Retinoic acid causes the development of feathers in the scale-forming integument of the chick embryo

1978 ◽  
Vol 185 (2) ◽  
pp. 195-200 ◽  
Author(s):  
Danielle Dhouailly ◽  
Margaret Hurlstone Hardy
Keyword(s):  
Retinoic Acid ◽  
Chick Embryo

scholarly journals Cellular uptake of retinoic acid in vitro

1980 ◽  
Vol 190 (3) ◽  
pp. 839-842 ◽  
Author(s):  
C K Banerjee ◽  
B P Sani
Keyword(s):  
Retinoic Acid ◽  
Chick Embryo ◽  
Acid Concentration ◽  
Cellular Uptake ◽  
Protein Complex ◽  
Incubation Medium ◽  
Temperature Dependent ◽  
Colon Tumour ◽  
Mouse Colon

Incubation of chick embryo skin and mouse colon tumour 26 with [3H]retinoic acid resulted in the formation of a complex of retinoic acid and its cellular binding protein both in cytosol and in nuclei. Formation of the ligand—protein complex was temperature-dependent and increased with increases in retinoic acid concentration in the incubation medium. About 3—8% of the ligand present in the cytosol was associated with the nuclei.

scholarly journals Interactions between FGF18 and retinoic acid regulate differentiation of chick embryo limb myoblasts

2014 ◽  
Vol 396 (2) ◽  
pp. 214-223 ◽  
Author(s):  
Gi Fay Mok ◽  
Ryan Cardenas ◽  
Helen Anderton ◽  
Keith H.S. Campbell ◽  
Dylan Sweetman
Keyword(s):  
Retinoic Acid ◽  
Chick Embryo

The role of retinoid-binding proteins in the generation of pattern in the developing limb, the regenerating limb and the nervous system

Development ◽  
1989 ◽  
Vol 107 (Supplement) ◽  
pp. 109-119 ◽  
Author(s):  
M. Maden ◽  
D. E. Ong ◽  
D. Summerbell ◽  
F. Chytil
Keyword(s):  
Nervous System ◽  
Retinoic Acid ◽  
Chick Embryo ◽  
Neural Tube ◽  
Floor Plate ◽  
Limb Bud ◽  
Commissural Axons ◽  
New Information ◽  
Mantle Layer ◽  
Developing Nervous System

We summarise existing data and describe new information on the levels and distribution of cellular retinoic acid-binding protein (CRABP) and cellular retinolbinding protein (CRBP) in the regenerating axolotl limb, the developing chick limb bud and the nervous system of the chick embryo in the light of the known morphogenetic effects of retinoids on these systems. In the regenerating limb, levels of CRABP rise 3- to 4-fold during regeneration, peaking at the time when retinoic acid (RA) is most effective at causing pattern duplications. The levels of CRBP are low. The potency of various retinoids in causing pattern respecification correlates well with the ability of these compounds to bind to CRABP. In the chick limb bud, the levels of CRABP are high and the levels of CRBP are low. Again the binding of various retinoids to CRABP correlates well with their ability to cause pattern duplications. By immunocytochemistry, we show that CRABP is present at high levels in the progress zone of the limb bud and is distributed across the anteroposterior axis in a gradient with the high point at the anterior margin. In the chick embryo, CRABP levels are high and CRBP levels are low. By immunocytochemistry, CRABP is localised primarily to the developing nervous system, labelling cells and axons in the mantle layer of the neural tube. These become the neurons of the commissural system. Also sensory axons label intensely with CRABP whereas motor axons do not and in the mixed nerves at the brachial plexus sensory and motor components can be distinguished on this basis. In the neural tube, CRBP only stains the ventral floor plate. Since the ventral floor plate may be a source of chemoattractant for commissural axons, we suggest on the basis of these staining patterns that RA may fulfill this role and thus be involved morphogenetically in the developing nervous system.

An early marker of axial pattern in the chick embryo and its respecification by retinoic acid

Development ◽  
1992 ◽  
Vol 114 (4) ◽  
pp. 841-852 ◽  
Author(s):  
O. Sundin ◽  
G. Eichele
Keyword(s):  
Retinoic Acid ◽  
Chick Embryo ◽  
Protein A ◽  
Ectopic Expression ◽  
Primitive Streak ◽  
Expression Domain ◽  
Lateral Plate ◽  
Antibody Staining ◽  
Discrete Band ◽  
Stage Embryo

Chick Ghox 2.9 protein, a homeodomain-containing polypeptide, is first detected in the mid-gastrula stage embryo and its levels increase rapidly in the late gastrula. At this time, the initially narrow band of expression along the primitive streak expands laterally to form a shield-like domain that encompasses almost the entire posterior region of the embryo and extends anteriorly as far as Hensen's node. We have found that this expression domain co-localizes with a morphological feature that consists of a stratum of refractile, thickened mesoderm. Antibody-staining indicates that Ghox 2.9 protein is present in all cells of this mesodermal region. In contrast, expression within the ectoderm overlying the region of refractile mesoderm varies considerably. The highest levels of expression are found in ectoderm near the streak and surrounding Hensen's node, regions that recent fate mapping studies suggest that primarily destined to give rise to neurectoderm. At the definitive streak stage (Hamburger and Hamilton stage 4) the chick embryo is especially sensitive to the induction of axial malformations by retinoic acid. Four hours after the treatment of definitive streak embryos with a pulse of retinoic acid the expression of Ghox 2.9 protein is greatly elevated. This ectopic expression occurs in tissues anterior to Hensen's node, including floor plate, notochord, presumptive neural plate and lateral plate mesoderm, but does not occur in the anteriormost region of the embryo. The ectopic induction of Ghox 2.9 is strongest in ectoderm, and weaker in the underlying mesoderm. Endoderm throughout the embryo is unresponsive. At stage 11, Ghox 2.9 is normally expressed at high levels within rhombomere 4 of the developing hindbrain. In retinoic-acid-treated embryos which have developed to this stage, typical rhombomere boundaries are largely absent. Nevertheless, Ghox 2.9 is still expressed as a discrete band, but one that is widened and displaced to a more anterior position.

Plasminogen activator in chick embryo muscle cells: Induction of enzyme by RSV, PMA and retinoic acid

Cell ◽  
1978 ◽  
Vol 15 (4) ◽  
pp. 1301-1312 ◽  
Author(s):  
Ruth Miskin ◽  
Thomas G. Easton ◽  
E. Reich
Keyword(s):  
Retinoic Acid ◽  
Chick Embryo ◽  
Plasminogen Activator ◽  
Muscle Cells

scholarly journals New aspects of the control of retinoic acid synthesis in the chick embryo

2009 ◽  
Vol 331 (2) ◽  
pp. 398 ◽  
Author(s):  
Malcolm Maden ◽  
Susan Reijntjes
Keyword(s):  
Retinoic Acid ◽  
Chick Embryo ◽  
Acid Synthesis

scholarly journals The uptake and metabolism of retinol, retinoic acid and methyl retinoate by the early chick embryo

1969 ◽  
Vol 23 (4) ◽  
pp. 899-904 ◽  
Author(s):  
B. Morgan ◽  
J. N. Thompson ◽  
G. A. J. Pitt
Keyword(s):  
Retinoic Acid ◽  
Chick Embryo ◽  
Vitamin A ◽  
Early Embryo ◽  
Radioactive Substance ◽  
Chain Fatty Acid ◽  
Long Chain Fatty Acid ◽  
Early Chick Embryo ◽  
Uptake And Metabolism ◽  
Very High

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.

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