Transmission electron microscopy Dotaz Zobrazit nápovědu
This study was conducted to investigate Brachymystax lenok tsinlingensis spermatozoa cell morphology and ultrastructure through scanning and transmission electron microscopy. Findings revealed that the spermatozoa can be differentiated into three major parts: a spherical head without an acrosome, a short mid-piece, and a long, cylindrical flagellum. The mean length of the spermatozoa was 36.11±2.84μm, with a spherical head length of 2.78±0.31μm. The mean anterior and posterior head widths were 2.20±0.42μm and 2.55±0.53μm, respectively. The nuclear fossa was positioned at the base of the nucleus that contained the anterior portion of flagellum and a centriolar complex (proximal and distal centrioles). The short mid-piece was located laterally to the nucleus and possessed just one spherical mitochondrion with a mean diameter of 0.65±0.14μm. The spermatozoa flagellum was long and cylindrical, and could be separated into two parts: a long main-piece and a short end-piece. The main piece of the flagellum had short irregular side-fins. The axoneme composed the typical '9+2' microtubular doublet structure and was enclosed by the cell membran e. This study confirmed that B. lenok tsinlingensis spermatozoa can be categorized as teleostean "Type I" spermatozoa; 'primitive' or 'ect-aquasperm type' spermatozoa. To the best of the authers knowledge, this was the first study conducted on the morphology and ultrastructure of B. lenok tsinlingensis spermatozoa.
- Klíčová slova
- Brachymystax lenok tsinlingensis, Morphology, Scanning electron microscopy, Spermatozoa, Transmission electron microscopy, Ultrastructure,
- MeSH
- akrozom ultrastruktura MeSH
- axonema ultrastruktura MeSH
- buněčné jádro ultrastruktura MeSH
- centrioly ultrastruktura MeSH
- flagella ultrastruktura MeSH
- mikroskopie elektronová rastrovací MeSH
- mitochondrie ultrastruktura MeSH
- Salmonidae anatomie a histologie růst a vývoj MeSH
- spermie ultrastruktura MeSH
- transmisní elektronová mikroskopie MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Leachates collected at two (active and closed) municipal solid waste (MSW) landfills were examined for colloids and particles by transmission electron microscopy, energy dispersive spectrometry, selected area electron diffraction and for the chemical compositions of the filtrates after the filtration to 0.1 µm and ultrafiltration to 1 kDa (~ 1 nm). Six groups of colloids/particles in the range 5 nm to 5 µm were determined (in decreasing order of abundance): carbonates, phyllosilicates (clay minerals and micas), quartz, Fe-oxides, organics and others (salts, phosphates). Inorganic colloids/particles in leachates from the active landfill predominantly consist of calcite (CaCO(3)) and minor clay minerals and quartz (SiO(2)). The colloids/particles in the leachates from the closed landfill consist of all the observed groups with dominant phyllosilicates. Whereas calcite, Fe-oxides and phosphates can precipitate directly from the leachates, phyllosilicates and quartz are more probably either derived from the waste or formed by erosion of the geological environment of the landfill. Low amounts of organic colloids/particles were observed, indicating the predominance of organic molecules in the 'truly dissolved' fraction (fulvic compounds). Especially newly formed calcite colloids forming particles of 500 nm and stacking in larger aggregates can bind trace inorganic contaminants (metals/metalloids) and immobilize them in landfill environments.
- MeSH
- koloidy analýza MeSH
- odpadky - odstraňování * MeSH
- transmisní elektronová mikroskopie metody MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- koloidy MeSH
Structure of tench (Tinca tinca L.) spermatozoa was investigated by means of scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Spermatozoa of 26.1+/-3.8 microm total length possessed typical primitive simple structure, called "aqua sperm", without acrosomal head structures. It was probably the smallest spermatozoon described among cyprinid fishes. Heads were mostly composed of dense and slightly granular material, which appeared to be fairly homogeneous except for the occasional appearance of vacuoles. The midpiece remained separated from the flagellum by the cytoplasmic channel; it was cylindric/cone-shaped, 0.86+/-0.27 microm in length and 1.17+/-0.24 microm in width at proximal part. The proximal centriole was located in the "implantation fossa". The distal centriole appeared almost tangential to the nucleus and it functioned as a basal body for the flagellum. It had an orientation of 140 degrees with respect to the distal centriole. The sperm flagellum with 25.45+/-2.47 microm of total length had no any fin. The diameter of the flagellum perpendicular to the plane of the doublet of central microtubules was 173.67+/-20.45 nm and horizontal plane of the central microtubules was 200.71+/-20.45 nm. Peripheral doublets and the central doublet of microtubules measured 23.39+/-3.18 and 35.88+/-4.44 nm in width, respectively. The diameter of a microtubule was only 9.14+/-2.97 nm. A vesicle was attached to the most basal region of the flagellum and located just under plasma membrane of the flagellum.
- MeSH
- akrozom ultrastruktura MeSH
- Cyprinidae * anatomie a histologie MeSH
- flagella ultrastruktura MeSH
- mikroskopie elektronová rastrovací metody veterinární MeSH
- spermie ultrastruktura MeSH
- transmisní elektronová mikroskopie metody veterinární MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Further development of low voltage electron microscopy leads to an aberration correction of the device in order to improve its spatial resolution. The integration of a corrector to a desktop transmission electron microscope with exclusively low-voltage design seems to be a challenging task. The benefits and potential of the Rose hexapole corrector implemented to such a system are critically considered in this paper. The feasibility of miniaturized corrector suitable for desktop LVEM is especially discussed, including the aspect of corrector contribution to chromatic aberration that appears to be crucial. Optimal corrector parameters and resolution limits of such a system are proposed. •Improved spatial resolution•Spherical aberration correction•Permanent magnet transfer lenses.
The nuclear pore complex (NPC) is a large elaborate structure embedded within the nuclear envelope, and intimately linked to the cytoskeleton, nucleoskeleton, and chromatin. Many different cargoes pass through its central channel and along the membrane at its periphery. The NPC is dismantled and reassembly, fully or partially, every cell cycle. In post-mitotic cells it consists of a combination of hyper-stable and highly dynamic proteins. Because of its size, dynamics, heterogeneity and integration, it is not possible to understand its structure and molecular function by any one, or even several, methods. For decades, and to this day, thin section transmission electron microscopy (TEM) has been a central tool for understanding the NPC, its associations, dynamics and role in transport as it can uniquely answer questions concerning fine structural detail within a cellular context. Using immunogold labeling specific components can also be identified within the ultrastructural context. Model organisms such as Saccharomyces cerevisiae are also central to NPC studies but have not been used extensively in structural work. This is because the cell wall presents difficulties with structural preservation and processing for TEM. In recent years, high-pressure freezing and freeze substitution have overcome these problems, as well as opened up methods to combine immunogold labeling with detailed structural analysis. Other model organisms such as the worm Caenorhabditis elegans and the plant Arabidopsis thaliana have been underused for similar reasons, but with similar solutions, which we present here. There are also many advantages to using these methods, adapted for use in mammalian systems, due to the instant nature of the initial fixation, to capture rapid processes such as nuclear transport, and preservation of dynamic membranes.
- Klíčová slova
- C. elegans, Freeze substitution, High-pressure freezing, Immunogold, Plant, Thin section transmission electron microscopy, Yeast,
- MeSH
- jaderný pór MeSH
- mrazová substituce * metody MeSH
- Saccharomyces cerevisiae metabolismus MeSH
- savci MeSH
- sušené kvasnice * MeSH
- transmisní elektronová mikroskopie MeSH
- zmrazování MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
We compared the effects of ambient (350 ppm) and elevated CO(2) concentration (700 ppm) on the size and shape of starch granules in Norway spruce (Picea abies (L.) Karst.) needles during one growing season. Starch granules were isolated from needles by alkaline digestion and analyzed by transmission electron microscopy (TEM) and atomic force microscopy (AFM). Measurements made with a particle size analyzer indicated that starch granules ranged between 0.5 and 10 microm. Granule size and shape varied according to needle developmental stage and CO(2) concentration. Generally, elevated CO(2) concentration increased the size of the starch granules. Fine surface structures (< 10 nm in size) studied by AFM were characterized by the presence of protrusions, furrows and pores.
- MeSH
- mikroskopie atomárních sil MeSH
- oxid uhličitý metabolismus MeSH
- povrchové vlastnosti MeSH
- roční období MeSH
- škrob chemie izolace a purifikace ultrastruktura MeSH
- smrk chemie růst a vývoj metabolismus MeSH
- transmisní elektronová mikroskopie MeSH
- velikost částic MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- oxid uhličitý MeSH
- škrob MeSH
Microtriches on different parts of the scolex and neck of the gangesiine cestode Silurotaenia siluri (Batsch 1786) were studied. The neodermis of the central frontal scolex part (around the rostellar furrow) bears filamentous microtriches only. The lateral frontal part and the parts between and posterior to the suckers cover filamentous and spine-like microtriches. Within the suckers there are short spine-like microtriches with bases enforced by electron-dense ribs. The proximal neck part bears filamentous and spine-like microtriches, the middle part solitary distributed blade-like and spine-like microtriches among filamentous ones, and the distal part blade-like microtriches. The functions of different types of microtriches are discussed.
BACKGROUND: Cryptococcus neoformans is one of the most important human fungal pathogens. Its cells contain rich microtubules required for nuclear division and rich F-actin cytoskeletons for cell division. Disruption of microtubules by a microtubule inhibitor should block nuclear division, and disruption of F-actin by an actin inhibitor should block cell division. We investigated the effects of microtubule and actin inhibitors to find out whether the cytoskeletons of C. neoformans can become a new anti-fungal target for the inhibition of cell division, when examined at the ultrastructural level. METHODS: Cells treated with the microtubule inhibitors vincristine (VIN) and methyl benzimidazole-2-ylcarbamate (BCM) and the actin inhibitor latrunculin A (LA), in yeast extract peptone dextrose medium, were examined by scanning (SEM) and transmission electron microscopy (TEM), and the cell number was counted using a Bürker chamber. RESULTS: After 2 days of inhibition with VIN, BCM or LA, the cells did not divide, but later, resistant, proliferating cells appeared in all samples. With combined microtubule and actin inhibitors (VIN + LA or BCM + LA), cells did not divide during 6 or even 14 days, and no resistant cells originated. TEM showed that the inhibited cells were without cytoplasm and were dead; only empty cell walls persisted with reduced capsules, shown on SEM. CONCLUSION: Combined microtubule and actin inhibitors (VIN + LA or BCM + LA), have lethal effects on C. neoformans cells and no resistant cells originate.
- MeSH
- aktiny antagonisté a inhibitory ultrastruktura MeSH
- benzimidazoly farmakologie MeSH
- bicyklické sloučeniny heterocyklické farmakologie MeSH
- Cryptococcus neoformans účinky léků ultrastruktura MeSH
- karbamáty farmakologie MeSH
- lidé MeSH
- mikroskopie elektronová rastrovací metody MeSH
- mikrotubuly účinky léků ultrastruktura MeSH
- thiazolidiny farmakologie MeSH
- transmisní elektronová mikroskopie metody MeSH
- vinkristin farmakologie MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- aktiny MeSH
- benzimidazoly MeSH
- bicyklické sloučeniny heterocyklické MeSH
- carbendazim MeSH Prohlížeč
- karbamáty MeSH
- latrunculin A MeSH Prohlížeč
- thiazolidiny MeSH
- vinkristin MeSH
Scanning and transmission electron microscopy (TEM) were used to study the histopathological effects of the monogenean Macrogyrodactylus clarii Gussev, 1961 on the gills of the catfish Clarias gariepinus (Burchell). Suction generated during attachment created 'footprints' on host surfaces in which the host tissues were elevated above the general gill surface. 'Footprints' were bordered by four clefts caused by the muscular flaps on the anterior, lateral and posterior margins of the haptor. The hamuli points penetrate the gill tissue but no evidence was found for the insertion of the marginal hooklets. At the site of attachment, host cells adjacent to the lateral flaps often appeared compressed and widely spaced with large intercellular spaces. Desquamation of these surface epithelia was also apparent and some of the widely spaced epithelial cells had pseudopodium-like processes. Cells within the upper surface epithelial layer of the host were vacuolated and necrotic. Ruptured blood capillaries (blood spaces) in the secondary gill lamellae contained atypical compressed erythrocytes, agranular and granular leucocytes and evidence of haemorrhaging. Cells with fibrotic cytoplasm, putative phagocytes and host mucous cells were evidence of a host response at the site of parasite attachment. The possible role of these cells is discussed in relation to host resistance against infection.
- Klíčová slova
- aquatic health, fish disease, histopathology, monogeneans, ultrastructure,
- MeSH
- infekce červy třídy Trematoda parazitologie patologie MeSH
- mikroskopie elektronová rastrovací MeSH
- nemoci ryb parazitologie patologie MeSH
- sumci parazitologie MeSH
- transmisní elektronová mikroskopie MeSH
- Trematoda ultrastruktura MeSH
- žábry patologie ultrastruktura MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
In this focus article, we provide a scrutinizing analysis of transmission electron microscopy (TEM) and dynamic light scattering (DLS) as the two common methods to study the sizes of nanoparticles with focus on the application in pharmaceutics and drug delivery. Control over the size and shape of nanoparticles is one of the key factors for many biomedical systems. Particle size will substantially affect their permeation through biological membranes. For example, an enhanced permeation and retention effect requires a very narrow range of sizes of nanoparticles (50-200 nm) and even a minor deviation from these values will substantially affect the delivery of drug nanocarriers to the tumour. However, amazingly a great number of research papers in pharmaceutics and drug delivery report a striking difference in nanoparticle size measured by the two most popular experimental techniques (TEM and DLS). In some cases, this difference was reported to be 200-300%, raising the question of which size measurement result is more trustworthy. In this focus article, we primarily focus on the physical aspects that are responsible for the routinely observed mismatch between TEM and DLS results. Some of these factors such as concentration and angle dependencies are commonly underestimated and misinterpreted. We convincingly show that correctly used experimental procedures and a thorough analysis of results generated using both methods can eliminate the DLS and TEM data mismatch completely or will make the results much closer to each other. Also, we provide a clear roadmap for drug delivery and pharmaceutical researchers to conduct reliable DLS measurements.
