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. 1999 Nov;195(Pt 4):515–521. doi: 10.1046/j.1469-7580.1999.19540515.x

Ultrastructural features of goat oviductal secretory cells at follicular and luteal phases of the oestrous cycle

HIROYUKI ABE 1 ,, MASAKAZU ONODERA 2 , SHICHIRO SUGAWARA 3 , TAKESHI SATOH 1 , HIROYOSHI HOSHI 1
PMCID: PMC1468022  PMID: 10634690

Abstract

The aim of the present study was to investigate the ultrastructure of secretory cells in the various regions of the goat oviduct during the follicular and luteal phases of the oestrous cycle. During the follicular phase in the fimbriae, the secretory cells contained small secretory granules with electron-dense matrices. In the luteal phase, the secretory granules disappeared and cytoplasmic protrusions, extending beyond the luminal border of the ciliated cells and often containing the nucleus, were predominant. During the follicular phase in ampullary secretory cells, numerous secretory granules with moderately electron-dense matrices were present in the supranuclear cytoplasm and exocytosis of secretory granules was observed. The number of secretory granules was dramatically reduced in the ampullary secretory cells at the luteal phase. Conspicuous cytoplasmic protrusions of secretory cells were observed similar to those of the fimbrial epithelium. Isthmic cells were almost free of secretory granules and lysosome-like bodies were found both at the follicular and luteal phases. In conclusion, our ultrastructural observations of goat oviduct revealed marked cyclic changes in the ultrastructural features of secretory cells and the ultrastructural features and the numbers of secretory granules were distinctive for each particular segment.

Keywords: Fine structure, secretion, cyclic change, reproduction

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Selected References

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  1. Abe H., Numazawa C., Abe M., Onodera M., Katsumi A. Immunocytochemical localization of oviduct-specific glycoproteins in the oviductal epithelium from cows at follicular and luteal phases. Cell Tissue Res. 1993 Oct;274(1):41–47. doi: 10.1007/BF00327983. [DOI] [PubMed] [Google Scholar]
  2. Abe H., Oikawa T. Effects of estradiol and progesterone on the cytodifferentiation of epithelial cells in the oviduct of the newborn golden hamster. Anat Rec. 1993 Mar;235(3):390–398. doi: 10.1002/ar.1092350308. [DOI] [PubMed] [Google Scholar]
  3. Abe H., Oikawa T. Examination by scanning electron microscopy of oviductal epithelium of the prolific Chinese Meishan pig at follicular and luteal phases. Anat Rec. 1992 Jul;233(3):399–408. doi: 10.1002/ar.1092330307. [DOI] [PubMed] [Google Scholar]
  4. Abe H., Oikawa T. Observations by scanning electron microscopy of oviductal epithelial cells from cows at follicular and luteal phases. Anat Rec. 1993 Mar;235(3):399–410. doi: 10.1002/ar.1092350309. [DOI] [PubMed] [Google Scholar]
  5. Abe H., Onodera M., Sugawara S. Immunological detection and characterization of an estrus-associated antigen in the goat oviduct. J Exp Zool. 1995 Jun 1;272(2):134–141. doi: 10.1002/jez.1402720207. [DOI] [PubMed] [Google Scholar]
  6. Abe H., Onodera M., Sugawara S. Scanning electron microscopy of goat oviductal epithelial cells at the follicular and luteal phases of the oestrus cycle. J Anat. 1993 Oct;183(Pt 2):415–421. [PMC free article] [PubMed] [Google Scholar]
  7. Abe H., Sendai Y., Satoh T., Hoshi H. Bovine oviduct-specific glycoprotein: a potent factor for maintenance of viability and motility of bovine spermatozoa in vitro. Mol Reprod Dev. 1995 Oct;42(2):226–232. doi: 10.1002/mrd.1080420212. [DOI] [PubMed] [Google Scholar]
  8. Abe H. The mammalian oviductal epithelium: regional variations in cytological and functional aspects of the oviductal secretory cells. Histol Histopathol. 1996 Jul;11(3):743–768. [PubMed] [Google Scholar]
  9. BJORKMAN N., FREDRICSSON B. The ultrastructural organization and the alkaline phosphatase activity of the epithelial surface of the bovine fallopian tube. Z Zellforsch Mikrosk Anat. 1960;51:589–596. [PubMed] [Google Scholar]
  10. Bajpai V. K., Shipstone A. C., Gupta D. N., Karkun J. N. Differential response of the ampullary and isthmic cells to ovariectomy and estrogen treatment: an ultrastructural study. Endokrinologie. 1977 Feb;69(1):11–20. [PubMed] [Google Scholar]
  11. Fredricsson B., Holm S. Dissociated response of the epithelium of the rabbit oviduct to estrogen. Biol Reprod. 1974 Aug;11(1):40–49. doi: 10.1095/biolreprod11.1.40. [DOI] [PubMed] [Google Scholar]
  12. Gandolfi F. Functions of proteins secreted by oviduct epithelial cells. Microsc Res Tech. 1995 Sep 1;32(1):1–12. doi: 10.1002/jemt.1070320102. [DOI] [PubMed] [Google Scholar]
  13. Gandolfi F., Moor R. M. Stimulation of early embryonic development in the sheep by co-culture with oviduct epithelial cells. J Reprod Fertil. 1987 Sep;81(1):23–28. doi: 10.1530/jrf.0.0810023. [DOI] [PubMed] [Google Scholar]
  14. Hunter R. H., Fléchon B., Fléchon J. E. Distribution, morphology and epithelial interactions of bovine spermatozoa in the oviduct before and after ovulation: a scanning electron microscope study. Tissue Cell. 1991;23(5):641–656. doi: 10.1016/0040-8166(91)90020-t. [DOI] [PubMed] [Google Scholar]
  15. Hunter R. H. Modulation of gamete and embryonic microenvironments by oviduct glycoproteins. Mol Reprod Dev. 1994 Oct;39(2):176–181. doi: 10.1002/mrd.1080390209. [DOI] [PubMed] [Google Scholar]
  16. King R. S., Anderson S. H., Killian G. J. Effect of bovine oviductal estrus-associated protein on the ability of sperm to capacitate and fertilize oocytes. J Androl. 1994 Sep-Oct;15(5):468–478. [PubMed] [Google Scholar]
  17. Pollard J. W., Plante C., King W. A., Hansen P. J., Betteridge K. J., Suarez S. S. Fertilizing capacity of bovine sperm may be maintained by binding of oviductal epithelial cells. Biol Reprod. 1991 Jan;44(1):102–107. doi: 10.1095/biolreprod44.1.102. [DOI] [PubMed] [Google Scholar]
  18. Prichard J. F., Thibodeaux J. K., Pool S. H., Blakewood E. G., Menezo Y., Godke R. A. In-vitro co-culture of early stage caprine embryos with oviduct and uterine epithelial cells. Hum Reprod. 1992 Apr;7(4):553–557. doi: 10.1093/oxfordjournals.humrep.a137689. [DOI] [PubMed] [Google Scholar]
  19. Suarez S., Redfern K., Raynor P., Martin F., Phillips D. M. Attachment of boar sperm to mucosal explants of oviduct in vitro: possible role in formation of a sperm reservoir. Biol Reprod. 1991 Jun;44(6):998–1004. doi: 10.1095/biolreprod44.6.998. [DOI] [PubMed] [Google Scholar]
  20. Verhage H. G., Brenner R. M. Estradiol-induced differentiation of the oviductal epithelium in ovariectomized cats. Biol Reprod. 1975 Aug;13(1):104–111. doi: 10.1095/biolreprod13.1.104. [DOI] [PubMed] [Google Scholar]

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