Origin and cytochemisty of the animal dimple granules in Discoglossus pictus (Anura) eggs.

At the centre of the animal hemisphere of the 1000 micron ovarian oocytes of Discoglossus pictus there is the germinative area, a slightly depressed disc, 700 micron wide. During the passage of the oocyte through the oviduct this area becomes invaginated to form the 'animal dimple', which is the only site where successful sperm entrance can occur. Granules (G) with a central electron-dense core and a peripheral portion containing sparse fibrous material are found in the peripheral cytoplasm of the animal dimple. The origin and the cytochemistry of G's have been investigated. G's originate from Golgi complexes located in the peripheral cytoplasm of the germinative area only. Recently formed G's migrate to the oocyte cortical region, where vesicles appear to participate in G's maturation. The core of G's can be digested by pronase, is negative to a test for acid phosphatase detection, and contains a few polysaccharide complexes. In view of their origin from Golgi complex, their location in the oocytes and their exocytosis upon activation, G's seem to correspond to the typical cortical granules of Anurans. However, they appear to have a macromolecular content different from that of the cortical granules.

[1]  S. Denis‐Donini,et al.  Ultrastructural and lectin binding changes during the formation of the animal dimple in oocytes of Discoglossus pictus (Anura). , 1977, Developmental biology.

[2]  R. Elinson Site of sperm entry and a cortical contraction associated with egg activation in the frog Rana pipiens. , 1975, Developmental biology.

[3]  D. Epel The Program of and Mechanisms of Fertilization in the Echinoderm Egg , 1975 .

[4]  C. Campanella The Site of Spermatozoon Entrance in the Unfertilized Egg of Discoglossus pictus (Anura): An Electron Microscope Study , 1975 .

[5]  J. W. Kelly,et al.  Sulfated acid mucopolysaccharides in the cortical granules of eggs. Effects of quaternary ammonium salts on fertilization. , 1974, Experimental cell research.

[6]  J. Hedrick,et al.  Agglutination of jelly coat and cortical granule components and the block to polyspermy in the amphibian Xenopus laevis. , 1974, Proceedings of the National Academy of Sciences of the United States of America.

[7]  E. Anderson Comparative aspects of the ultrastructure of the female gamete. , 1974, International review of cytology.

[8]  D. Wolf,et al.  Formation and structure of the fertilization envelope in Xenopus laevis. , 1974, Developmental biology.

[9]  J. W. Kelly,et al.  Purification of cortical granules from unfertilized sea urchin egg homogenates by zonal centrifugation. , 1972, Developmental biology.

[10]  P. Benson The biochemistry of development , 1971 .

[11]  W. Anderson Cytochemistry of sea urchin gametes. 3. Acid and alkaline phosphatase activity of spermatozoa and fertilization. , 1968, Journal of ultrastructure research.

[12]  N. E. Kemp,et al.  CORTICAL CHANGES IN GROWING OOCYTES AND IN FERTILIZED OR PRICKED EGGS OF RANA PIPIENS , 1967, The Journal of cell biology.

[13]  S. Wischnitzer,et al.  The ultrastructure of the cytoplasm of the developing amphibian egg. , 1966, Advances in morphogenesis.

[14]  B. Balinsky Changes in the ultrastructure of amphibian eggs following fertilization. , 1966, Acta embryologiae et morphologiae experimentalis.

[15]  Carlotta Taddei,et al.  Aspetti ultrastrutturali del cortex di ovociti di Anfibi , 1965 .

[16]  E. Reynolds THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPY , 1963, The Journal of cell biology.

[17]  P. J. Anderson,et al.  HISTOCHEMICAL METHODS FOR ACID PHOSPHATASE USING HEXAZONIUM PARAROSANILIN AS COUPLER , 1962 .