Multifunctional Role of Chymase in Acute and Chronic Tissue Injury and Remodeling

被引:86
作者
Dell'Italia, Louis J. [1 ,2 ]
Collawn, James F. [3 ]
Ferrario, Carlos M. [4 ]
机构
[1] Univ Alabama Birmingham, Dept Med, Div Cardiol, Birmingham Vet Affairs Med Ctr, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Med, Div Cardiovasc Dis, Birmingham, AL 35294 USA
[3] Univ Alabama, Dept Cell Dev & Integrat Biol, Tuscaloosa, AL USA
[4] Wake Forest Univ, Sch Med, Div Surg Sci, Winston Salem, NC 27109 USA
基金
美国国家卫生研究院;
关键词
angiotensin II; chymases; endothelial cells; mast cells; renin; MAST-CELL CHYMASE; ANGIOTENSIN-CONVERTING-ENZYME; ISOLATED MITRAL REGURGITATION; ABDOMINAL AORTIC-ANEURYSM; II-FORMING PATHWAYS; DEPENDENT MATRIX-METALLOPROTEINASE-9 ACTIVATION; LEFT-VENTRICULAR DYSFUNCTION; PREVENTS CARDIAC FIBROSIS; DIPEPTIDYL PEPTIDASE-I; MYOCARDIAL-INFARCTION;
D O I
10.1161/CIRCRESAHA.117.310978
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Chymase is the most efficient Ang II (angiotensin II)-forming enzyme in the human body and has been implicated in a wide variety of human diseases that also implicate its many other protease actions. Largely thought to be the product of mast cells, the identification of other cellular sources including cardiac fibroblasts and vascular endothelial cells demonstrates a more widely dispersed production and distribution system in various tissues. Furthermore, newly emerging evidence for its intracellular presence in cardiomyocytes and smooth muscle cells opens an entirely new compartment of chymase-mediated actions that were previously thought to be limited to the extracellular space. This review illustrates how these multiple chymase-mediated mechanisms of action can explain the residual risk in clinical trials of cardiovascular disease using conventional renin-angiotensin system blockade.
引用
收藏
页码:319 / 336
页数:18
相关论文
共 252 条
[1]
Identification and characterization of a functional mitochondrial angiotensin system [J].
Abadir, Peter M. ;
Foster, D. Brian ;
Crow, Michael ;
Cooke, Carol A. ;
Rucker, Jasma J. ;
Jain, Alka ;
Smith, Barbara J. ;
Burks, Tyesha N. ;
Cohn, Ronald D. ;
Fedarko, Neal S. ;
Carey, Robert M. ;
O'Rourke, Brian ;
Walston, Jeremy D. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (36) :14849-14854
[2]
Chymase-Dependent Generation of Angiotensin II from Angiotensin-(1-12) in Human Atrial Tissue [J].
Ahmad, Sarfaraz ;
Simmons, Tony ;
Varagic, Jasmina ;
Moniwa, Norihito ;
Chappell, Mark C. ;
Ferrario, Carlos M. .
PLOS ONE, 2011, 6 (12)
[3]
Uptake and Metabolism of the Novel Peptide Angiotensin-(1-12) by Neonatal Cardiac Myocytes [J].
Ahmad, Sarfaraz ;
Varagic, Jasmina ;
Westwood, Brian M. ;
Chappell, Mark C. ;
Ferrario, Carlos M. .
PLOS ONE, 2011, 6 (01)
[4]
Do Plaques Rapidly Progress Prior to Myocardial Infarction? The Interplay Between Plaque Vulnerability and Progression [J].
Ahmadi, Amir ;
Leipsic, Jonathon ;
Blankstein, Ron ;
Taylor, Carolyn ;
Hecht, Harvey ;
Stone, Gregg W. ;
Narula, Jagat .
CIRCULATION RESEARCH, 2015, 117 (01) :99-104
[5]
Ahmed M, 2011, J AM COLL CARDIOL, V55, P671
[6]
Disruption of desmin-mitochondrial architecture in patients with regurgitant mitral valves and preserved ventricular function [J].
Ahmed, Mustafa I. ;
Guichard, Jason L. ;
Rajasekaran, Namakkal S. ;
Ahmad, Shama ;
Mariappan, Nithya ;
Litovsky, Silvio ;
Gupta, Himanshu ;
Lloyd, Steven G. ;
Denney, Thomas S. ;
Powell, Pamela Cox ;
Aban, Inmaculada ;
Collawn, James F. ;
Davies, James E. ;
McGiffin, David C. ;
Dell'Italia, Louis J. .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2016, 152 (04) :1059-+
[7]
Mast cell chymase reduces the toxicity of Gila monster venom, scorpion venom, and vasoactive intestinal polypeptide in mice [J].
Akahoshi, Mitsuteru ;
Song, Chang Ho ;
Piliponsky, Adrian M. ;
Metz, Martin ;
Guzzetta, Andrew ;
Abrink, Magnus ;
Schlenner, Susan M. ;
Feyerabend, Thorsten B. ;
Rodewald, Hans-Reimer ;
Pejler, Gunnar ;
Tsai, Mindy ;
Galli, Stephen J. .
JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (10) :4180-4191
[8]
Differences in tissue angiotensin II-forming pathways by species and organs in vitro [J].
Akasu, M ;
Urata, H ;
Kinoshita, A ;
Sasaguri, M ;
Ideishi, M ;
Arakawa, K .
HYPERTENSION, 1998, 32 (03) :514-520
[9]
ANGIOGRAPHIC PROGRESSION OF CORONARY-ARTERY DISEASE AND THE DEVELOPMENT OF MYOCARDIAL-INFARCTION [J].
AMBROSE, JA ;
TANNENBAUM, MA ;
ALEXOPOULOS, D ;
HJEMDAHLMONSEN, CE ;
LEAVY, J ;
WEISS, M ;
BORRICO, S ;
GORLIN, R ;
FUSTER, V .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1988, 12 (01) :56-62
[10]
Andoh A, 2006, ONCOL REP, V16, P103