TY - JOUR
T1 - Prostatic ductal system in rats
T2 - Regional variation in morphological and functional activities
AU - Lee, C.
AU - Sensibar, J. A.
AU - Dudek, S. M.
AU - Hiipakka, R. A.
AU - Shutsung Liao, Liao
PY - 1990
Y1 - 1990
N2 - The rat prostate is a complex ductal system with branches and subbranches extending from one end to another. Owing to the relative distance of various regions of the duct from the urethra, the entire length of the ductal system can be arbitrarily divided into three segments, i.e., the proximal, intermediate, and distal segments. The present study was carried out to assess the regional variation in cellular activities in this ductal system. Ventral prostates from adult Sprague-Dawley rats were dissected so that an individual ductal system was mechanically isolated and longitudinally sectioned to reveal various segments. Epithelial cells lining distal segments were tall-columnar type and were actively engaging in mitotic activity. Cells in intermediate segments were also tall-columnar type. However, they were mitotically quiescent, but able to produce secretory proteins. Evidence of programmed cell death was not observed in either of these two segments. Cells in proximal segments, on the other hand, were low-columnar or cuboidal in shape and were stained heavily for cathepsin D, a marker associated with late manifestation of cell death. Following castration in adult rats, there was a reversal in the site of programmed death in cells lining the ductal system. By Day 4 post-castration, distal segments contained many epithelial cells with intense cytoplasmic staining for cathepsin D while proximal segments showed a reduction in number of positively stained cells. By Day 7 post-castration, cells in proximal segments, though atrophied, were devoid of staining for cathepsin D. Therefore, there was a shift in the location of cell death from proximal segments toward distal segments in the rat prostate during castration-induced regression. These unusual phenomena of the rat prostate probably can be attributed to regional variations in responsiveness of epithelial cells to androgen stimulation and androgen depletion along the prostatic ductal system.
AB - The rat prostate is a complex ductal system with branches and subbranches extending from one end to another. Owing to the relative distance of various regions of the duct from the urethra, the entire length of the ductal system can be arbitrarily divided into three segments, i.e., the proximal, intermediate, and distal segments. The present study was carried out to assess the regional variation in cellular activities in this ductal system. Ventral prostates from adult Sprague-Dawley rats were dissected so that an individual ductal system was mechanically isolated and longitudinally sectioned to reveal various segments. Epithelial cells lining distal segments were tall-columnar type and were actively engaging in mitotic activity. Cells in intermediate segments were also tall-columnar type. However, they were mitotically quiescent, but able to produce secretory proteins. Evidence of programmed cell death was not observed in either of these two segments. Cells in proximal segments, on the other hand, were low-columnar or cuboidal in shape and were stained heavily for cathepsin D, a marker associated with late manifestation of cell death. Following castration in adult rats, there was a reversal in the site of programmed death in cells lining the ductal system. By Day 4 post-castration, distal segments contained many epithelial cells with intense cytoplasmic staining for cathepsin D while proximal segments showed a reduction in number of positively stained cells. By Day 7 post-castration, cells in proximal segments, though atrophied, were devoid of staining for cathepsin D. Therefore, there was a shift in the location of cell death from proximal segments toward distal segments in the rat prostate during castration-induced regression. These unusual phenomena of the rat prostate probably can be attributed to regional variations in responsiveness of epithelial cells to androgen stimulation and androgen depletion along the prostatic ductal system.
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U2 - 10.1095/biolreprod43.6.1079
DO - 10.1095/biolreprod43.6.1079
M3 - Article
C2 - 2291926
AN - SCOPUS:0025646614
SN - 0006-3363
VL - 43
SP - 1079
EP - 1086
JO - Biology of reproduction
JF - Biology of reproduction
IS - 6
ER -