Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1970 Sep 1;46(3):491–504. doi: 10.1083/jcb.46.3.491

METABOLIC AND ULTRASTRUCTURAL CHANGES IN THE FROG OVARIAN FOLLICLE IN RESPONSE TO PITUITARY STIMULATION

John Walberg Anderson 1, Milton B Yatvin 1
PMCID: PMC2107872  PMID: 4949847

Abstract

Frog ovarian fragments were prevented from ovulating in vitro by the addition of actinomycin D up to 3 hr following pituitary stimulation; but addition of Actinomycin D 6 hr after stimulation was far less effective. Puromycin, on the other hand, effectively inhibited ovulation when added as late as 6 hr after pituitary stimulation. Although actinomycin D reduced uptake of uridine-3H, and puromycin reduced uptake of leucine-3H and lysine-14 by pituitary-stimulated ovarian tissue minus oocytes (OTMO) in vitro, it was found that pituitary stimulation did not significantly increase uptake of these compounds by OTMO. Radioautographs of ovarian follicles fixed 6 hr after the addition of pituitary extract and uridine-3H in vitro revealed increased RNA synthesis in the peritoneal surface epithelium, compared with unstimulated controls, while the ovarian sac epithelium showed no increase. Gross ultrastructural changes occurred in the peritoneal area of ovarian follicles following pituitary stimulation in vivo, including loss of collagen fibrils, and general disorganization of the connective tissue theca. Changes in the rough endoplasmic reticulum of the peritoneal epithelial cells, while frequently encountered, were less pronounced. None of these changes was observed in the ovarian sac area, or in the interfollicular region. The above data are consistent with the hypothesis that pituitary stimulation of the frog ovary results in increased synthesis of RNA and protein by the peritoneal epithelial cells, and that the protein may be collagenase.

Full Text

The Full Text of this article is available as a PDF (1.3 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Dettlaff T. A. Action of actinomycin and puromycin upon frog oocyte maturation. J Embryol Exp Morphol. 1966 Aug;16(1):183–195. [PubMed] [Google Scholar]
  2. Eisen A. Z., Gross J. The role of epithelium and mesenchyme in the production of a collagenolytic enzyme and a hyaluronidase in the anuran tadpole. Dev Biol. 1965 Dec;12(3):408–418. doi: 10.1016/0012-1606(65)90006-0. [DOI] [PubMed] [Google Scholar]
  3. Espey L. L., Rondell P. Collagenolytic activity in the rabbit and sow Graafian follicle during ovulation. Am J Physiol. 1968 Feb;214(2):326–329. doi: 10.1152/ajplegacy.1968.214.2.326. [DOI] [PubMed] [Google Scholar]
  4. Espey L. L. Ultrastructure of the apex of the rabbit graafian follicle during the ovulatory process. Endocrinology. 1967 Aug;81(2):267–276. doi: 10.1210/endo-81-2-267. [DOI] [PubMed] [Google Scholar]
  5. HOPE J., HUMPHRIES A. A., Jr, BOURNE G. H. ULTRASTRUCTURAL STUDIES ON DEVELOPING OOCYTES OF THE SALAMANDER TRITURUS VIRIDESCENS. I. THE RELATIONSHIP BETWEEN FOLLICLE CELLS AND DEVELOPING OOCYTES. J Ultrastruct Res. 1963 Oct;59:302–324. doi: 10.1016/s0022-5320(63)80009-x. [DOI] [PubMed] [Google Scholar]
  6. Honig G. R., Rabinovitz M. Actinomycin D: inhibition of protein synthesis unrelated to effect on template RNA synthesis. Science. 1965 Sep 24;149(3691):1504–1506. doi: 10.1126/science.149.3691.1504. [DOI] [PubMed] [Google Scholar]
  7. Kessel R. G., Panje W. R. Organization and activity in the pre- and postovulatory follicle of Necturus maculosus. J Cell Biol. 1968 Oct;39(1):1–34. doi: 10.1083/jcb.39.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  9. Pool W. R., Lipner H. Inhibition of ovulation by antibiotics. Endocrinology. 1966 Nov;79(5):858–864. doi: 10.1210/endo-79-5-858. [DOI] [PubMed] [Google Scholar]
  10. REVEL M., HIATT H. H., REVEL J. P. ACTINOMYCIN D: AN EFFECT ON RAT LIVER HOMOGENATES UNRELATED TO ITS ACTION ON RNA SYNTHESIS. Science. 1964 Dec 4;146(3649):1311–1313. doi: 10.1126/science.146.3649.1311. [DOI] [PubMed] [Google Scholar]
  11. REYNOLDS E. S. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol. 1963 Apr;17:208–212. doi: 10.1083/jcb.17.1.208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. RONDELL P. A., WRIGHT P. A. Oxygen consumption in ovulating fragments of ovaries of Rana pipiens. Science. 1957 Apr 5;125(3249):644–645. doi: 10.1126/science.125.3249.644. [DOI] [PubMed] [Google Scholar]
  13. Roberts A. N., Hunt J. S. A modified Dominici technic for autoradiography: acidified eosin-orange and alcoholic toluidine blue. Stain Technol. 1967 Jan;42(1):7–10. doi: 10.3109/10520296709114974. [DOI] [PubMed] [Google Scholar]
  14. Usuku G., Gross J. Morphologic studies of connective tissue resorption in the tail fin of metamorphosing bullfrog tadpole. Dev Biol. 1965 Jun;11(3):352–370. doi: 10.1016/0012-1606(65)90044-8. [DOI] [PubMed] [Google Scholar]
  15. Wannemacher R. W., Jr, Banks W. L., Jr, Wunner W. H. Use of a single tissue extract to determine cellular protein and nucleic acid concentrations and rate of amino acid incorporation. Anal Biochem. 1965 May;11(2):320–326. doi: 10.1016/0003-2697(65)90020-5. [DOI] [PubMed] [Google Scholar]
  16. Wischnitzer S. The ultrastructure of the cytoplasm of the developing amphibian egg. Adv Morphog. 1966;5:131–179. doi: 10.1016/b978-1-4831-9952-8.50008-0. [DOI] [PubMed] [Google Scholar]
  17. ZACHARIAE F., JENSEN C. E. Studies on the mechanism of ovulation: histochemical and physico-chemical investigations on genuine follicular fluids. Acta Endocrinol (Copenh) 1958 Mar;27(3):343–355. [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES