Inhibition of nuclear migration in the absence of microtubules in the chick embryo

Development ◽  
1973 ◽  
Vol 30 (3) ◽  
pp. 661-671
Author(s):  
Paul-Emil Messier ◽  
C. Auclair

Interkinetic nuclear migration was studied in cells of the forming neural tube of cultured chick embryos aged from 1 to 7 pairs of somites. In specimens that were first exposed to 2°C for 3 h, then treated with 4 × 10−3 M monoiodoacetamide and finally transferred to new media to be reincubated for 1−2·5 h, it was found that microtubules were absent and nuclear movements blocked. These findings point to microtubules as essential structures for interkinetic nuclear migration. Their relation to the problem of neurulation is discussed.

Development ◽  
1975 ◽  
Vol 34 (2) ◽  
pp. 339-354
Author(s):  
Par Paul-Emil Messier ◽  
C. Auclair

Neurulation and interkinetic nuclear migration in the chick embryo Neurulation and interkinetic nuclear migration were studied in cells of the forming neural tube of chick embryos submitted to a variety of treatments. Our results show that cytochalasin B (5 μ/ml) does not protect microtubules against disruption occurring after 3h at 2°C nor does it prevent their repolymerization once they are cold-disrupted. However, db-cAMP protects microtubules against such cold disruption. We indicate that the inhibitory effect of cytochalasin B on interkinetic nuclear migration cannot be ascribed to an effect on microtubules.


Development ◽  
1976 ◽  
Vol 35 (1) ◽  
pp. 197-212
Author(s):  
Paul-Emil Messier

Young chick embryos were incubated on media containing formamide at concentrations of 0·1, 0·25, 0·31, 0·37, 0·43 and 0·5 M. In the neuroepithelium of these embryos we found that (1) the 0·1 M concentration had no detectable effect, (2) the 0·25 M concentration only affected mitosis which was blocked in metaphase so that mitotic figures accumulated near the neurocoele, (3) 0·31 M formamide totally inhibited interkinetic nuclear migration and affected only slightly the cell asymmetry, (4) the 0·37 M concentration considerably reduced the amount of cytoplasmic microtubules and that the cells became round, (5) at 0·43 M formamide, all microtubules had disappeared and all cells were spherical, (6) at 0·5 M formamide all cells were spherical, detached from one another and the epithelium had lost its usual characteristics. Our results on exposure of the cells to low temperature (2 °C) suggest that formamide directly affects microtubules. All the effects observed at concentrations up to 0·43 M formamide are reversible.


2015 ◽  
Vol 26 (5) ◽  
pp. 978-992 ◽  
Author(s):  
Guang Wang ◽  
Yan Li ◽  
Xiao-Yu Wang ◽  
Manli Chuai ◽  
John Yeuk-Hon Chan ◽  
...  

This is the first study of the role of BRE in embryonic development using early chick embryos. BRE is expressed in the developing neural tube, neural crest cells, and somites. BRE thus plays an important role in regulating neurogenesis and indirectly somitogenesis during early chick embryo development.


Development ◽  
1960 ◽  
Vol 8 (2) ◽  
pp. 69-72
Author(s):  
Harry Bergquist

The present paper is intended as a continuation of preceding publications (Bergquist, 1959 a, b) on possible causes of the phenomenon of ‘overgrowth’ (Patten, 1952) in the brain of the chick embryo. Reference should be made to these publications for the relevant literature. In these earlier investigations, it was observed that the mitotic rate in the altered portions of the neural tube seemed higher than in the normal regions, and that the hemispheres and tectum opticum showed marked folding. The first aim of the present investigation was to compare the volumes of the hemispheres in normal chick embryos and in corresponding stages of embryos with overgrowth, the study being confined to the distinctly evaginated portions of both hemispheres. The embryos measured consisted of those used in the previous work. The surface areas of sections through the walls of both hemispheres were determined planimetrically.


1991 ◽  
Vol 22 (7) ◽  
pp. 742-754 ◽  
Author(s):  
Sarah Guthrie ◽  
Matthew Butcher ◽  
Andrew Lumsden

Sign in / Sign up

Export Citation Format

Share Document