Faculty Opinions recommendation of HCN4 dynamically marks the first heart field and conduction system precursors.

Author(s):  
Glenn Fishman ◽  
Karen Maass
2013 ◽  
Vol 113 (4) ◽  
pp. 399-407 ◽  
Author(s):  
Xingqun Liang ◽  
Gang Wang ◽  
Lizhu Lin ◽  
Jennifer Lowe ◽  
Qingquan Zhang ◽  
...  

2017 ◽  
Author(s):  
Hajime Fukui ◽  
Takahiro Miyazaki ◽  
Hiroyuki Ishikawa ◽  
Hiroyuki Nakajima ◽  
Naoki Mochizuki

AbstractCardiac precursor cells (CPCs) in the first heart field (FHF) and the second heart field (SHF) present at both arterial and venous poles assemble to form a cardiac tube in zebrafish. Hippo kinase cascade is essential for proper heart formation; however, it remains elusive how Hippo signal contributes to early cardiac fate determination. We here demonstrate that mutants of large tumor suppressor kinase 1/2 (lats1/2) exhibited an increase in a SHF marker, Islet1 (Isl1)-positive and hand2 promoter-activated venous pole atrial cardiomyocytes (CMs) and that those showed expansion of the domain between between the anterior and the posterior lateral plate mesoderm. Consistently, TEAD-8 dependent transcription was activated in caudal region of the left ALPM cells that gave rise to the venous pole atrial CMs. Yap1/Wwtr1-promoted bmp2b expression was essential for Smad-regulated hand2 expression in the left ALPM, indicating that Hippo signaling restricts the SHF cells originating from the left ALPM that move toward the venous pole.


2008 ◽  
Vol 321 (1) ◽  
pp. 150-161 ◽  
Author(s):  
Susanne Gessert ◽  
Daniel Maurus ◽  
Thomas Brade ◽  
Paul Walther ◽  
Petra Pandur ◽  
...  

2007 ◽  
Vol 290 (1) ◽  
pp. 115-122 ◽  
Author(s):  
Adriana C. Gittenberger-De Groot ◽  
Edris A.F. Mahtab ◽  
Nathan D. Hahurij ◽  
Lambertus J. Wisse ◽  
Marco C. Deruiter ◽  
...  

2013 ◽  
Vol 113 (4) ◽  
pp. 350-351 ◽  
Author(s):  
Sean M. Stevens ◽  
William T. Pu

2021 ◽  
Vol 8 (4) ◽  
pp. 41
Author(s):  
Catherine Pfefferli ◽  
Hannah R. Moran ◽  
Anastasia Felker ◽  
Christian Mosimann ◽  
Anna Jaźwińska

The vertebrate heart integrates cells from the early-differentiating first heart field (FHF) and the later-differentiating second heart field (SHF), both emerging from the lateral plate mesoderm. In mammals, this process forms the basis for the development of the left and right ventricle chambers and subsequent chamber septation. The single ventricle-forming zebrafish heart also integrates FHF and SHF lineages during embryogenesis, yet the contributions of these two myocardial lineages to the adult zebrafish heart remain incompletely understood. Here, we characterize the myocardial labeling of FHF descendants in both the developing and adult zebrafish ventricle. Expanding previous findings, late gastrulation-stage labeling using drl-driven CreERT2 recombinase with a myocardium-specific, myl7-controlled, loxP reporter results in the predominant labeling of FHF-derived outer curvature and the right side of the embryonic ventricle. Raised to adulthood, such lineage-labeled hearts retain broad areas of FHF cardiomyocytes in a region of the ventricle that is positioned at the opposite side to the atrium and encompasses the apex. Our data add to the increasing evidence for a persisting cell-based compartmentalization of the adult zebrafish ventricle even in the absence of any physical boundary.


2013 ◽  
Vol 15 (9) ◽  
pp. 1098-1106 ◽  
Author(s):  
Daniela Später ◽  
Monika K. Abramczuk ◽  
Kristina Buac ◽  
Lior Zangi ◽  
Maxine W. Stachel ◽  
...  

2021 ◽  
Author(s):  
Catherine Pfefferli ◽  
Hannah R. Moran ◽  
Anastasia Felker ◽  
Christian Mosimann ◽  
Anna Jazwinska

The vertebrate heart integrates cells from the early-differentiating first heart field (FHF) and the later-differentiating second heart field (SHF) emerging from the lateral plate mesoderm. In mammals, this process forms the basis for the development of the left and right ventricle chambers and subsequent chamber septation. The single ventricle-forming zebrafish heart also integrates FHF and SHF lineages during embryogenesis, yet the contributions of these two myocardial lineages to the adult zebrafish heart remain incompletely understood. Here, we characterize the myocardial labeling of FHF descendants in both the developing and adult zebrafish ventricle. Expanding previous findings, late gastrulation-stage labeling using drl-driven CreERT2 recombinase with a myocardium-specific, myl7-controlled loxP reporter results in predominant labeling of FHF-derived outer curvature and the right side of the embryonic ventricle. Raised to adulthood, such lineage-labeled hearts retain broad areas of FHF cardiomyocytes in a region of the ventricle that is positioned at the opposite side to the atrium and encompasses the apex. Our data add to the increasing evidence for a persisting cell-based compartmentalization of the adult zebrafish ventricle even in the absence of any physical boundary.


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