EFFECT OF DEVELOPMENTAL AGE OR TIME AFTER TRANSPLANTATION ON SERTOLI-CELL NUMBER AND TESTICULAR SIZE IN INBRED FISCHER RATS

Citation
L. Johnson et al., EFFECT OF DEVELOPMENTAL AGE OR TIME AFTER TRANSPLANTATION ON SERTOLI-CELL NUMBER AND TESTICULAR SIZE IN INBRED FISCHER RATS, Biology of reproduction, 54(5), 1996, pp. 948-959
Citations number
60
Categorie Soggetti
Reproductive Biology
Journal title
ISSN journal
00063363
Volume
54
Issue
5
Year of publication
1996
Pages
948 - 959
Database
ISI
SICI code
0006-3363(1996)54:5<948:EODAOT>2.0.ZU;2-#
Abstract
The objectives were to establish the developmental age of Fischer rats at which the Sertoli cell number is stabilized, to establish the norm al reference plateau number of Sertoli cells for evaluation of testes after transplantation, and to determine whether the developmental patt ern establishing Sertoli cell proliferation and stability are similar between intact and transplanted testes. Sertoli cell number was determ ined at ages 10-120 days in intact rats and at various times (10-90 da ys) after transplantation of prenatal or neonatal testes. Testes were fixed by vascular pefusion or by immersion with 2% glutaraldehyde and immersion in 1% osmium and were embedded in Epon 812, Sections and ser ial sections were cut at 0.5 mu m to determine the Sertoli cell nuclei volume density and the volume of an individual Sertoli cell nucleus b y brightfield microscopy or at 20 mu m to determine the maximum height and width of nuclei. A correction factor was calculated for intact (0 .663 +/- 0.025) or for transplanted 10.558 +/- 0.0291 testes to determ ine the volume of a single Sertoli cell nucleus from height and width measurements. In intact testes, Sertoli cell numbers significantly inc reased to Day 20 but were not different between 15 and 90 days. Sertol i cell number in prenatal or neonatal transplanted testes increased to 20 or 30 days posttransplantation and then stabilized to Day 60 or 90 . There was no difference in the plateau number of Sertoli cells per r at between prenatal and neonatal testes. Sertoli cells in 10-day- and 30-day-transplanted testes incorporated H-3-thymidine when placed in c ulture. A few tubules had complete spermatogenesis at 90 days posttran splantation, indicating that Sertoli cells in some of these tubules we re functional. Leydig cell structure appeared to be normal. Leukocytic infiltration of testes was not observed in intact rats or in rats rec eiving neonatal testes. Although transplanted testes showed a delay in reaching the plateau value for Sertoli cell number per testis and alt hough the value reached was lower, the developmental pattern of Sertol i cell proliferation in transplanted testes was similar to that in int act rats.