scholarly journals Relations between ultrastructure of mitotic spindle and chromosome translocation

2014 ◽  
Vol 50 (4) ◽  
pp. 585-594
Author(s):  
Jadwiga A. Tarkowska
Keyword(s):  
Electron Microscope ◽  
Mitotic Spindle ◽  
Light Microscope ◽  
Chromosome Translocation ◽  
Water Soluble ◽  
Nerium Oleander ◽  
Submicroscopic Structure ◽  
Chromosome Arrangement

Dividing endosperm cells of <em>Haemanthus katherinae</em> Bak. treated with an 0.25 per cent mixture of water-soluble glycosides from <em>Nerium oleander</em> were insepected in a light microscope (LM) and severe disturbances were found in all phases of mitosis. The same cells were observed in the electron microscope (EM) and relations were noted and analysed between the chromosome arrangement and the submicroscopic structure of the mitotuc spindle. The successive steps in the disintegration of the formed spindle are described: fragmentatiun of all microtubules (MTs) starting from the poles, disappearance of non-kinetachore MTs and further the external MTs of the kineto,chore bundle. The central (internal) parallel ones remain the longest at the kinerf,ochares. Oleander glycosides cause disintegration of the existing MTs and prevent formation of new ones. The causes of restitution transformations in the successive phases of mitosis are discussed.

scholarly journals Effect of water extract from leaves of Nerium oleander L. on mitosis

2015 ◽  
Vol 40 (4) ◽  
pp. 623-631
Author(s):  
J. A. Tarkowska
Keyword(s):  
Electron Microscope ◽  
Allium Cepa ◽  
Mitotic Spindle ◽  
Water Extract ◽  
Water Soluble ◽  
Nerium Oleander ◽  
Root Tips ◽  
Meristematic Cells ◽  
Effect Of Water

The effect of water extract from leaves of <i>Nerium oleander</i> L. on the mitosis in meristematic cells of <i>Allium cepa</i> L. root tips has been studied. Observations were made on the changes during incubation and postincubation. Significant disturbances were observed in the development of the mitotic spindle leading to the formation of polyploid and hypoploid nuclei capable of further division. Substances contained in the water extract, and causing the disturbances, are water soluble glycosides. Introductory observations under an electron microscope indicate that the glycosides desorganize the continuous fibres of the spindle which can be considered as the direct cause of the observed disturbances.

Selective Staining of Acid Mucopolysaccharides By Ruthenium Red

1968 ◽  
Vol 26 ◽  
pp. 38-39
Author(s):  
J. H. Luft
Keyword(s):  
Electron Microscope ◽  
Light Microscopy ◽  
Light Microscope ◽  
Osmium Tetroxide ◽  
Single Cells ◽  
Ruthenium Red ◽  
Collagen Fibers ◽  
Selective Staining ◽  
Pectic Substances ◽  
Solid Tissues

Ruthenium red is one of the few completely inorganic dyes used to stain tissues for light microscopy. This novelty is enhanced by ignorance regarding its staining mechanism. However, its continued usefulness in botany for demonstrating pectic substances attests to selectivity of some sort. Whether understood or not, histochemists continue to be grateful for small favors.Ruthenium red can also be used with the electron microscope. If single cells are exposed to ruthenium red solution, sufficient mass can be bound to produce observable density in the electron microscope. Generally, this effect is not useful with solid tissues because the contrast is wasted on the damaged cells at the block surface, with little dye diffusing more than 25-50 μ into the interior. Although these traces of ruthenium red which penetrate between and around cells are visible in the light microscope, they produce negligible contrast in the electron microscope. However, its presence can be amplified by a reaction with osmium tetroxide, probably catalytically, to be easily visible by EM. Now the density is clearly seen to be extracellular and closely associated with collagen fibers (Fig. 1).

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
Keyword(s):  
Electron Microscope ◽  
Golgi Apparatus ◽  
Electron Micrographs ◽  
Germ Cells ◽  
Light Microscope ◽  
Golgi Body ◽  
Duplex Structure ◽  
Male Germ Cells ◽  
Secondary Spermatocyte ◽  
A Chain

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.

Marine fungi from Seychelles. I. Nimbospora effusa and Nimbospora bipolaris sp. no v. from driftwood

1985 ◽  
Vol 63 (3) ◽  
pp. 611-615 ◽  
Author(s):  
Kevin D. Hyde ◽  
E. B. Gareth Jones
Keyword(s):  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
Light Microscope ◽  
Marine Fungi ◽  
Undescribed Species ◽  
Scanning Electron

Collections of filamentous marine fungi in Seychelles included Nimbospora effusa Koch and an undescribed species, Nimbospora bipolaris Hyde & Jones sp. nov. Tha latter differs from N. effusa in the size of the ascospores and in ascospore appendage morphology. Both species are illustrated by light microscope and scanning electron microscope micrographs.

The Ultra-fine Structure of Lipid Globules in the Neurones of Helix aspersa

1958 ◽  
Vol s3-99 (46) ◽  
pp. 279-284
Author(s):  
J.T. Y. CHOU ◽  
G. A. MEEK
Keyword(s):  
Methylene Blue ◽  
Fine Structure ◽  
Electron Microscope ◽  
Electron Micrographs ◽  
Light Microscope ◽  
Helix Aspersa

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.

scholarly journals AN ELECTRON MICROSCOPE STUDY OF THE EMBRYOLOGY OF THE INTERCALATED DISC IN THE HEART OF THE RABBIT

1957 ◽  
Vol 3 (2) ◽  
pp. 193-202 ◽  
Author(s):  
Alan R. Muir
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Cardiac Muscle ◽  
Microscope Study ◽  
Light Microscope ◽  
Electron Microscope Study ◽  
Muscle Cells ◽  
Intercalated Disc ◽  
Adult Cell ◽  
Embryonic Muscle

Prenatal and postnatal cardiac muscle from rabbits has been studied by electron microscopy, after osmium fixation and methacrylate embedding. The observations showed that 1. Cell membranes divide the muscle into cellular units from the youngest embryo which was studied (9½ days after coitus) until the adult state. 2. The embryonic muscle cells contain only one nucleus, whereas the adult cell may be multinucleated. 3. At all stages of development, wherever a myofibrillar axis crosses a cellular boundary, the myofilaments are interrupted by an intercalated disc. 4. With age, increase in size and complexity of the discs render them recognisable by the light microscope.

scholarly journals Individual microtubules viewed by immunofluorescence and electron microscopy in the same PtK2 cell

1978 ◽  
Vol 77 (3) ◽  
pp. R27 ◽  
Author(s):  
M Osborn ◽  
RE Webster ◽  
K Weber
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Light Microscope ◽  
Immunofluorescence Microscopy ◽  
Uranyl Acetate ◽  
Tubulin Antibodies ◽  
Ptk2 Cell ◽  
Cytoplasmic Microtubules ◽  
Triton X ◽  
Microtubular Structures

PtK2 cells were grown on gold grids and treated with Triton X-100 in a microtubule stabilizing buffer. The resulting cytoskeletons were fixed with glutaraldehyde and subjected to the indirect immunofluorescence procedure using monospecific tubulin antibodies. Grids were examined first by fluorescence microscopy, and the display of fluorescent cytoplasmic microtubules was recorded. The grids were then stained with uranyl acetate and the display of fibrous structures recorded by electron microscopy. Thus the display of cytoplasmic microtubular structures in the light microscope and the electron microscope can be compared within the same cytoskeleton. The results show a direct correspondence of the fluorescent fibers in the light microscope with uninterrupted fibers of diameter approximately 550 A in the electron microscope. This is the diameter reported for a single microtubule decorated around its circumference by two layers of antibody molecules. Thus under optimal conditions immunofluorescence microscopy can visualize individual microtubules.

SEM OBSERVATIONS ON 'TAWARA-SHIBO' (A SERIES OF SWELLINGS ALONG THE AXIS) STEMS OF CHAMAECYPARIS OBTUSA

IAWA Journal ◽  
2002 ◽  
Vol 23 (1) ◽  
pp. 83-96 ◽  
Author(s):  
Ryogo Nakada ◽  
Kaichiro Kawamura
Keyword(s):  
Growth Rate ◽  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
Growth Rates ◽  
Light Microscope ◽  
Chamaecyparis Obtusa ◽  
Stem Form ◽  
Anatomical Features ◽  
Hormonal Secretion ◽  
Scanning Electron

The anatomy of tawara-shibo stems of Chamaecyparis obtusa (Siebold & Zucc.) Endl. was observed using a scanning electron microscope (SEM) and a light microscope. Tawara-shibo is a strange stem form with a series of swellings that appear at regular intervals along the stem axis. Multiseriate rays, trabeculae and related structures, and modified tracheids were frequently observed at swollen portions. These features were less frequent at non-swollen portions.We conclude that abnormal cambial activities, occurring at regular longitudinal intervals, cause the formation and development of these three anatomical features and higher growth rates at swollen portions. As a result of differences in growth rate between swollen and non-swollen portions, the stem form of tawara-shibo develops. It is suggested that formation of the characteristics observed in tawara-shibo stems is genetically controlled by hormonal secretion into or within the cambium.

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