scholarly journals ELECTRON MICROSCOPE STUDIES ON THE DICTYOSOMES AND ACROBLASTS IN THE MALE GERM CELLS OF THE CRICKET

1956 ◽  
Vol 2 (4) ◽  
pp. 123-128 ◽  
Author(s):  
H. W. Beams ◽  
T. N. Tahmisian ◽  
R. L. Devine ◽  
Everett Anderson

The dictyosome (Golgi body) in the secondary spermatocyte of the cricket appears in electron micrographs as a duplex structure composed of (a) a group of parallel double-membraned lamellae and (b) a group of associated vacuoles arranged along the compact lamellae in a chain-like fashion. This arrangement of ultramicroscopic structure for the dictyosomes is strikingly comparable to that described for the Golgi apparatus of vertebrates. Accordingly, the two are considered homologous structures. Associated with the duplex structure of the dictyosomes is a differentiated region composed of small vacuoles. This is thought to represent the pro-acrosome region described in light microscope preparations. In the spermatid the dictyosomes fuse, giving rise to the acroblast. Like the dictyosomes, the acroblasts are made up of double-membraned lamellae and associated vacuoles. In addition, a differentiated acrosome region is present which, in some preparations, may display the acrosome vacuole and granule. Both the dictyosomes and acroblasts are distinct from mitochondria.

1958 ◽  
Vol s3-99 (46) ◽  
pp. 279-284
Author(s):  
J.T. Y. CHOU ◽  
G. A. MEEK

The three kinds of lipid globules recognizable in the living neurones of Helix aspersa have been examined under the electron microscope. The globules of the kind that can be stained blue with methylene blue during life are seen in electron micrographs as spheres or spheroids, with concentric lamination, after calcium-osmium fixation. After fixation with sucrose-osmium laminated crescentic bodies are seen instead; these appear to be formed by distortion of the ‘blue’ globules. The yellow globules contain electrondense material, and sometimes appear reticular. It is possible that the yellow globules may originate by transformation of some of the ‘blue’ globules. The colourless globules generally appear as crenated objects; this appearance may be a shrinkage artifact. Apart from the mitochondria and the three kinds of lipid globules described, no other object large enough to be identified with the light microscope has been seen in the cytoplasm.


1969 ◽  
Vol 43 (2) ◽  
pp. 289-311 ◽  
Author(s):  
P. Whur ◽  
Annette Herscovics ◽  
C. P. Leblond

Rat thyroid lobes incubated with mannose-3H, galactose-3H, or leucine-3H, were studied by radioautography. With leucine-3H and mannose-3H, the grain reaction observed in the light microscope is distributed diffusely over the cells at 5 min, with no reaction over the colloid. Later, the grains are concentrated towards the apex, and colloid reactions begin to appear by 2 hr. With galactose-3H, the reaction at 5 min is again restricted to the cells but it consists of clumped grains next to the nucleus. Soon after, grains are concentrated at the cell apex and colloid reactions appear in some follicles as early as 30 min. Puromycin almost totally inhibits incorporation of leucine-3H and mannose-3H, but has no detectable effect on galactose-3H incorporation during the 1st hr. Quantitation of electron microscope radioautographs shows that mannose-3H label localizes initially in the rough endoplasmic reticulum, and by 1–2 hr much of this reaction is transferred to the Golgi apparatus. At 3 hr and subsequently, significant reactions are present over apical vesicles and colloid, while the Golgi reaction declines. Label associated with galactose-3H localizes initially in the Golgi apparatus and rapidly transfers to the apical vesicles, and then to the colloid. These findings indicate that mannose incorporation into thyroglobulin precursors occurs within the rough endoplasmic reticulum; these precursors then migrate to the Golgi apparatus, where galactose incorporation takes place. The glycoprotein thus formed migrates via the apical vesicles to the colloid.


1961 ◽  
Vol 11 (3) ◽  
pp. 571-605 ◽  
Author(s):  
G. Majno ◽  
G. E. Palade

The mechanism, whereby histamine and serotonin increase the permeability of blood vessels, was studied in the rat by means of the electron microscope. The drugs were injected subcutaneously into the scrotum, whence they diffused into the underlying (striated) cremaster muscle. An intravenous injection of colloidal HgS was also given, in order to facilitate the identification of leaks by means of visible tracer particles. After intervals varying from 1 minute to 57 days the animals were killed; the cremaster was fixed, embedded in methacrylate, and examined with the electron microscope. One to 12 minutes after the injection, the blood vessels of the smallest caliber (3 to 5 micra as measured on electron micrographs) appeared intact. Numerous endothelial openings were present in blood vessels with a diameter of 7 to 8 micra or more. These gaps were 0.1 to 0.8 micra in width; portions of intercellular junctions were often present in one or both of the margins. The underlying basement membrane was morphologically intact. An accumulation of tracer particles and chylomicra against the basement membrane indicated that the latter behaved as a filter, allowing fluid to escape but retaining and concentrating suspended particulate matter of the size used. Uptake of tracer particles by endothelial vesicles was minimal. Phagocytosis by endothelial cells became more prominent at 3 hours, but as a secondary occurrence; the pericytes were actively phagocytic at all stages. At the 3-hour stage no leaks were found. The changes induced by histamine and serotonin were indistinguishable, except that the latter was more potent on a mole-to-mole basis. In control animals only small accumulations of tracer particles were found in the wall of a number of blood vessels. With regard to the pathogenesis of the endothelial leaks, the electron microscopic findings suggested that the endothelial cells become partially disconnected along the intercellular junctions. Supporting evidence was provided at the level of the light microscope, by demonstrating—in the same preparation—the leaks with appropriate tracer particles1, and the intercellular junctions by the silver nitrate method. The lipid nature of the chylomicron deposits observed in electron micrographs was also confirmed at the level of the light microscope, using cremasters fixed in formalin and stained in toto with sudan red.


1966 ◽  
Vol 165 (998) ◽  
pp. 136-154 ◽  

A histological and ultrastructural study was made of the testes of rats, aged 1 to 15 days, which had received partial-body X-irradiation ( ca . 100 r) on the day of birth. Nineteen serially sectioned testes were subjected to a quantitative analysis including counts of germ cells and measurements of nuclear volume. The type, position and general form of germ cells, together with the incidence of various organelles, was assessed semi-quantitatively from 533 electron micrographs of irradiated (370) and normal (163) tissues. Exposure to 100 r at birth has no marked effect on the total population of germ cells during the first 5 days. The transformation of gonocytes into transitional cells is not affected. Subsequently, the treated testes differ from those of coeval controls by the almost complete absence of germinal mitoses and, consequently, of spermatogonia type A. Many of the transitional cells grow into irregularly-shaped giant cells, usually with a highly lobed nucleus and enlarged nucleoli. Although some cells show condensation of chromatin which may indicate the onset of mitotic prophase, the majority appear to degenerate at interphase. By 10 days, the testes contain only a fraction of the original population of germ cells. No significant changes are detectable in the ultrastructure of germ cells up to 4 days after irradiation. The treatment only induces the sporadic appearance of two minor features (pinocytotic vesicles containing electron-dense material; peripheral granular bodies with some internal organization) which are normally absent from corresponding cells in the controls. Electron micrographs of giant transitional cells confirmed the cytological observations of irregularity of nuclear outline and nucleolar enlargement. The nucleoli are frequently irregular in shape and contain material of two distinct electron densities. In general, the organelles of giant transitional cells are normal and healthy in appearance. With advancing age, an increasing proportion of germ cells show degenerative changes leading to pyknosis. Dead cells appear to be engulfed by neighbouring somatic cells. In both normal and irradiated testes, the simple form of Golgi apparatus in the gonocyte changes to a more complex type in the transitional cells. The persistence of giant cells is associated with a tendency for the Golgi apparatus to revert to the simple type, or to disperse into a number of small simple units. The most striking feature is the relatively high incidence of centrioles, suggesting that radiation-induced mitotic inhibition and gigantism may be accompanied by endomitosis. Irradiation does not markedly affect the appearance and incidence of A- and B-bodies (Franchi & Mandl 1964). These organelles tend, however, to persist over a longer period in irradiated than in untreated young rats.


2000 ◽  
Vol 63 (2) ◽  
pp. 409-416 ◽  
Author(s):  
John G. Bartell ◽  
Douglas A. Fantz ◽  
Tia Davis ◽  
Michael J. Dewey ◽  
Malathi K. Kistler ◽  
...  

Electron microscope studies reveal that the undischarged nematocyst thread is not (as the light microscope image suggests) a cylinder containing a compact mass of barbs, but a screw, as first shown in the electron micrographs of Bretschneider (1949). In the process of discharge, the screw surface is converted to a cylinder without significant change in surface area. This transformation is markedly anisometric, the length of the thread increasing almost threefold, while the overall increase in diameter is less than 50 %. The screw shape of the undischarged thread is due to the presence of three helical pleats in the membrane; and discharge results in the smoothing out of these. The cavity of the thread is smaller in the undischarged condition—because of the presence of pleats—and is largely filled by the whorls of asymmetrical barbs (three to a whorl); the tips of the barbs are pressed closely together, while their spatulate bases are distributed in open hexagonal array over the pleated surface of the thread. Barbs readily become detached from the surface of the discharged thread, leaving a complex, striated scar. The discharged thread is a slightly tapering tube in holotrichous isorhizas, and the barbs show systematic changes in size and proportions with taper. Electron micrographs show that the cavity of the undischarged thread is filled with a flocculent material, as is the space between the capsule wall and the thread. This material is presumably the highly hygroscopic proteinaceous working substance responsible for the increase in volume of the capsular fluid—at least up to 200 %—on hydration. The undischarged thread and its contents, isolated under anhydrous conditions, are conspicuously hygroscopic and perform movements of elongation and rotation as water vapour is admitted to or removed from the system. The transformation of a membrane in the form of a screw surface to a cylinder, such as occurs in the discharge of the nematocyst thread, is only possible if portions of the membrane in the trough of the screw increase in area, or portions of the pleats decrease in area. The apparent constancy of the area of the thread throughout discharge suggests that both processes may occur.


1956 ◽  
Vol 2 (3) ◽  
pp. 351-360 ◽  
Author(s):  
Councilman Morgan ◽  
Calderon Howe ◽  
Harry M. Rose ◽  
Dan H. Moore

Representative viruses of the RI-APC group were observed with the electron microscope in thin sections of infected HeLa cells. The viral particles varied in density, were approximately 60 mµ in diameter and had a center to center spacing when close packed of about 65 mµ. Many of the less dense particles exhibited an internal body averaging 24 mµ in diameter. It was suggested that within the nucleus the virus differentiated from dense granular and reticular material and formed crystals. Disintegration of the crystals and disruption of the nuclear membrane with release of virus into the cytoplasm appeared to occur at any stage. No evidence to suggest development of the virus in the cytoplasm was obtained. It was possible to deduce the structure of the viral crystal from the electron micrographs. The viral particles are packed in a cubic body—centered lattice. Correlative histochemical observations in the light microscope which are now in progress revealed that the crystals and non-crystalline aggregates of virus were strongly Feulgen-positive.


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