Ultrastructural aspects of oocyte growth in the marsupial Monodelphis domestica (grey short-tailed opossum).

Abstract

The growth of the opossum Monodelphis oocyte does not correspond to the strict biphasic pattern so far described in eutherians and marsupials. The oocyte increases appreciably in size during the last stage of antral follicle development. During the primordial and primary follicle stage Balbiani bodies or paranuclear complexes are not detectable in Monodelphis oocytes. Organelles are randomly distributed. In addition to the nucleolus, perichromatin and ribonucleoprotein particles are other intranuclear structures which occur as regular components in the early Monodelphis oocyte. Clusters of particles are mostly seen in close association with the nuclear envelope. Similar material has been encountered in the cytoplasm as a type of freely-existing 'nuage' material but never as mitochondria-associated 'nuage' or 'cement'. Both types of particles, intranuclear and cytoplasmic, disappear by the time antral follicle formation begins. Mitochondria are at first of the typical transformed shape seen in most mammalian oocytes. They are large, round or oval in outline with a few, often arched, cristae and a light matrix. During the primary follicle stage, mitochondrial size and complexity decrease and the matrix becomes electron dense. A close relationship between mitochondria and endoplasmic reticulum appears early in the primordial and later in the primary follicle oocyte. Regularly detected structures in the ooplasm of preantrum oocytes are paired or 'confronting' cisternae of endoplasmic reticulum, which are lamellar complexes comprised of 2 or more parallel cisternae with intervening electron-dense material. The most conspicuous inclusions in the Monodelphis oocytes of the tertiary and graafian follicles are vesicles. All other organelles are confined to the peripheral zone of the oocyte. Golgi and endoplasmic vesicles both take part in the formation of multivesicular bodies which seems to be the starting point for the vesicle accumulation. Further increase in size involves the incorporation of endocytotic vesicles and the coalescence of larger vesicles. Ordinary fixation procedure leave the vesicles empty. Cortical granules are found only in small numbers.

Full text

PDF

• 481
• 482
• 483
• 484
• 485
• …
• 498
• Next

Images in this article

Fig. 11
on p.491

Fig. 12
on p.491

Fig. 13
on p.491

Fig. 14
on p.491

Fig. 15
on p.491

Fig. 16
on p.491

Fig. 2
on p.484

Fig. 3
on p.484

Fig. 4
on p.486

Fig. 5
on p.486

Fig. 6
on p.488

Fig. 7
on p.488

Fig. 8
on p.488

Fig. 9
on p.490

Fig. 10
on p.490

Fig. 17
on p.493

Fig. 18
on p.493

Fig. 19
on p.493

Fig. 20
on p.493

Fig. 21
on p.495

Fig. 22
on p.495