AI Article Synopsis
- A method for obtaining embryo brain slices is detailed, focusing on rhombencephalon and mesencephalon cultivation using a technique called the "swimming float."
- The cultivation maintains the original brain structure relationships, enabling accurate comparison with histological sections.
- Key findings include newly described cultured neurons and differences in development compared to in vivo conditions, suggesting lack of external stimulation affects neuron morphology.
Article Abstract
A method and device for obtaining embryo brain slices are described. Results of cultivation of slices of rhombencephalon and mesencephalon are presented obtained in accord with a proposed technique of the "swimming float" (Olenev, 1979). With this cultivation, original topographical relations between brain nuclei and fibrillar tracts remain unchanged that enables us to compare these cultures with histological sections of brain to identify strictly the structures being cultivated. Cultured neurons of nuclei of XII and VIII pairs of cranial nerves have been first described in addition to various divisions of the reticular formation commissura cochlearis dorsalis. Compared to cells examined in the in vivo conditions, neurons of the nucleus cochlearis laminaris, grown in tissue culture conditions, do not make plate-forming structures; dendrites of the neurons of III layer of tectum opticum do not develop. This may be explained by the absence in vitro of any stimulating influence from the acustic ganglion fibres and ganglion cells of the retina on these morphogenetic processes.
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