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Biomedical subjects

N V Samosudova

Publications and source records attributed to N V Samosudova.

At least 19 recordsLinked to original sources

[Protective role of autotypic contacts under cerebellar neural net injury by toxic doses of NO-generative compounds].

In the present work, cerebellar neural net injury was induced by toxic doses of NO-generative compound (NaNO2). A protective role of glial cells was revealed in such conditions. The present results were compared with those of the previous work concerning the action of high concentration glutamate on the frog cerebellum (Samosudova et al., 1996). In both cases we observed the appearance of spiral-like structures--"wrappers)"--involving several rows of transformed glial processes with smaller width and bridges connecting the inner sides of row (autotypic contact). A statistic analysis was made according to both previous and present data. We calculated the number and width of rows, and intervals between bridges depending on experimental conditions. As the injury increased (stimulation in the NO-presence), the row number in "wrappers" also increased, while the row width and intervals between bridges decreased. The presence of autotypic contacts in glial "wrappers" enables us to suppose the involvement of adhesive proteins--cadherins in its formation. The obtained data suggested that the formation of spiral structures--"wrappers" may be regarded as a compensative-adaptive reaction on the injury of cerebellar neural net glutamate and NO-generative compounds.

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[Intracellular localization of calcium in loach embryonic cells at the early gastrula stage].

Intracellular localization of calcium-accumulated structures in the loach embryo cells at the state of early gastrulation was determined by electron microscope histochemical pyroantimonate method. Calcium-precipitate was observed in the nucleus (external and inner membranes, chromatin and nucleolus), and in the cytoplasm (ER, mitochondria and submembrane cortical layer). Our present data show that such cell organelles as nuclear envelope, ER, and mitochondria serve as the basic cellular stores for calcium, confirming the existence of calcium signal system both in the nucleus and in the cytosol.

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[Nitric oxide as a contrast modulator of basic elements of the cytoskeleton].

Early it was shown that nitric oxide induced in the cerebellum neuronal net both degenerative and compensatory-adaptive changes: 1) bouton encapsulation of spines, and 2) spiral wraps formed by glial cell processes around synapses and boutons. All these morphological changes were produced with cytoskeleton involvement. In the present work we have found that a NO-generative compound enhanced the contrast of cytoskeleton elements which depended on the concentration of this compound. The best contrast was observed at 1 mM concentration. The reason of the contrast enhance may be due presumably to protein transition from a soluble to a membrane-bound state. Using the contrast enhance effect we carried out a comparative analysis of cytoskeleton elements (CE) composition. Results of the analysis showed the specificity of CE in different cell structures: bouton, spine, glial cell. The obtained data support our proposal about the leading role of cytoskeleton in compensatory-adaptive morphological changes in extremal conditions.

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[Structural changes in the cytoskeletal actin in cultured muscle cells when the cultures are stimulated by polystyrene latex].

As we reported elsewhere, the addition of polysterol latex (180 nm) to chick muscle culture accelerated several myogenesis stages, such as proliferation and fusion. In the present work we tried to determine the role of cytoskeletal actin in the mechanism of acceleration. The localization of cytoskeletal actin was studied in normal and latex induced cultures with the help of rodamine--phalloidin. The obtained data have shown that latex beads added to the cultural medium brought about acceleration of cell spreading (the number of spread cell was approximately five times more in comparison with the norm) and enhanced the development of actin network (90% of the cell area was filled with stress-fibrils in 20 h, instead of within 1-3 in the norm). It is proposed that muscle cells interact primarily with latex beads in the cultural medium before seeding on the glass. From this point of view latex beads can be considered as a primary substratum. The cell contact with the primary substratum initiates the actin network reorganization that leads to activation of cell spreading with a subsequent acceleration of myogenesis process: adhesion, proliferation and fusion.

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[Ultrastructural characteristics of the pentalaminar contact and its role in myoblast fusion].

Two types of the pentalaminar structure were found in developing skeletal muscles. One of them is characterized by three electron-dense lines 23-25 nm in size. The other one, 11 nm in size, has only one electron-dense central line and forms membrane invaginations (blebs), 100-250 nm in diameter. The transformation of the "bridge" contact into the 2nd type pentalaminar structure and electron-dense bodies--"lenses" (60-65 nm) was established. The "lenses" contain an electron-dense material, similar to that of the "bridges". Neuraminidase hydrolysis shows that the "bridges" consist of glycoproteins. The muscle cells were extracted with 0.5% triton X-100. The detergent removes most of phospholipids. The first type of the pentalaminar structure remains stable to detergent treatment, whereas the second type may be dissolved. Besides, a partial destruction of surface membranes--"breaks"--are observed in the regions of membrane transmission to the pentalaminar structure. The detergent appears to act on those sites of the surface membrane which are instable and ready to fuse, especially on the bases of invaginations.

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[Formation of intercellular contacts in myogenesis].

In myogenesis in vivo and in the muscle tissue culture certain intercellular junctions have been revealed; they differ in their ultrastructure and functions. For the stage of interaction between a myoblast with another myoblast contacts of adhesive type are distinctive: desmosomes and fasciae adherentes. They are necessary for adhesion of the cells with each other. Besides, gap and punctate contacts occur, serving for exchange of metabolites and electrical conjugation. At more advanced stages of fusion, when the myoblast gets into contact with the early muscle tubule, a bridge contact is observed, resembling the septal one, which is able to transform into a pentalayered (tight) junction. The latter type evidently participates in fusion of the membranes of the interacting cells.

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Ultrastructural organisation and the sites of calcium localisation in the lamprey striated muscle.

The present paper examines the ultrastructure of the sarcoplasmic recitulum (SR) and the T system in the striated muscle of the lamprey. The pyroantimonate method was used to visualise the sites of intracellular calcium localisation. Characteristic for the muscle studied are the presence of numerous intricately shaped invaginations on the surface membrane of muscle fibres and peripheral contacts between SR cisternae and the sarcolemma. In addition to calcium localised in the terminal cisternae of SR and N-bands of the I-disk, as typical of vertebrate muscles, a great amount of calcium is present in the subsarcolemmal region, corresponding to the area of invaginations, and in longitudinal elements of SR.

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[Intercellular interactions preceding muscle cell fusion].

Membrane interactions of myogenic cells of the 7-8 old chick embryos were investigated by electron microscopy. Tannic acid was used as specific fixative for biological membranes. Three types of specialized contacts can be revealed in fused myogenic cells: the first is like gap junctions, the second represents a pentalamellar structure, and the third is a so far non-described type of contact showing a membrane complex consisting of two parallel membranes arranged at a distance of approximately 15 nm and connected by electron-dense "bridges". The third type contact is revealed only by tannin-fixation. It is suggested that the "bridge" contact precedes the pentalamellar structure. A transition from the first type of contact to the second one is possible. The pentalamellar structure can be considered as an initial phase of fusion.

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[Disorders of myocardial contraction and cardiomyocyte ultrastructure after emotional stress].

By means of physiological, electron microscopical and histochemical methods, changes in intensity of mechanisms participating in calcium transport and the cations localization in cardiomyocytes have been studied, the changes resulted from an emotional-painful stress. After the stress, the contractile function of the rat isolated heart becomes more dependent on calcium concentration in the perfusate. As demonstrate combined electron microscopical and histochemical methods and, first of all, determination of calcium antimonate in the cardiomyocytes, together with increased cardiac function, an elevated amount of calcium localized in sarcoplasm of cardiomyocytes is observed, especially in the subsarcolemmic area. The data obtained demonstrate that the membrane mechanisms of calcium transport are injured and calcium content in the sarcoplasm is increased; that can play a definite role in the development of focal lesions in the myocardium at a stress.

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[Calcium localization in the degenerating myotubes of developing skeletal muscle in the chick embryo].

Ca-accumulating formations found in degenerating myotubes of chick embryo by pyroantimonate technique have been identified as membrane bound bodies in the material fixed routinely for electron microscopy. These bodies seem to represent initial stages of a lipid degeneration of membranous structures. It is assumed that calcification of single degenerating subcellular structures may limit spreading necrosis over the whole cell.

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[Calcium in the developing skeletal muscles of the chick embryo].

The osmium-pyroantimonate technique was used for the ultrastructural study of Ca2+-localization in two types of chick embryo skeletal muscles: m. pectoralis and m. soleus. In 8- and 12-day old embryos the pyroantimonate precipitate was found on plasmalemma, condensed chromatine and ribosomes and in N-lines of I-band. During myogenesis (15-, 21-day old embryos) the calcium precipitate is redistributed from the above mentioned sites to terminal cisternae and N-line of I-band. It is proposed that calcium of N-lines may be involved in the glycogenolysis, its association with the muscle contraction occurring particularly at early developmental stages.

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