The Role of Macrophages in Aortic Dissection
Aortic dissection (AD) is a fatal disease that accounts for a large proportion of aortic-related deaths and has an incidence of about 3–4 per 100,000 individuals every year. Recent studies have found that inflammation plays an important role in the development of AD, and that macrophages are the hub...
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doaj-753f64c65e3245ab9f3bf390e792b28e2020-11-25T02:18:54ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2020-02-011110.3389/fphys.2020.00054494621The Role of Macrophages in Aortic DissectionXinhao Wang0Hongpeng Zhang1Long Cao2Long Cao3Yuan He4Airong Ma5Wei Guo6Department of Vascular and Endovascular Surgery, The First Medical Center of Chinese PLA General Hospital, Beijing, ChinaDepartment of Vascular and Endovascular Surgery, The First Medical Center of Chinese PLA General Hospital, Beijing, ChinaDepartment of Vascular and Endovascular Surgery, The First Medical Center of Chinese PLA General Hospital, Beijing, ChinaDepartment of General Surgery, PLA No. 983 Hospital, Tianjin, ChinaDepartment of Vascular and Endovascular Surgery, The First Medical Center of Chinese PLA General Hospital, Beijing, ChinaDepartment of Obstetrics, Zibo Central Hospital, Zibo, ChinaDepartment of Vascular and Endovascular Surgery, The First Medical Center of Chinese PLA General Hospital, Beijing, ChinaAortic dissection (AD) is a fatal disease that accounts for a large proportion of aortic-related deaths and has an incidence of about 3–4 per 100,000 individuals every year. Recent studies have found that inflammation plays an important role in the development of AD, and that macrophages are the hub of inflammation in the aortic wall. Aortic samples from AD patients reveal a large amount of macrophage infiltration. The sites of macrophage infiltration and activity vary throughout the different stages of AD, with involvement even in the tissue repair phase of AD. Angiotensin II has been shown to be an important factor in the stimulation of macrophage activity. Stimulated macrophages can secrete metalloproteinases, inflammatory factors and other substances to cause matrix destruction, smooth muscle cell apoptosis, neovascularization and more, all of which destroy the aortic wall structure. At the same time, there are a number of factors that regulate macrophages to reduce the formation of AD and induce the repair of torn aortic tissues. The aim of this review is to take a close look at the roles of macrophages throughout the course of AD disease.https://www.frontiersin.org/article/10.3389/fphys.2020.00054/fullaortic dissectionmacrophageinflammationAng IIaortic wall |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xinhao Wang Hongpeng Zhang Long Cao Long Cao Yuan He Airong Ma Wei Guo |
spellingShingle |
Xinhao Wang Hongpeng Zhang Long Cao Long Cao Yuan He Airong Ma Wei Guo The Role of Macrophages in Aortic Dissection Frontiers in Physiology aortic dissection macrophage inflammation Ang II aortic wall |
author_facet |
Xinhao Wang Hongpeng Zhang Long Cao Long Cao Yuan He Airong Ma Wei Guo |
author_sort |
Xinhao Wang |
title |
The Role of Macrophages in Aortic Dissection |
title_short |
The Role of Macrophages in Aortic Dissection |
title_full |
The Role of Macrophages in Aortic Dissection |
title_fullStr |
The Role of Macrophages in Aortic Dissection |
title_full_unstemmed |
The Role of Macrophages in Aortic Dissection |
title_sort |
role of macrophages in aortic dissection |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Physiology |
issn |
1664-042X |
publishDate |
2020-02-01 |
description |
Aortic dissection (AD) is a fatal disease that accounts for a large proportion of aortic-related deaths and has an incidence of about 3–4 per 100,000 individuals every year. Recent studies have found that inflammation plays an important role in the development of AD, and that macrophages are the hub of inflammation in the aortic wall. Aortic samples from AD patients reveal a large amount of macrophage infiltration. The sites of macrophage infiltration and activity vary throughout the different stages of AD, with involvement even in the tissue repair phase of AD. Angiotensin II has been shown to be an important factor in the stimulation of macrophage activity. Stimulated macrophages can secrete metalloproteinases, inflammatory factors and other substances to cause matrix destruction, smooth muscle cell apoptosis, neovascularization and more, all of which destroy the aortic wall structure. At the same time, there are a number of factors that regulate macrophages to reduce the formation of AD and induce the repair of torn aortic tissues. The aim of this review is to take a close look at the roles of macrophages throughout the course of AD disease. |
topic |
aortic dissection macrophage inflammation Ang II aortic wall |
url |
https://www.frontiersin.org/article/10.3389/fphys.2020.00054/full |
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