The harder the climb the better the view: The impact of substrate stiffness on cardiomyocyte fate

被引:13
|
作者
Querceto, Silvia [1 ]
Santoro, Rosaria [2 ,3 ]
Gowran, Aoife [2 ]
Grandinetti, Bruno [4 ]
Pompilio, Giulio [2 ,5 ]
Regnier, Michael [6 ]
Tesi, Chiara [1 ]
Poggesi, Corrado [1 ]
Ferrantini, Cecilia [1 ]
Pioner, Jose Manuel [7 ]
机构
[1] Univ Firenze, Dept Expt & Clin Med, Div Physiol, Florence, Italy
[2] Ctr Cardiol Monzino IRCCS, Unita Biol Vascolare & Med Rigenerat, Via Carlo Parea 4, Milan, Italy
[3] Politecn Milan, Dept Elect Informat & Biomed Engn, Milan, Italy
[4] European Lab Nonlinear Spect LENS, Sesto Fiorentino, FI, Italy
[5] Univ Milan, Dept Biomed Surg & Dent Sci, Milan, Italy
[6] Univ Washington, Dept Bioengn, Seattle, WA 98195 USA
[7] Univ Firenze, Dept Biol, Florence, Italy
关键词
Substrate stiffness  hiPSC; Cardiomyocytes; Cardiac extracellular matrix; Tissue engineering; Genetic cardiomyopathy; CELL-DERIVED CARDIOMYOCYTES; EXTRACELLULAR-MATRIX; SKELETAL-MUSCLE; STEM-CELLS; TITIN ISOFORM; NEONATAL CARDIOMYOCYTES; CARDIAC DIFFERENTIATION; MYOCARDIAL STIFFNESS; MECHANICAL-STRESS; HEART;
D O I
10.1016/j.yjmcc.2022.02.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The quest for novel methods to mature human induced pluripotent stem cell-derived cardiomyocytes (hiPSCCMs) for cardiac regeneration, modelling and drug testing has emphasized a need to create microenvironments with physiological features. Many studies have reported on how cardiomyocytes sense substrate stiffness and adapt their morphological and functional properties. However, these observations have raised new biological questions and a shared vision to translate it into a tissue or organ context is still elusive. In this review, we will focus on the relevance of substrates mimicking cardiac extracellular matrix (cECM) rigidity for the understanding of the biomechanical crosstalk between the extracellular and intracellular environment. The ability to opportunely modulate these pathways could be a key to regulate in vitro hiPSC-CM maturation. Therefore, both hiPSCCM models and substrate stiffness appear as intriguing tools for the investigation of cECM-cell interactions. More understanding of these mechanisms may provide novel insights on how cECM affects cardiac cell function in the context of genetic cardiomyopathies.
引用
收藏
页码:36 / 49
页数:14
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