scholarly journals INTRANUCLEAR AND CYTOPLASMIC ANNULATE LAMELLAE IN TUNICATE OOCYTES

1965 ◽  
Vol 24 (3) ◽  
pp. 471-487 ◽  
Author(s):  
R. G. Kessel

Electron microscope studies were made on various tunicate oocytes at different stages of growth and development. Both the inner and outer lamellae of the perforated nuclear envelope demonstrate considerable blebbing activity. The blebs of the inner lamella detach into the nucleoplasm where they undergo a special type of fusion process resulting in the formation of numerous, usually single, differentiated annulate lamellae of various lengths. The blebbing of the outer layer of the nuclear envelope contributes to the vesicular and granular endoplasmic reticulum characteristically present in the ooplasm and perhaps to the differentiation of cytoplasmic annulate lamellae as well. Cytoplasmic stacks of annulate lamellae frequently have ribosomes associated with them. In addition, granular accumulations are sometimes observed around or between the annuli. The morphological evidence suggests that, at least in many cases, the annuli in the annulate lamellae are patent.

1972 ◽  
Vol 55 (3) ◽  
pp. 533-541 ◽  
Author(s):  
Bela J. Gulyas

The formation of the blastomere nucleus was examined in the rabbit zygote with the electron microscope. In late anaphase the chromosomes are bare and vesicles of the smooth endoplasmic reticulum are numerous in the vicinity of the chromosomes. In early telophase individual chromosomes attain their own nuclear envelope and they are called karyomeres. The envelope of the karyomeres contains small gaps within it at several places where the chromatin is exposed to the cytoplasm. Nuclear pores are also observed. In the cytoplasm short annulate lamellae appear adjacent to the karyomeres, and clusters of punctate substance are also present. From early telophase onward the karyomeres extend pseudopod-like structures, called karyopods, which extend toward other karyomeres or karyopods, and consequently fuse together and serve as chromosomal bridges. Eventually all of the karyomeres fuse into a dense nucleus and decondensation of the chromosomes occurs.


Development ◽  
1982 ◽  
Vol 70 (1) ◽  
pp. 153-169
Author(s):  
Hiroshi Imoh

The distribution of annulate lamellae, electron-dense masses, rough endoplasmic reticulum, and Golgi complexes in longitudinal sections of newt oocytes at several stages of progesteroneinduced maturation was recorded with an electron microscope equipped with a drawing device. Annulate lamellae in full-grown oocytes occur in close contact with electron-dense masses and the nuclear envelope and elsewhere. Stacks of annulate lamellae increase in number for 6 h after progesterone treatment. Meanwhile, they segregate into three groups. The largest group, comprising about 75% of total stacks, forms a row parallel to and just beneath the oocyte cortex of both the animal and vegetal hemispheres, a second group is distributed in the middle area of the vegetal hemisphere, and a third group appears near the yolk-free cytoplasm formed at the vegetal side of the germinal vesicle during the maturation. About 6 h after progesterone treatment the annulate lamellae begin to disappear at their places of localization and none is found a few hours after germinal vesicle breakdown. No immediate fine-structural change in the cortical area follows the disappearance of subcortical annulate lamellae. The possible origins and fates of annulate lamellae in the maturing newt oocytes are discussed.


1963 ◽  
Vol 19 (2) ◽  
pp. 391-414 ◽  
Author(s):  
Richard G. Kessel

Developing oocytes, ranging from approximately 0.1 to 1.0 mm in diameter, in Necturus were studied with the electron microscope. The outer layer of the nuclear envelope is actively engaged in the formation of vesicular elements along most of its surface, especially in smaller oocytes. Groups of vesicles appear to be released into the ooplasm at about the same time, resulting in long chains of individual vesicles immediately adjacent to the nuclear membrane. This process is repeated so that chains of vesicles grouped in rather ordered ranks extend progressively into the surrounding cytoplasm. Eventually, the cytoplasm becomes more concentrated with chains of vesicles and the distance between the individual rows becomes less. Very soon after a chain of vesicles has been budded off from the nuclear membrane, fine intervesicular connections appear between certain of the vesicles comprising the rows. Several of the vesicles in a row may then fuse, forming short, flattened cisternae. Fusion of vesicles continues, individual rows of vesicles become more closely packed and, finally, regions appear in the cytoplasm which have the appearance of annulate lamellae. Further growth of the lamellae appears to occur by the progressive fusion of vesicles at the ends of those lamellae already present, as well as by the addition of other fusing rows of vesicles.


1959 ◽  
Vol 5 (3) ◽  
pp. 501-506 ◽  
Author(s):  
W. Gordon Whaley ◽  
Hilton H. Mollenhauer ◽  
Joyce E. Kephart

Maize root tips were fixed in potassium permanganate, embedded in epoxy resin, sectioned to show silver interference color, and studied with the electron microscope. All the cells were seen to contain an endoplasmic reticulum and apparently independent Golgi structures. The endoplasmic reticulum is demonstrated as a membrane-bounded, vesicular structure comparable in many aspects to that of several types of animal cells. With the treatment used here the membranes appear smooth surfaced. The endoplasmic reticulum is continuous with the nuclear envelope and, by contact at least, with structures passing through the cell wall. The nuclear envelope is characterized by discontinuities, as previously reported for animal cells. The reticula of adjacent cells seem to be in contact at or through the plasmodesmata. Because of these contacts the endoplasmic reticulum of a given cell appears to be part of an intercellular system. The Golgi structures appear as stacks of platelet-vesicles which apparently may, under certain conditions, produce small vesicles around their edges. Their form changes markedly with development of the cell.


Development ◽  
1968 ◽  
Vol 19 (3) ◽  
pp. 319-326
Author(s):  
Lennart Nicander ◽  
Björn A. Afzelius ◽  
Inger Sjödén

Fertilization is accompanied by changes in the structure of the egg cytoplasm (cf. Rothschild, 1958; Raven, 1961). At the level of fine structure such changes have mainly been studied in some marine invertebrates with small eggs that can easily be fertilized in vitro (Pasteels & de Harven, 1963; Schäfer, 1966). Vertebrate eggs are less favourable in this respect, but electron microscope studies have been made on eggs of mammals (Fléchon, 1966; Zamboni & Mastroianni, 1966; Zamboni, Mishell, Bell & Baca, 1966) and Xenopus (van Gansen, 1966). Changes generally observed soon after fertilization include the formation of polysomes or an increase in their number, a hypertrophy of the Golgi complexes, and the appearance of granulated endoplasmic reticulum and annulate lamellae. Afzelius (1957) observed the dispersal of mitochondria in fertilized sea-urchin eggs. Pasteels & de Harven (1963) reported that the structure and distribution of cytoplasmic organelles in eggs of the bivalve mollusc, Barnea Candida, are not altered by fertilization.


1972 ◽  
Vol 18 (7) ◽  
pp. 997-1002 ◽  
Author(s):  
I. L. Stevenson ◽  
S. A. W. E. Becker

Methods have been developed for the rapid, reproducible induction of high-density populations of F. oxysporum chlamydospores. On transferring washed pregerminated conidia to a simple two-salts medium, chlamydospore morphogenesis was evident by 12 h and masses of mature spores could be harvested at the end of 4 days. Electron-microscope studies of thin sections of mature chlamydospores reveal a thick triple-layered cell wall. The cytoplasm contains, in addition to large lipid deposits, a nucleus, mitochondria, and endoplasmic reticulum all typical of fungal cells. Chlamydospores of F. oxysporum exhibit two distinct types of cell surface in thin section. The outer wall layer of two of the isolates studied was smooth-surfaced while the outer layer of the two other isolates was distinctly fibrillose. Some evidence is presented suggesting that the fibrillose material arises through the partial breakdown of the original hyphal wall.


1968 ◽  
Vol 37 (2) ◽  
pp. 540-550 ◽  
Author(s):  
John W. Everingham

Oocytes of four species of ascidians were examined with the electron microscope. Prior to fixation, oocytes were subjected to centrifugal forces of 10–15,000 g for 5–10 min and were compared with uncentrifuged oocytes. Intranuclear annulate lamellae (IAL) are distributed uniformly around the periphery of the nucleus of the uncentrifuged oocyte. Centrifugation produces a marked flattening of the oocyte nucleus, migration of nucleoli to the centrifugal end, and often a condensation of the nucleoplasm at the centrifugal end. In contrast, the distribution of IAL is unchanged by centrifugation. Furthermore, numerous IAL profiles appear to be touching the nuclear envelope, and, in a few of these, direct continuity of the IAL with the nuclear envelope is demonstrated.


2015 ◽  
Vol 48 (3) ◽  
pp. 381-389
Author(s):  
J. A. Tarkowska

Dividing endosperm cells of <i>Haemanthus katherinae</i> Bak., treated with 0.025 per cent aqueous solution of a mixture of glycosides from <i>Nerium oleander</i> were examined in vitro in the light and in the electron microscope. A high hypertrophy of endoplasmic reticulum was noted. In prometaphase and metaphase, after treatment for about l h 45 min there appeared very narrow cisternae forming various configurations, frequently in parallel and concentric arrangement. On the membranes of these cisternae there are formed dark areas interpreted as pores characteristic for nuclear envelopes, this indicating that at least part of the two-membrane structures transforms to the nuclear envelope. The formation of the new nuclear envelope pre-maturely and apparently in excess is discussed.


1969 ◽  
Vol 5 (3) ◽  
pp. 699-726
Author(s):  
LOWELL E. DAVIS

The differentiation of neurosensory cells in Hydra has been studied at the level of the electron microscope. These cells arise from interstitial cells (undifferentiated cells) and not from pre-existing nerve cells. Furthermore, there is no evidence to suggest that neurosensory cells represent a stage in the development of other nerve cells, i.e. ganglionic and neurosecretory cells. Major cytoplasmic changes in fine structure during differentiation include development of a cilium and associated structures (basal body, basal plate, rootlets), development of microtubules and at least two neurites, increase in Golgi lamellae and formation of dense droplets typical of neurosecretory droplets, structural variations in mitochondria and a decrease in the number of ribosomes. Granular endoplasmic reticulum is characteristically poorly developed in all stages of differentiation, including the mature neurosensory cell. Nuclear and nucleolar changes also occur during differentiation but these are less dramatic than the cytoplasmic events. The possibility of neurosensory cells being bi- or multiciliated and the presence of intercellular bridges between these cells are considered. The function of neurosensory cells is discussed briefly in relation to the function of the cilium and neurosecretory droplets.


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