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Biology of Reproduction, Vol 25, 871-883, Copyright © 1981 by Society for the Study of Reproduction
1 Department of Anatomy,
University of Virginia, School of Medicine,
Charlottesville, Virginia 22908 The synthesis, intracellular transport, and secretion of proteins were studied in different parts
of the mouse epididymis. Adult mice were administered [3H]leucine, and at subsequent intervals
between 10 min and 12 h two animals were killed. Samples of initial, middle, and terminal segments were prepared for light and electron microscope radioautography. In the initial and middle
segments, the proportion of silver grains showed successive peaks over endoplasmic reticulum,
Golgi apparatus, coated vesicles, and the apical cell surface. Labeling of luminal contents increased
at the end of this sequence, at 1-2 h after injection of precursor. These events, however, occurred
earlier in the middle segment than in the initial segment. Similar structures were labeled in the
terminal segment, but radioactivity of the rough endoplasmic reticulum remained relatively high,
peaks in labeling of other organelles were not sharp, and luminal labeling did not rise as much as in
the more proximal segments. The results suggest that the synthesis and transport of proteins was
more rapid in the middle than in the initial segment. At least in the middle segment, the sparsely
granulated reticulum appeared to participate in protein synthesis along with the rough endoplasmic
reticulum. In both initial and middle segments, coated vesicles may have been involved in transport
from the Golgi apparatus to the cell surface and lumen. Relatively little protein secretion occurred
in the terminal segment, where much newly synthesized protein appeared to be retained within the
epithelial cells. The findings are related to the function of sperm maturation in initial and middle
segments and of sperm storage in the terminal segment.
Note:
ACKNOWLEDGMENTS
The author is indebted for technical assistance to
Ms. Mary Stuart and Ms. Kathleen Glasheen. This
work was supported by grants from NSF (PCM78-22242) and NIH (HD10073).
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