The effects of retinoic acid on heart formation in the early chick embryo

Development ◽  
1991 ◽  
Vol 113 (4) ◽  
pp. 1405-1417 ◽  
Author(s):  
M.K. Osmond ◽  
A.J. Butler ◽  
F.C. Voon ◽  
R. Bellairs

The vitamin A derivative retinoic acid has previously been shown to have teratogenic effects on heart development in mammalian embryos. The craniomedial migration of the precardiac mesoderm during the early stages of heart formation is thought to depend on a gradient of extracellular fibronectin associated with the underlying endoderm. Here, the effects of retinoic acid on migration of the precardiac mesoderm have been investigated in the early chick embryo. When applied to the whole embryo in culture, the retinoid inhibits the craniomedial migration of the precardiac mesoderm resulting in a heart tube that is stunted cranially, while normal or enlarged caudally. Similarly, a local application of retinoic acid to the heart-forming area disrupts the formation of the cardiogenic crescent and the subsequent development of a single mid-line heart tube. This effect is analogous to removing a segment of endoderm and mesoderm across the heart-forming area and results in various degrees of cardia bifida. At higher concentrations of retinoic acid and earlier developmental stages, two completely separate hearts are produced, while at lower concentrations and later stages there are partial bifurcations. The controls, in which the identical operation is carried out except that dimethyl sulphoxide (DMSO) is used instead of the retinoid, are almost all normal. We propose that one of the teratogenic effects of retinoic acid on the heart is to disrupt the interaction between precardiac cells and the extracellular matrix thus inhibiting their directed migration on the endodermal substratum.

1969 ◽  
Vol 23 (4) ◽  
pp. 899-904 ◽  
Author(s):  
B. Morgan ◽  
J. N. Thompson ◽  
G. A. J. Pitt

1. Fertile eggs deficient in vitamin A were obtained by feeding hens a diet deficient in retinol (vitamin A alcohol) but containing methyl retinoate.2. Radioactive retinol was injected into the albumen of three of these eggs at a level of 2 μg [6,7-14C]retinol/egg. After 5 days' incubation, 4.6–8.3% of the injected material was recovered in the lipid of the embryo, representing a four- to nine-fold concentration into the embryo from the albumen. Approximately 40–50% of this was unchanged retinol, 15–20% retin-aldehyde and 20–30% probably a long-chain fatty acid retinyl ester. The early embryo can, therefore, metabolize vitamin A very effectively.3. [6,7-14C]Retinoic acid (2 μg) was injected into normal fertile eggs, killing most of the embryos. The eggs with dead embryos were analysed; 0.24% and 0.33% of the injected material was recovered from the embryos. Two embryos which developed contained 0.51% and 0.53% of the injected dose. In no instance was any material identified other than retinoic acid. The extremely low amounts of retinoic acid absorbed by the embryos emphasize the very high toxicity of retinoic acid to the early chick embryo.4. [6,7-14C]Methyl retinoate (0.5 μg) was injected into each of four normal eggs; 8.5–11.6% was isolated as unchanged methyl retinoate after 5 days; no other radioactive substance was detected.


2005 ◽  
Vol 25 (10) ◽  
pp. 4200-4210 ◽  
Author(s):  
Jianbo Wang ◽  
Ye Tao ◽  
Ingolf Reim ◽  
Kathleen Gajewski ◽  
Manfred Frasch ◽  
...  

ABSTRACT Early heart development in Drosophila and vertebrates involves the specification of cardiac precursor cells within paired progenitor fields, followed by their movement into a linear heart tube structure. The latter process requires coordinated cell interactions, migration, and differentiation as the primitive heart develops toward status as a functional organ. In the Drosophila embryo, cardioblasts emerge from bilateral dorsal mesoderm primordia, followed by alignment as rows of cells that meet at the midline and morph into a dorsal vessel. Genes that function in coordinating cardioblast organization, migration, and assembly are integral to heart development, and their encoded proteins need to be understood as to their roles in this vital morphogenetic process. Here we prove the Toll transmembrane protein is expressed in a secondary phase of heart formation, at lateral cardioblast surfaces as they align, migrate to the midline, and form the linear tube. The Toll dorsal vessel enhancer has been characterized, with its activity controlled by Dorsocross and Tinman transcription factors. Consistent with the observed protein expression pattern, phenotype analyses demonstrate Toll function is essential for normal dorsal vessel formation. Such findings implicate Toll as a critical cell adhesion molecule in the alignment and migration of cardioblasts during dorsal vessel morphogenesis.


1999 ◽  
Vol 216 (1) ◽  
pp. 282-296 ◽  
Author(s):  
Eric C. Swindell ◽  
Christina Thaller ◽  
Shanthini Sockanathan ◽  
Martin Petkovich ◽  
Thomas M. Jessell ◽  
...  

Nature ◽  
1965 ◽  
Vol 205 (4975) ◽  
pp. 1006-1007 ◽  
Author(s):  
J. N. THOMPSON ◽  
J. McC. HOWELL ◽  
G. A. J. PITT ◽  
CATHERINE I. HOUGHTON

2019 ◽  
Vol 26 (29) ◽  
pp. 29763-29779 ◽  
Author(s):  
Rui Wang ◽  
Da-Guang Sun ◽  
Ge Song ◽  
Chun Yi Guan ◽  
Yi Cui ◽  
...  

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