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E S Snigirevskaia

Publications and source records attributed to E S Snigirevskaia.

At least 19 recordsLinked to original sources
PubMed2006

[Structural-functional organization of Golgi apparatus].

This review is dedicated to the structure and function of Golgi apparatus (GA). It summarizes contemporary data published in numerous experimental papers and in several reviews. Possible ways of intra-Golgi transport of proteins, existent models of structural and functional organization of Golgi organelle, as well as the issues of its biogenesis, posttranslational modification and sorting of proteins and lipids, and mechanisms of their trafficking are discussed. Special attention is paid to the role of coatomer proteins (COPI, COPII and clathrin), fusion proteins (SNAREs), and small GTPases (ARF, SARI) in the secretory pathway. In addition, the phenomena of ultrastructural alterations of GA due to various functional conditions and physiological stimuli are specifically accented. We included in this review our original data on a probable involvement of GA in water transport, and on the organization of atypical GA in microsporidia--intracellular parasitic protists.

Animals↗
PubMed2006

[Structural-functional organization of Golgi apparatus].

This review is dedicated to the structure and function of Golgi apparatus (GA). It summarizes contemporary data published in numerous experimental papers and in several reviews. Possible ways of intra-Golgi transport of proteins, existent models of structural and functional organization of Golgi organelle, as well as the issues of its biogenesis, posttranslational modification and sorting of proteins and lipids, and mechanisms of their traffic-king are discussed. Special attention is paid to the role of coatomer proteins (COPI, COPII and clathrin), fusion proteins (SNAREs), and small GTPases (ARF, SARI) in the secretory pathway. In addition, the phenomena of ultrastructural alterations of GA due to various functional conditions and physiological stimuli are specifically accented. We included in this review our original data on a probable involvement of GA in water transport, and on the organization of atypical GA in microsporidia--intracellular parasitic protists.

Animals↗
PubMed2006

[Structural-functional analysis of diffusion in glucose absorption by rat small intestine enterocytes].

To elucidate mechanisms providing transport of sugars across intestinal epithelium, on taking into account the current hypotheses (active transport, participation of paracellular transport and passive component of transcellular transport), it was important to reveal structural changes of tight junctions and distribution of the carriers of facilitated diffusion of GLUT2 and protein kinase C during absorption of glucose. On using confocal and electron microscopy, ultrastructural and immunocytochemical studies of enterocytes after perfusion of isolated rat small intestine fragment with 75 mM glucose (chronic experiment) have shown: 1) fluorescent labels of transporter GLUT2 and PKCbetaII are located in the apical area of enterocytes situated at the upper half of the villus. Antibodies against GLUT2, conjugated with gold, are revealed at the microvilli or apical membrane and in the area of terminal network; 2) no ultrastructural changes of the tight junction are detected on ultrathin sections and freeze--fracture replics. At the same time, fluorescent and gold labels against actin are concentrated in the vicinity of the lateral membrane in the tight junction area. The results obtained can serve a confirmation of a hypothesis that at high glucose concentrations GLUT2 participates in its transfer across the apical membrane.

Animals↗
PubMed2004

[Immunocytochemical localization of vasopressin at its absorption by cells of rat small intestine].

Morpho-physiological characteristics of the transport of cyclic nonapeptide arginine vasopressin (AVP) across the rat intestinal epithelium was studied in experiments in vitro. A partial absorption of physiologically active AVP was followed when filling the isolated intestinal lumen by hormone solution. By methods of immunoelectron and immunofluorescence confocal microscopy, using polyclonal anti-AVP antibodies, cytoplasmic localization of AVP label was shown in enterocytes. The AVP label was also observed in the intercellular space in the basal area of epithelium. No label was revealed in the intercellular junctions, and no predominant label accumulation was found in any cytoplasmic structures of the epithelial cells. The obtained results are considered as evidence for the transcellular pathway of partial AVP absorption in rat small intestine.

Animals↗
PubMed2003

[Structural and functional analysis of glucose adsorption at high maltose concentrations in the rat small intestine in vivo].

To elucidate the mechanism of glucose absorption at high substrate concentrations, we studied structural and ultrastructural peculiarities of enterocytes arranged at different levels along the intestinal villus. The preparations were obtained from an isolated segment of the rat small intestine after its perfusion with maltose solutions with both low (25 mM) and high (100 mM) concentrations, respectively. Under conditions of chronic experiment at high substrate concentration, an enlargement of intercellular clefts, indicating glucose absorption, occurred in deeper areas of the villus. Besides, also in chronic experiment, we studied kinetics of maltose hydrolysis and derived glucose absorption in the isolated segment of the rat small intestine after its perfusion with maltose at superhigh (up to 200 mM) initial concentrations. Based on these data, a conclusion is made that active transport is the main mechanism of absorption of glucose derived from maltose hydrolysis, operating both at low disaccharide concentrations, and in the range of its superhigh (up to 200 mM) concentrations.

Animals↗
PubMed2002

[Microtubule dynamics in epithelial cells].

Microtubules (MTs) are necessary components of all eukaryotic cells. They fulfill various functions being involved in cell division, ciliar and flagellar beating, cell shape maintaining, organelle distribution in the cell, organization of other cytoskeletal elements. Dynamic features of MTs have been commonly studied in vitro or on undiffirentiated cultured cells by means of molecular and ultrastructural methods. It is generally accepted that the phenomenon of dynamic instability is the major mechanism of MT turnover in the cell. MTs radiate from the centrosome and take part in the distribution of cell organelles. In addition, epithelial, nerve, and skeletal muscle cells contain non-centrosomal MTs. A few hypothesis of their origin have been so far put forward. According to the capture-release hypothesis, MTs are first nucleated on the a centrosome, then release to be driven in various parts of the cell by molecular motors. Some alternative mechanisms of non-centrosomal MT formation are also proposed in literature. For example, the nucleation sites were reported not only in centrosomes but also in other parts of cells, such as the apical membranes of epithelial cells, the nuclear membrane of muscle cells, pigment granule aggregates of melanophores. On studying frog urinary bladder and large intestine epithelial cells the authors observed in these cells numerous non-centrosomal MTs. This makes epithelial cells, good models for analysing structural and dynamic features of non-centrosomal MTs in differentiated cells. For the urinary bladder the pool of specific granules may serve as MT organizing centers. Non-cenrosomal MTs of these cells have big diameters (35-38 nm) and form bundles oriented in the apical-basal axis of the cell. In addition, non-centrosomal MTs of these cells may participate in the transport of specific granules and giant vacuoles that appear under stimulated water flows through the cell.

Animals↗
PubMed2001

[Electron microscopic study of colonic epithelial cells from the grass frog Rana temporaria under different intensity of water absorption].

Three cell types have been revealed in the epithelium of the frog large intestine: granular, mitochondria-rich, and mucosal cells. Under a low water permeability (0.12 +/- 0.10 mkl/(min.cm2)) the distribution of intramembrane particles (IMP) in the apical cell membrane was the same as in the most cell plasma membranes studied with freeze-fracture method. Under rising osmotic permeability and water absorption (0.43 +/- 0.05 mkl/(min.cm2)) the IMP distribution did not change. In these conditions, the quantity of fusion sites between granule membranes and the apical membrane increased, and the intercellular spaces in basolateral epithelial region were diluted. A a low water permeability, in addition to usual microtubules, bundles of noncentrosomal microtubules with associated osmiophilic globules were revealed. A comparative analysis has been made of the present evidence and previously obtained data on the frog urinary bladder epithelium.

Animals↗
PubMed1999

[Aquaporins of plasma membranes of epithelial cells].

The early 90s have brought us a discovery of a new class of membrane proteins--aquaporins with a function of transmembrane water channels. Being genetically closed proteins aquaporins are members of a large family of channel-forming proteins called MIPs (major intrinsic proteins). All aquaporins, except AQP4, are mercury-sensitive. Many aquaporins have been cloned and identified. Polyclonal antibodies grown against some of them promoted numerous studies of aquaporin localization and distribution in animal and plant tissues. Up to the present, 10 and 2 aquaporins have been described in mammalian and amphibian epithelial tissues, respectively. One of described aquaporins, AQP2, whose localization is confined to kidney collecting duct principal cells, has been found to be a hormone-depending water channel. The insertion of apical vesicles bearing AQP2 was shown to be regulated by vasopressin, meanwhile all other aquaporins are inserted into the plasma membrane constitutively. There is a vast evidence showing that the integrity of microtubules is necessary for both pathways of aquaporin insertion. AQP2 is important for normal kidney functioning and AQP2 mutations cause water-balance disorders. On the contrary, the AQP1 mutations are not accompanied by any evident clinical pathology. This review is focused on a discussion of the data so far available on aquaporin distribution in different animal tissues.

Animals↗
PubMed1998

[Current concept of structure and function of the Golgi apparatus. On the 100-anniversary of the discovery by Camillo Golgi].

The paper is a brief review of the current data on the structure and function of the Golgi apparatus since its discovery till the recent investigations, including the works published in 1997. Apart from reviewing the electron microscopy level of the structure of the Golgi apparatus, the data are considered on its molecular and supramolecular organization. The paper analyses critically the proposed mechanisms of the intracellular transport of proteins and their processing and modifications in the Golgi apparatus both in terms of the vesicular theory and in a model based on the gradual maturation of the cis-cistern and its transformation to the trans-cistern (i.e. its propagation from one pole to the other, a so-called "progression"). Experimental data are described, which disagree with the current models of the intracellular transport. Based on the literature and authors' own data, a modified model of the intracellular transport is proposed. This model eliminates, to a degree, the contradictions present in the models discussed above.

Cell Biology↗
PubMed1997

[Analysis of rat enterocyte ultrastructure during glucose absorption].

Electronmicroscopic study of rat enterocytes under glucose load (10-40 mM) has shown some changes of their structure: aggregations of intramembrane particles of the apical membrane in the microvilli region, the dilitation of lateral intercellular spaces below tight junction, the condensation of actin near tight and intermediate junctions. The presence of these changes and almost absolute absence of destructions in tight junctions organization indicate that the main pathway of the isotonic fluid containing glucose across leaky epithelium of rat small intestine is a transcellular one.

Animals↗
PubMed1996

[The ultrastructural characteristics of the epithelial cells in the frog bladder under the action of vasopressin and in a vasopressin-independent increase in permeability for water].

In experiments on isolated frog urinary bladders it has been found that the low basal level of water permeability in the absence of arginine-vasopressin (AVP) could be significantly increased when the serosal solution was changed several times every 15 min for a fresh Ringer solution. The electron microscopic study of these cells by the freeze-fracture technique showed that the enhancement of water permeability by AVP-independent manner was related to the appearance of intramembranous particle aggregates in luminal membrane of granular cell, that are usually observed only under the action of AVP. The immunocytochemical experiments with monoclonal antibodies against actin revealed the similarity in intracellular actin distribution under the action of AVP and AVP-independent increase of water permeability.

Animals↗
PubMed1996

[An ultrastructural study of the apical cytoskeleton of the epithelial cells in the frog bladder with an ADH-dependent and an ADH-independent increase in osmotic permeability].

Immunocytochemical methods of electron and confocal microscopy were applied for studying the primembrane actin cytoskeleton in the frog urinary bladder granular cells, following the two actions: under the increased vasopressin-induced water permeability, and following autacoid removal by multiple changes of the Ringer solution around the serosa. In both cases similar changes have been revealed in the structure of the apical cytoskeleton and, in addition, a decrease in the density of its actin filament distribution was noticed.

Animals↗
PubMed1995

[A morphofunctional analysis of the changes in the Golgi apparatus in the epitheliocytes of the frog bladder under conditions of the vasopressin stimulation of water transport].

Structural and chemical peculiarities of the Golgi apparatus elements in granular cells of the normal frog urinary epithelium and under vasopressin stimulation of water transport have been studied with different electron microscopic methods: standard chemical fixation, prolonged osmification, freeze-substitution, freeze-fracture, immunocytochemistry, and electron-probe X-ray microanalysis. The structure of the main Golgi elements and its derivatives in normal cells and under the stimulation of water transport has been described. The association of microtubules with the Golgi cisternae was shown. Microtubules are supposed to participate in the support of integrity of the Golgi complex (in normal cells). Under stimulated water transport, depolymerization of microtubules seems to occur, resulting eventually in the Golgi fragmentation. Participation of some specific granules, that are the Golgi derivatives, in the increase of apical membrane water permeability has been shown as the insertion of water channels. Besides, under big water flows, the Golgi cis-cisternae were shown to participate in the formation of large vacuoles containing low potassium. A supposition is put forward that these vacuoles may perform an osmoregulative function in the cell, similar to that of contractile vacuoles of Protozoa.

Animals↗
PubMed1993

[Spontaneous and induced permeability of the tight junctions in the bladder epithelium of the frog Rana temporaria].

The spontaneous and induced alterations in paracellular permeability of the isolated frog urinary bladder were studied. For estimation of the tight junction (TJ) permeability, a fluorescent dye uranine was used. No morphological or functional evidences for the TJ opening were found in the autumn-winter period, both in the control and after the osmotic flow stimulation by 25 mg/ml pituitrine (P) or serosal mannitol (200 mM). In the spring, a spontaneous uranine efflux through the bladder wall from the mucosal solution was found in parallel with an increase in the basal water flow and a decrease in the responses of the bladder to P and serosal hypertonicity. At the same time, the intercellular substance remained to be a barrier for water. In the autumn-winter the TJ opening could be induced by adding sulfhydryl reagents, p-chloromercury-phenyl-sulfonic acid (PCMPS) or N-ethylmaleimide (NEM), to the serosal solution. However, NEM was effective only when added to the mucosal solution. The uranine efflux induced by sulfhydryl reagents was accompanied with a marked hydroosmotic flow in parallel with a diminished sensitivity to P, the barrier properties of intercellular substances were lost. As evidenced by electron microscopy, PCMPS induced a gradual destruction of TJ structures, while certain cytoplasmic structures were not affected. The uranine efflux in the autumn-winter frogs could be induced by an artificial osmotic gradient after preincubation of the bladders in the isotonic solution with P. Some possible intracellular mechanisms causing both spontaneous and induced alterations in the TJ permeability are discussed.

Animals↗
PubMed1993

[An analysis of the structural characteristics of the tight junction of the enterocytes of the rat small intestine during nutrient absorption (immunoelectron microscopic research)].

To analyze structural changes of intercellular relationships of the enterocytes during glycine, glucose, and triolein absorption the structural and immunocytochemical methods of electron microscopy were used. The study was carried out on the proximal part of the rat small intestine in acute and chronic experiments. In the acute ones glucose or glycine solutions (both of 10 and 40 mM) or triolein emulsion (0.5%) were inserted into the isolated small intestinal segments for 20 min. In chronic experiments the isolated loop of the small intestine was perfused with glucose solution (40 mM). Then the corresponding pieces of the intestinal tissue were fixed for structural and immunocytochemical studies. Rarely (in 1% of all cases), and only in chronic experiments, structural changes in the tight junctions--"blisters" and dilatations--were found. At the same time the analysis of the spatial distribution of actin filaments showed that during glucose and glycine absorption the antiactin tracers were found not only within microvilli and on the "root" filaments but also in vicinity of the tight junction and between terminal filaments. The results obtained agree with the hypothesis about the possibility of paracellular transport of some nutrients induced by sodium-dependent transport of glucose and glycine.

Amino Acids↗
PubMed1992

[Tubular structures in Mycoplasma gallisepticum and the localization of a tubulin-like protein].

In all the strains of M. gallisepticum investigated, a protein with apparent molecular weight 40 kDa was revealed by immunoblotting with polyclonal anti-calf brain tubulin antibodies and monoclonal anti-chicken alpha-tubulin antibodies. In other 8 investigated Mycoplasma species no positive reactions with the same antibodies were found. The M. Gallisepticum cells were examined under electron microscope on fine serial sections and on some sections going at different angles to the long cell axis. Undermembrane system of tubules was revealed and the intracellular pattern of the tubular structures were reconstructed. The immunoelectron microscopic data suggest that tubulin-like protein may be included into the structures.

Acholeplasma laidlawii↗
PubMed1991

[The participation of intracellular membranes in forming highly permeable domains in the plasma membrane of epithelial cells during the vasopressin stimulation of water transport].

Using different electron microscopic techniques, parallel studies of structural alterations in the apical membrane and specific granules of the frog urinary bladder granular cells were made. The results obtained suggest the participation of granule membranes in the formation of highly permeable domains in the apical membranes. After ADH action, the domains with high water permeability are internalized bringing cell membrane retrieval.

Animals↗