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
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.