Quantitative 4D imaging of biomechanical regulation of ventricular growth and maturation

被引:2
作者
Cho, Jae Min [1 ,2 ]
Poon, Mong Lung Steve [1 ,3 ]
Zhu, Enbo [1 ,2 ]
Wang, Jing
Butcher, Jonathan T. [3 ,4 ]
Hsiai, Tzung [1 ,2 ,4 ]
机构
[1] Div Cardiol, Dept Med, UCLA, David Geffen Schoolof Med, Los Angeles, CA 90095 USA
[2] Greater Angeles VA Healthcare Syst, Dept Med, Los Angeles, CA 90073 USA
[3] Cornell Univ, Nancy E & Peter C Meinig Sch Biomed Engn, Ithaca, NY USA
[4] UCLA, Dept Bioengn, Los Angeles, CA 90095 USA
关键词
Ultrasound; Hemodynamics; Trabeculation; Light sheet Micro-CT; CARDIAC DEVELOPMENT; NOTCH; ZEBRAFISH; NONCOMPACTION; DYNAMICS; INJURY;
D O I
10.1016/j.cobme.2022.100438
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Abnormal cardiac development is intimately associated with congenital heart disease. During development, a sponge-like network of muscle fibers in the endocardium, known as trabeculation, becomes compacted. Biomechanical forces regulate myocardial differentiation and proliferation to form trabeculation, while the molecular mechanism is still enigmatic. Biomechanical forces, including intracardiac hemodynamic flow and myocardial contractile force, activate a host of mo-lecular signaling pathways to mediate cardiac morphogenesis. While mechanotransduction pathways to initiate ventricular trabeculation is well studied, deciphering the relative impor-tance of hemodynamic shear vs. mechanical contractile forces to modulate the transition from trabeculation to compaction requires advanced imaging tools and genetically tractable animal models. For these reasons, the advent of 4D multi -scale light-sheet imaging and complementary multiplex live imaging via micro-CT in the beating zebrafish heart and live chick embryos, respectively. Thus, this review highlights the complementary animal models and advanced imaging needed to elucidate the mechanotransduction underlying cardiac ventricular development.
引用
收藏
页数:12
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