Stimulation of brain development in chick embryo by elevated temperatureZamenhof, Stephen
doi: 10.1007/BF00848881pmid: 28304892
Experimental chick embryos were incubated at 37.5°C till day 7 and after day 10, and at 40.5°C on days 7–10; their optic lobes and cerebral hemispheres at day 10 and at hatching were compared with controls incubated at 37.5°C only. Cell numbers at day 10 were directly counted by a new method involving formalin fixation and cell disaggregation by gentle sonication. At hatching, body weights, organ weights and organ DNA (cell numbers) were the same in experimentals and in controls, for both optic lobes and cerebral hemispheres, though the protein contents were significantly higher in experimentals. However, at 10 days (end of neuron proliferation) the weights and the cell numbers in experimentals were significantly higher. Two possible explanations have been offered: 1. Elevated neuron population in experimental animals at day 10 is followed by their elevated death rate, or 2. The increment in neuron number is permanent but at hatching it is overshadowed by the population of other cells.
Gynandromorph analysis of the thoracic disc primordia inDrosophila melanogasterWieschaus, Eric; Gehring, Walter
doi: 10.1007/BF00848883pmid: 28304894
Cell lineage relationships observable inDrosophila gynandromorphs have been used to locate the primordia of the individual thoracic disc relative to each other in the embryo. Three observations indicate that the borders of the individual disc primordia lie very close to each other, separated by few if any non-disc cells.First, the frequency of mosaicism within each disc indicates large primordia, of similar magnitude to the distances between the centres of adjacent primordia.Second, very few XX/XO-borders cut between adjacent discs without also cutting into one or the other disc.Third, sturt distances between points on adjacent discs are often much smaller than distances measured within individual discs. The proximity of disc primordia suggests that the individual discs might share common precursor cells in the early embryo.
Regeneration and endocrinology in the polychaetePlatynereis dumeriliiHofmann, D.
doi: 10.1007/BF00848884pmid: 28304895
1.
In the polychaetePlatynereis dumerilii, the hormone-elaborating portion of the prostomium was determined by means of prostomium transection and implantation experiments. The area in question lies between the two pairs of eyes, extending longitudinally from the posterior border of the anterior eyes to about the posterior border of the posterior eyes. This corresponds approximately with the brain area delimited by the anterior and posterior dorsoventral connective tissue tubes and which is covered ventrally by the infracerebral gland epithelium.
2.
The infracerebral gland-complex and neurosecretory neurons within the brain were envisaged as possible sites of hormone synthesis.
3.
The infracerebral gland-complex inPl. dumerilii was investigated with light—and electron-microscopical techniques. A leaf-shaped area (measuring 120 by 95 μm at the most) of the pericapsular epithelium at the ventral side of the brain, adjacent to the main blood vessel and to its efferent branches, consists of specialized columnar epithelial cells. Numerousa-cells and scarceb-cells can be distinguished. Fibre tracts with glia fibres and axons (some being neurosecretory axons) descend from the neuropile and in part terminate with prominent end-structures at the inner face of the brain capsule in the gland region. Probably some axons penetrate the capsule and make contact with the gland cells. Neither structural nor experimental findings prove that the infracerebral gland synthesizes the brain hormone. Accessory functions are discussed.
4.
Investigations in secretory brain cells ofPl. dumerilii are reported. In agreement with Müller (1973), a lack of correlation between the number of stainable neurosecretory neurons and the hormonal activity of the brain was found: in immature worms (to which high hormonal titers are ascribed) only few or even no neurosecretory brain cells at all were detectable. Prostomium transection and implantation experiments show further that not all regions of the brain which enclose neurosecretory neurons produce brain hormone. The results are discussed with reference to the hypotheses of Müller (1973) which suggest that the appearance of stainable neurosecretory brain cells indicates inactivation of neurons possibly previously involved with hormone synthesis.