scholarly journals Engineering Heart Morphogenesis

2020 ◽  
Vol 38 (8) ◽  
pp. 835-845
Author(s):  
Christian J. Mandrycky ◽  
Nisa P. Williams ◽  
Ivan Batalov ◽  
Danny El-Nachef ◽  
Bernadette S. de Bakker ◽  
...  
Keyword(s):  
2012 ◽  
Vol 5 (1) ◽  
pp. 132-142 ◽  
Author(s):  
Javier T. Granados-Riveron ◽  
J. David Brook

2014 ◽  
Vol 206 (7) ◽  
pp. 909-922 ◽  
Author(s):  
Georg Vogler ◽  
Jiandong Liu ◽  
Timothy W. Iafe ◽  
Ede Migh ◽  
József Mihály ◽  
...  

During heart formation, a network of transcription factors and signaling pathways guide cardiac cell fate and differentiation, but the genetic mechanisms orchestrating heart assembly and lumen formation remain unclear. Here, we show that the small GTPase Cdc42 is essential for Drosophila melanogaster heart morphogenesis and lumen formation. Cdc42 genetically interacts with the cardiogenic transcription factor tinman; with dDAAM which belongs to the family of actin organizing formins; and with zipper, which encodes nonmuscle myosin II. Zipper is required for heart lumen formation, and its spatiotemporal activity at the prospective luminal surface is controlled by Cdc42. Heart-specific expression of activated Cdc42, or the regulatory formins dDAAM and Diaphanous caused mislocalization of Zipper and induced ectopic heart lumina, as characterized by luminal markers such as the extracellular matrix protein Slit. Placement of Slit at the lumen surface depends on Cdc42 and formin function. Thus, Cdc42 and formins play pivotal roles in heart lumen formation through the spatiotemporal regulation of the actomyosin network.


2011 ◽  
Vol 25 (S1) ◽  
Author(s):  
Anastasiia Aleksandrova ◽  
Andras Czirok ◽  
Rusty D Lansford ◽  
Andras Szabo ◽  
Charles D Little ◽  
...  

2021 ◽  
Author(s):  
Christopher J. Derrick ◽  
Eric J. G. Pollitt ◽  
Ashley Sanchez Sevilla Uruchurtu ◽  
Farah Hussein ◽  
Emily S. Noёl

AbstractDuring early vertebrate heart development, the heart transitions from a linear tube to a complex asymmetric structure. This process includes looping of the tube and ballooning of the emerging cardiac chambers, which occur simultaneously with growth of the heart. A key driver of cardiac growth is deployment of cells from the Second Heart Field (SHF) into both poles of the heart, with cardiac morphogenesis and growth intimately linked in heart development. Laminin is a core component of extracellular matrix (ECM) basement membranes, and although mutations in specific laminin subunits are linked with a variety of cardiac abnormalities, including congenital heart disease and dilated cardiomyopathy, no role for laminin has been identified in early vertebrate heart morphogenesis. We identified dynamic, tissue-specific expression of laminin subunit genes in the developing zebrafish heart, supporting a role for laminins in heart morphogenesis.lamb1amutants exhibit cardiomegaly from 2dpf onwards, with subsequent progressive defects in cardiac morphogenesis characterised by a failure of the chambers to compact around the developing atrioventricular canal. We show that loss oflamb1aresults in excess addition of SHF cells to the atrium, revealing that Lamb1a functions to limit heart size during cardiac development by restricting SHF addition to the venous pole.lamb1amutants exhibit hallmarks of altered haemodynamics, and specifically blocking cardiac contractility inlamb1amutants rescues heart size and atrial SHF addition. Furthermore, we identify that FGF and RA signalling, two conserved pathways promoting SHF addition, are regulated by heart contractility and are dysregulated inlamb1amutants, suggesting that laminin mediates interactions between SHF deployment, heart biomechanics, and biochemical signalling during heart development. Together, this describes the first requirement for laminins in early vertebrate heart morphogenesis, reinforcing the importance of specialised ECM composition in cardiac development.


Development ◽  
2011 ◽  
Vol 138 (7) ◽  
pp. 1297-1308 ◽  
Author(s):  
Pari-Sima Müller ◽  
Ramona Schulz ◽  
Silvia Maretto ◽  
Ita Costello ◽  
Shankar Srinivas ◽  
...  

2008 ◽  
Vol 105 (12) ◽  
pp. 4763-4768 ◽  
Author(s):  
N. Sultana ◽  
K. Nag ◽  
K. Hoshijima ◽  
D. W. Laird ◽  
A. Kawakami ◽  
...  
Keyword(s):  

2014 ◽  
Vol 14 (1) ◽  
pp. 10 ◽  
Author(s):  
Inese Cakstina ◽  
Una Riekstina ◽  
Martins Boroduskis ◽  
Ilva Nakurte ◽  
Janis Ancans ◽  
...  

Author(s):  
Stamatiki Katraki-Pavlou ◽  
Pinelopi Kastana ◽  
Dimitris Bousis ◽  
Despoina Ntenekou ◽  
Aimilia Varela ◽  
...  

Protein tyrosine phosphatase receptor zeta 1 (PTPRZ1) is a transmembrane tyrosine phosphatase receptor highly expressed in embryonic stem cells. In the present work, gene expression analyses of Ptprz1-/- and Ptprz1+/+ mice endothelial cells and hearts pointed to an unidentified role of PTPRZ1 in heart development through regulation of heart-specific transcription factor genes. Echocardiography analysis in mice identified that both systolic and diastolic functions are affected in Ptprz1-/- compared to Ptprz1+/+ hearts, based on a dilated LV cavity, decreased ejection fraction and fraction shortening, and increased angiogenesis in Ptprz1-/- hearts, with no signs of cardiac hypertrophy. A zebrafish ptprz1-/- knockout was also generated and exhibits mis-regulated expression of developmental cardiac markers, bradycardia and defective heart morphogenesis characterized by enlarged ventricles and defected contractility. A selective PTPRZ1 tyrosine phosphatase inhibitor affected zebrafish heart development and function in a way like what is observed in the ptprz1-/- zebrafish. The same inhibitor had no effect in the function of the adult zebrafish heart, suggesting that PTPRZ1 is not important for the adult heart function, in line with data from the human cell atlas showing very low to negligible PTPRZ1 expression in the adult human heart. However, in line with the animal models, Ptprz1 was expressed in many different cell types in the human fetal heart, such as valvar, fibroblast-like, cardiomyocytes and endothelial cells. Collectively, these data suggest that PTPRZ1 regulates cardiac morphogenesis in a way that subsequently affects heart function and warrant further studies for the involvement of PTPRZ1 in idiopathic congenital cardiac pathologies.


2004 ◽  
Vol 114 (5) ◽  
pp. 517-519 ◽  
Author(s):  
Claudia Sandri ◽  
Raffaella Di Lisi ◽  
Anne Picard ◽  
Carla Argentini ◽  
Elisa Calabria ◽  
...  

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