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Biology of Reproduction, Vol 19, 712-719, Copyright © 1978 by Society for the Study of Reproduction
1 Department of Animal Physiology,
Institute of Zoology,
Jagiellonian University,
Krakow, Poland
and
Department of Animal Science,
Animal Genetics Laboratory,
University of Illinois,
Urbana, Illinois 6180l Theca interna cells were collected from large porcine follicles in the follicular phase of the
cycle. The theca interna layer was manually separated from the theca externa, washed thoroughly,
occasionally treated with hyaluronidase solution and trypsinized. The resulting cell suspension
consisted of approximately 70% theca interna cells, 8% granulosa cells and 23% nonsteroidogenic
cells. In one experiment, cells collected from the granulosa layer and the theca interna of the same
follicles were compared. Specific cell types were identified by: 1) staining with Oil Red O (ORO)
to visualize lipid droplets in the cytoplasm; 2) measuring activity of the Theca interna cells can be distinguished from granulosa cells in suspension prior to culture by
the following criteria: 1) more intense staining with ORO; 2) stronger
5, 3
-hydroxysteroid
dehydrogenase (
5, 3
-OH SH) enzyme and 3) quantitating estrogen production by the cultured
cells. Nonsteroidogenic cells do not stain by any of the techniques applied.
5, 3
-OH SH activity and
3) larger cell size. Theca interna cells in culture can be differentiated from granulosa cells by the
following parameters: 1) more elongated shape; 2) slower and more chaotic growth; 3) weaker
enzyme activity and 4) increased estrogen production.
Note:
ACKNOWLEDGEMENTS
We are greatly indebted to Professor A. V. Nalbandov for his constant interest, support and correction
of the manuscript; to Dr. C. Channing for valuable
suggestions and to Dr. B. Grygon, Mrs. Alberta McClara and Mrs. Jane Harris for their technical and
clerical assistance.
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