reverse-transcriptase polymerase chain reaction (RT-PCR) and real-time PCR were implemented to identify the expression levels for target genes. Immunofluorescence was also conducted.

Results Under the shear stress condition, mean relative quantity values of AGP2, AQP1, and TGFBR1 in AVM tissues were 1.927±0.528, 1.291±0.031, and 2.284±1.461 when compared with neutral conditions. The expression levels of all three genes in AVMs were higher than those in normal tissue except for AQP1 under shear stress conditions. Immunofluorescence also revealed increased staining of shear stress-induced genes in the normal tissue and in AVM tissue.

Conclusions Shear stress made the VSMCs of AVMs more sensitive. Although the pathogenesis of AVMs remains unclear, our study showed that biomechanical stimulation imposed by shear stress may aggravate angiogenesis in AVMs.

This work was supported by Biomedical Research Institute Grant, Kyungpook National University Hospital (2019).




Publication History

Received: 10 May 2021

Accepted: 30 August 2021

Article published online:
02 June 2022

© 2022. The Korean Society of Plastic and Reconstructive Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonCommercial License, permitting unrestricted noncommercial use, distribution, and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes. (https://creativecommons.org/licenses/by-nc/4.0/)

Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA