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 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
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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. |
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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. – sequence: 3 givenname: Nancy surname: Webb middlename: R. fullname: Webb, Nancy R. – sequence: 4 givenname: Lisa surname: Cassis middlename: A. fullname: Cassis, Lisa A. – sequence: 5 givenname: Alan surname: Daugherty fullname: Daugherty, Alan – sequence: 6 givenname: Hong surname: Lu middlename: S. fullname: Lu, Hong S. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32101472$$D View this record in MEDLINE/PubMed |
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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 |
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