Aortic Aneurysms and Dissections Series

The aortic wall is composed of highly dynamic cell populations and extracellular matrix. In response to changes in the biomechanical environment, aortic cells and extracellular matrix modulate their structure and functions to increase aortic wall strength and meet the hemodynamic demand. Compromise...

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Published in:Arteriosclerosis, thrombosis, and vascular biology Vol. 40; no. 3; pp. e37 - e46
Main Authors: Shen, Ying H., LeMaire, Scott A., Webb, Nancy R., Cassis, Lisa A., Daugherty, Alan, Lu, Hong S.
Format: Journal Article
Language:English
Published: United States American Heart Association, Inc 01-03-2020
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Abstract The aortic wall is composed of highly dynamic cell populations and extracellular matrix. In response to changes in the biomechanical environment, aortic cells and extracellular matrix modulate their structure and functions to increase aortic wall strength and meet the hemodynamic demand. Compromise in the structural and functional integrity of aortic components leads to aortic degeneration, biomechanical failure, and the development of aortic aneurysms and dissections (AAD). A better understanding of the molecular pathogenesis of AAD will facilitate the development of effective medications to treat these conditions. Here, we summarize recent findings on AAD published in ATVB. In this issue, we focus on the dynamics of aortic cells and extracellular matrix in AAD; in the next issue, we will focus on the role of signaling pathways in AAD.
AbstractList The aortic wall is composed of highly dynamic cell populations and extracellular matrix. In response to changes in the biomechanical environment, aortic cells and extracellular matrix modulate their structure and functions to increase aortic wall strength and meet the hemodynamic demand. Compromise in the structural and functional integrity of aortic components leads to aortic degeneration, biomechanical failure, and the development of aortic aneurysms and dissections (AAD). A better understanding of the molecular pathogenesis of AAD will facilitate the development of effective medications to treat these conditions. Here, we summarize recent findings on AAD published in ATVB. In this issue, we focus on the dynamics of aortic cells and extracellular matrix in AAD; in the next issue, we will focus on the role of signaling pathways in AAD.
The aortic wall is composed of highly dynamic cell populations and extracellular matrix. In response to changes in the biomechanical environment, aortic cells and extracellular matrix modulate their structure and functions to increase aortic wall strength and meet the hemodynamic demand. Compromise in the structural and functional integrity of aortic components leads to aortic degeneration, biomechanical failure, and the development of aortic aneurysms and dissections (AAD). A better understanding of the molecular pathogenesis of AAD will facilitate the development of effective medications to treat these conditions. Here, we summarize recent findings on AAD published in . In this issue, we focus on the dynamics of aortic cells and extracellular matrix in AAD; in the next issue, we will focus on the role of signaling pathways in AAD.
The aortic wall is composed of highly dynamic cell populations and extracellular matrix. In response to changes in the biomechanical environment, aortic cells and extracellular matrix modulate their structure and functions to increase aortic wall strength and meet the hemodynamic demand. Compromise in the structural and functional integrity of aortic components leads to aortic degeneration, biomechanical failure, and the development of aortic aneurysms and dissections (AAD). A better understanding of the molecular pathogenesis of AAD will facilitate the development of effective medications to treat these conditions. Here, we summarize recent findings on AAD published in ATVB . In this issue, we focus on the dynamics of aortic cells and extracellular matrix in AAD; in the next issue, we will focus on the role of signaling pathways in AAD.
Author Lu, Hong S.
LeMaire, Scott A.
Cassis, Lisa A.
Daugherty, Alan
Webb, Nancy R.
Shen, Ying H.
AuthorAffiliation From the Division of Cardiothoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX (Y.H.S., S.A.L.) Department of Cardiovascular Surgery, Texas Heart Institute, Houston (Y.H.S., S.A.L.) Department of Physiology and Saha Cardiovascular Research Center (A.D., H.S.L.), University of Kentucky, Lexington. Department of Pharmacology and Nutritional Sciences (N.R.W., L.A.C.), University of Kentucky, Lexington
AuthorAffiliation_xml – name: From the Division of Cardiothoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX (Y.H.S., S.A.L.) Department of Cardiovascular Surgery, Texas Heart Institute, Houston (Y.H.S., S.A.L.) Department of Physiology and Saha Cardiovascular Research Center (A.D., H.S.L.), University of Kentucky, Lexington. Department of Pharmacology and Nutritional Sciences (N.R.W., L.A.C.), University of Kentucky, Lexington
Author_xml – sequence: 1
  givenname: Ying
  surname: Shen
  middlename: H.
  fullname: Shen, Ying H.
  organization: From the Division of Cardiothoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX (Y.H.S., S.A.L.) Department of Cardiovascular Surgery, Texas Heart Institute, Houston (Y.H.S., S.A.L.) Department of Physiology and Saha Cardiovascular Research Center (A.D., H.S.L.), University of Kentucky, Lexington. Department of Pharmacology and Nutritional Sciences (N.R.W., L.A.C.), University of Kentucky, Lexington
– sequence: 2
  givenname: Scott
  surname: LeMaire
  middlename: A.
  fullname: LeMaire, Scott A.
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  givenname: Nancy
  surname: Webb
  middlename: R.
  fullname: Webb, Nancy R.
– sequence: 4
  givenname: Lisa
  surname: Cassis
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  fullname: Cassis, Lisa A.
– sequence: 5
  givenname: Alan
  surname: Daugherty
  fullname: Daugherty, Alan
– sequence: 6
  givenname: Hong
  surname: Lu
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  fullname: Lu, Hong S.
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32101472$$D View this record in MEDLINE/PubMed
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Keywords proteoglycans
aortic aneurysm
muscles
inflammation
extracellular matrix
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Snippet The aortic wall is composed of highly dynamic cell populations and extracellular matrix. In response to changes in the biomechanical environment, aortic cells...
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SubjectTerms Aneurysm, Dissecting - metabolism
Aneurysm, Dissecting - pathology
Aneurysm, Dissecting - physiopathology
Animals
Aorta - metabolism
Aorta - pathology
Aorta - physiopathology
Aortic Aneurysm - metabolism
Aortic Aneurysm - pathology
Aortic Aneurysm - physiopathology
Dilatation, Pathologic
Endothelial Cells - metabolism
Endothelial Cells - pathology
Extracellular Matrix - metabolism
Extracellular Matrix - pathology
Fibroblasts - metabolism
Fibroblasts - pathology
Hemodynamics
Humans
Muscle, Smooth, Vascular - metabolism
Muscle, Smooth, Vascular - pathology
Muscle, Smooth, Vascular - physiopathology
Myocytes, Smooth Muscle - metabolism
Myocytes, Smooth Muscle - pathology
Vascular Remodeling
Title Aortic Aneurysms and Dissections Series
URI http://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00043605-202003000-00001
https://www.ncbi.nlm.nih.gov/pubmed/32101472
https://search.proquest.com/docview/2366631753
Volume 40
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