2020
DOI: 10.1002/dvdy.229
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Notch and Bmp signaling pathways act coordinately during the formation of the proepicardium

Abstract: Background: The epicardium is the outer mesothelial layer of the heart. It encloses the myocardium and plays key roles in heart development and regeneration. It derives from the proepicardium (PE), cell clusters that appear in the dorsal pericardium (DP) close to the atrioventricular canal and the venous pole of the heart, and are released into the pericardial cavity. PE cells are advected around the beating heart until they attach to the myocardium. Bmp and Notch signaling influence PE formation, but it is un… Show more

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Cited by 8 publications
(4 citation statements)
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“…Utilizing zebrafish as a model and combining transgenic reporters, via CRISPR/Cas9, different studies have performed functional testing of candidate genes associated with CHD. The results obtained showed that genes encoding transcription factors, such as GATA4/5/6 [ 100 , 101 ], NKX2.5 [ 102 ], and HAND2 [ 103 , 104 ], or cell signaling molecules, such as NOTCH1 [ 105 , 106 ] and SMAD6 [ 107 , 108 ] cause CHD in humans and play an important role for heart development in zebrafish. In addition, genes associated with cardiomyocyte function, which cause CHD in zebrafish include MYH6 [ 109 ], ACTC [ 110 ], TITIN [ 111 ], and KCNH2 [ 112 ].…”
Section: Zebrafish To Study Human Cardiac and Vessel Alterationsmentioning
confidence: 99%
“…Utilizing zebrafish as a model and combining transgenic reporters, via CRISPR/Cas9, different studies have performed functional testing of candidate genes associated with CHD. The results obtained showed that genes encoding transcription factors, such as GATA4/5/6 [ 100 , 101 ], NKX2.5 [ 102 ], and HAND2 [ 103 , 104 ], or cell signaling molecules, such as NOTCH1 [ 105 , 106 ] and SMAD6 [ 107 , 108 ] cause CHD in humans and play an important role for heart development in zebrafish. In addition, genes associated with cardiomyocyte function, which cause CHD in zebrafish include MYH6 [ 109 ], ACTC [ 110 ], TITIN [ 111 ], and KCNH2 [ 112 ].…”
Section: Zebrafish To Study Human Cardiac and Vessel Alterationsmentioning
confidence: 99%
“…Furthermore, the BMP signaling promotes the development of endocardial cells (ECs) from hPSC-derived cardiovascular progenitors[ 23 ]. It is also integrated with Notch signaling for influencing the proepicardium formation, where overexpression of Notch intracellular receptor in the endothelium enhances BMP expression and increases the number of phospho-Smad1/5 + cells for enhancing the formation of the proepicardium[ 24 ].…”
Section: Signaling Pathways During Cardiogenesismentioning
confidence: 99%
“…Specification, differentiation and development of cardiac progenitors are subjected to intense paracrine regulation mediated by different growth factors, particularly bone morphogenetic proteins (Bmps), fibroblastic growth factors (Fgfs), transforming growth factors (Tfgs) and Wnt signaling [ 1 , 2 , 3 ]. Importantly, these growth factor signals also contribute to additional cardiac morphogenetic processes, such as proepicardial/epicardial development [ 4 , 5 , 6 , 7 , 8 , 9 ], endocardial cushion formation [ 10 , 11 , 12 , 13 , 14 , 15 , 16 ] and outflow tract remodeling [ 14 , 17 , 18 , 19 ]. In addition, several other signaling pathways are also required for discrete cardiovascular morphogenetic processes, such as Hippo pathway that is fundamental for cardiomyocyte proliferation and organ size determination [ 20 , 21 , 22 ], and Notch and neuregulin signaling pathways [ 23 , 24 , 25 , 26 , 27 , 28 , 29 ] that are required for ventricular morphogenesis and maturation.…”
Section: Growth Factor Signalling In Cardiac Morphogenesismentioning
confidence: 99%