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Biology of Reproduction, Vol 11, 85-92, Copyright © 1974 by Society for the Study of Reproduction
1 Department of Anatomy, University of Turku, SF-20520 Turku 52, Finland The stages of the seminiferous epithelial cycle are recognizable in freshly isolated
rat seminiferous tubules by a simple transillumination technique. By phase contrast microscopy on cells squeezed out from an isolated piece of tubule, the developmental stage
of live germinal cells can be accurately determined. The kinetics of some organelles
in early postmeiotic spermatids were followed by means of videotape recording and time-lapse cinemicrography. Pieces of tubules containing cells of corresponding developmental
stages were prepared for electron microscopy. Immediately after the second meiotic division the chromatoid body and the Golgi
apparatus are dispersed in the cytoplasm of the young spermatid as small dark bodies.
But very soon, during stage 1 of spermiogenesis, these organelles assume the compacted
form typical of the next stages. This morphogenesis involves the presence of vesicles
of continuously and rather rapidly changing configuration. During stage 2, the chromatoid body rapidly moves on the nuclear envelope. It continuously sends and receives small dark particles and light vesicles and produces transient
shallow depressions or occasionally deep indentations in the nuclear envelope. During
its movements the chromatoid body also makes transient contacts with the Golgi apparatus.
At stage 3 these movements slow down and practically cease at the stage 5. The rapid nonrandom movements of the chromatoid body and associated granules
and vesicles suggest that this organelle participates from the early stages of spermiogenesis
in spermatid maturation. The early activities of the chromatoid body, especially at stage
I, may be heat labile.
2 Department of Electron Microscopy, University of Turku, SF-20520 Turku 52, Finland
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