Mechanotransduction in the Cardiovascular System: From Developmental Origins to Homeostasis and Pathology

被引:67
作者
Garoffolo, Gloria [1 ,2 ]
Pesce, Maurizio [1 ]
机构
[1] IRCCS, Ctr Cardiol Monzino, Unita Ingn Tissutale Cardiovasc, Via Parea 4, I-20138 Milan, Italy
[2] Univ Milano Bicocca, PhD Program Translat & Mol Med DIMET, I-20126 Milan, Italy
关键词
mechanotransduction; YAP; TAZ; stiffness; fibrosis; stromal cells; VASCULAR SMOOTH-MUSCLE; VALVE INTERSTITIAL-CELLS; SHEAR-STRESS; AORTIC-VALVE; EXTRACELLULAR-MATRIX; MECHANICAL MEMORY; GENE-EXPRESSION; NEURAL CREST; HEART FIELD; FLOW;
D O I
10.3390/cells8121607
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
With the term 'mechanotransduction', it is intended the ability of cells to sense and respond to mechanical forces by activating intracellular signal transduction pathways and the relative phenotypic adaptation. While a known role of mechanical stimuli has been acknowledged for developmental biology processes and morphogenesis in various organs, the response of cells to mechanical cues is now also emerging as a major pathophysiology determinant. Cells of the cardiovascular system are typically exposed to a variety of mechanical stimuli ranging from compression to strain and flow (shear) stress. In addition, these cells can also translate subtle changes in biophysical characteristics of the surrounding matrix, such as the stiffness, into intracellular activation cascades with consequent evolution toward pro-inflammatory/pro-fibrotic phenotypes. Since cellular mechanotransduction has a potential readout on long-lasting modifications of the chromatin, exposure of the cells to mechanically altered environments may have similar persisting consequences to those of metabolic dysfunctions or chronic inflammation. In the present review, we highlight the roles of mechanical forces on the control of cardiovascular formation during embryogenesis, and in the development and pathogenesis of the cardiovascular system.
引用
收藏
页数:19
相关论文
共 148 条
[1]  
Abbruzzese TA, 1998, SURGERY, V124, P328, DOI 10.1067/msy.1998.91338
[2]   Ciliary Polycystin-2 Is a Mechanosensitive Calcium Channel Involved in Nitric Oxide Signaling Cascades [J].
AbouAlaiwi, Wissam A. ;
Takahashi, Maki ;
Mell, Blair R. ;
Jones, Thomas J. ;
Ratnam, Shobha ;
Kolb, Robert J. ;
Nauli, Surya M. .
CIRCULATION RESEARCH, 2009, 104 (07) :860-869
[3]   Patterning of the heart field in the chick [J].
Abu-Issa, Radwan ;
Kirby, Margaret L. .
DEVELOPMENTAL BIOLOGY, 2008, 319 (02) :223-233
[4]   Heart field: From mesoderm to heart tube [J].
Abu-Issa, Radwan ;
Kirby, Margaret L. .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2007, 23 :45-68
[5]  
[Anonymous], 1917, on Growth and Form
[6]   Vascular remodeling is governed by a VEGFR3-dependent fluid shear stress set point [J].
Baeyens, Nicolas ;
Nicoli, Stefania ;
Coon, Brian G. ;
Ross, Tyler D. ;
Van den Dries, Koen ;
Han, Jinah ;
Lauridsen, Holly M. ;
Mejean, Cecile O. ;
Eichmann, Anne ;
Thomas, Jean-Leon ;
Humphrey, Jay D. ;
Schwartz, Martin A. .
ELIFE, 2015, 4 :1-35
[7]   The mechanical memory of lung myofibroblasts [J].
Balestrini, Jenna L. ;
Chaudhry, Sidharth ;
Sarrazy, Vincent ;
Koehler, Anne ;
Hinz, Boris .
INTEGRATIVE BIOLOGY, 2012, 4 (04) :410-421
[8]   Dynamic interactions between myocytes, fibroblasts, and extracellular matrix [J].
Banerjee, Indroneal ;
Yekkala, Krishna ;
Borg, Thomas K. ;
Baudino, Troy A. .
INTERACTIVE AND INTEGRATIVE CARDIOLOGY, 2006, 1080 :76-84
[9]   Early myocardial function affects endocardial cushion development in zebrafish [J].
Bartman, T ;
Walsh, EC ;
Wen, KK ;
McKane, M ;
Ren, JH ;
Alexander, J ;
Rubenstein, PA ;
Stainier, DYR .
PLOS BIOLOGY, 2004, 2 (05) :673-681
[10]  
Beamish JA, 2010, TISSUE ENG PART B-RE, V16, P467, DOI [10.1089/ten.teb.2009.0630, 10.1089/ten.TEB.2009.0630]