Hostname: page-component-586b7cd67f-t7czq Total loading time: 0 Render date: 2024-11-24T11:57:15.370Z Has data issue: false hasContentIssue false

Fine structural observations on oocyte development in monogeneans

Published online by Cambridge University Press:  06 April 2009

D. W. Halton
Affiliation:
Department of Zoology, The Queen's University, Belfast BT7 1NN, Northern Ireland
S. D. Stranock
Affiliation:
Department of Zoology, The Queen's University, Belfast BT7 1NN, Northern Ireland
Anne Hardcastle
Affiliation:
Department of Zoology, The Queen's University, Belfast BT7 1NN, Northern Ireland

Summary

The ultrastructural changes accompanying oocyte differentiation in the ovaries of the monogeneans, Diclidophora merlangi, Diplozoon paradoxum and Calicotyle kröyeri have been described. In each case, oogenesis in the ovary proceeds as far as meiotic prophase in the primary oocyte. A three-stage sequence of development based on oocyte morphology is proposed: (1) Oogonia and early, immature primary oocytes are typically undifferentiated, with chromatin-laden nuclei occupying most of the cell volume. The cytoplasm contains small clumps of mitochrondria and unattached ribosomal aggregates. There is evidence of mitosis and, in later stages, meiotic prophase is indicated by the appearance of nuclear synaptonemal complexes. (2) Maturing primary oocytes are characterized by increased nucleolar volume associated with the production of RNA for export to the cytoplasm. An organized GER and Golgi apparatus are established and involved in the synthesis and packaging of membrane-limited cortical granules. Annulate lamellae and nucleolus-like bodies appear in the cytoplasm and, with development, the cells increase in size and, peripherally, become interdigitated. (3) Mature primary oocytes represent a resting phase when cellular activity is minimal. Golgi disappear and the ER fragments or becomes reduced in dimensions. Mitochondria and free ribo-somes are numerous and cortical granules move to the cell periphery. The cells separate and, when mature, are released from the ovary. There are minor species differences in oocyte ultrastructure and development.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1976

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Anderson, E. (1968). Oocyte differentiation in the sea urchin, Arbacia punctulata, with particular reference to the origin of the cortical granules and their participation in the cortical reaction. Journal of Cell Biology 37, 514–39.CrossRefGoogle Scholar
Boyer, B. A. (1972). Ultrastructural studies of differentiation in the oocyte of the polyclad turbellarian, Prostheceraeus floridanus. Journal of Morphology 136, 273–96.CrossRefGoogle ScholarPubMed
Burton, P. R. (1960). Gametogenesis and fertilization in the frog lung fluke, Haematoloechtus medioplexus Stafford (Trematoda: Plagiorchiidae). Journal of Morphology 107, 93122.CrossRefGoogle ScholarPubMed
Burton, P. R. (1967). Fine structure of the reproductive system of a frog lung fluke. II. Penetration of the ovum by a spermatozoon. Journal of Parasitology 53, 994–9.CrossRefGoogle ScholarPubMed
Bychowsky, B. E.(1957).Monogenetic Trematodes, their Classification and Phylogeny. Moscow: Leningrad, Academy of Sciences, U.S.S.R.Google Scholar
Clérot, J.-C. (1968). Mise en évidence par cytochimie ultrastructurale de l'émission de protéines par le noyau d'auxocytes de Batraciens. Journal de Microscopie 7, 973–92.Google Scholar
Eddy, E. M. & Ito, S. (1971). Fine structural and radioautographic observations on dense perinuclear cytoplasmic material in tadpole oocytes. Journal of Cell Biology 49, 90108.CrossRefGoogle ScholarPubMed
Erasmus, D. A. (1973). A comparative study of the reproductive system of mature, immature and ‘unisexual’ female Schistosoma mansoni. Parasitology 67, 165–83.CrossRefGoogle ScholarPubMed
Gresson, R. A. R. (1964). Oogenesis in the hermaphroditic Digenea (Trematoda). Parasitology 54, 409–21.CrossRefGoogle Scholar
Hsu, W. S. (1963). The nuclear envelope in the developing oocytes in the tunicate Baltenia villosa. Zeitschrift für Zellforschung und mikroskopische Anatomie 58, 660–8.CrossRefGoogle ScholarPubMed
Kessel, R. G. (1966). An electron microscope study of nuclear cytoplasmic exchange in oocytes Ciona intestinalis. Journal of Ultrastructure Research 15, 181–96.CrossRefGoogle ScholarPubMed
Kessel, R. G. (1968 a). An electron microscope study of differentiation and growth in oocytes of Ophioderma panamensis. Journal of Ultrastructure Research 22, 6389.CrossRefGoogle ScholarPubMed
Kessel, R. G. (1968 b). Annulate lamellae. Journal of Ultrastructure Research, Supplement 10, 182.Google ScholarPubMed
Kessel, R. G. & Beams, H. W. (1968). Intranuclear membranes and nuclear-cytoplasmic exchange in young crayfish oocytes. Journal of Cell Biology 39, 735–40.CrossRefGoogle Scholar
Koulish, S. (1965). Ultrastructure of differentiating oocytes in the trematode Corgoderina attenuata. The ‘nucleolus-like’ cytoplasmic body and some lamellar membrane systems. Developmental Biology 12, 248–68.CrossRefGoogle ScholarPubMed
Koulish, S. & Kleinfield, R. (1954). The cytochemistry of an inclusion body in the oocyte of Gorgoderina attenuata, a digenetic trematode. Journal of Histochemistry and Cytochemistry 2, 481.Google Scholar
Lumsden, R. D. (1965). Macromolecular structure of glycogen in some cyclophyllidean and trypanorhynch cestodes. Journal of Parasitology 51, 501–5.CrossRefGoogle ScholarPubMed
Spence, I. M. & Silk, M. H. (1971). Ultrastructure studies of the blood fluke – Schistosoma mansoni. V. The female reproductive system – a preliminary report. South African Journal of Medical Science 36, 4150.Google ScholarPubMed
Verhey, C. A. & Moyer, F. H. (1967). Fine structural changes during sea urchin oogenesis. Journal of Experimental Zoology 164, 195226.CrossRefGoogle Scholar