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Torpedo marmorata acetylcholinesterase; a comparison with the Electrophorus electricus enzyme. Molecular forms, subunits, electron microscopy, immunological relationship.

Electron microscopy, sequential degradation by hydrolytic enzymes and the physical-chemical properties of the molecular forms of Torpedo acetylcholinesterase indicate that these molecules are structurally related to each other in the same way as the molecular forms of Electrophorus acetylcholinesterase: all are derived from a complex structure in which three tetrameric groups of subunits are associated with a rod-like 'tail'. In aged preparations the catalytic subunits are split into fragments in a manner similar to those of Electrophorus acetylcholinesterase. Immunological cross-reaction between both enzymes demonstrates the occurrence of common antigenic sites. The enzymes from the two sources, however, are different in their molecular weights and susceptibility to hydrolytic enzymes. Also, Torpedo acetylcholinesterase does not precipitate with either isologous or heterologous antibodies.

Acetylcholinesterase↗

A tridimensional view of intradermal nevi as revealed by scanning electron microscopy.

When scanning electron microscopy (SEM) was applied to the study of intradermal nevi, interesting tridimensional features were recognized. The free surface of the lesions showed ruffled keratinized cells. "Normal" hairs as well as "corkscrew" hairs emerged from the follicular openings. Nevus cells were either round or elongated and surrounded by connective tissue fibers.

Adult↗

Coliphage P1 morphogenesis: analysis of mutants by electron microscopy.

We used electron microscopy and serum blocking power tests to determine the phenotypes of 47 phage P1 amber mutants that have defects in particle morphogenesis. Eleven mutants showed head defects, 30 showed tail defects, and 6 had a defect in particle maturation (which could be either in the head or in the tail). Consideration of previous complementation test results, genetic and physical positions of the mutations, and phenotypes of the mutants allowed assignment of most of the 47 mutations to genes. Thus, a minimum of 12 tail genes, 4 head genes, and 1 particle maturation gene are now known for P1. Of the 12 tail genes, 1 (gene 19, located within the invertible C loop) codes for tail fibers, 6 (genes 3, 5, 16, 20, 21, and 26) code for baseplate components (although one of these genes could code for the tail tube), 1 (gene 22) codes for the sheath, 1 (gene 6) affects tail length, 2 (genes 7 and 25) are involved in tail stability, and 1 (gene 24) either codes for a baseplate component or is involved in tail stability. Of the four head genes, gene 9 codes for a protein required for DNA packaging. The function of head gene 4 is unclear. Head gene 8 probably codes for a minor head protein, whereas head gene 23 could code for either a minor head protein or the major head protein. Excluding the particle maturation gene (gene 1), the 12 tail genes are clustered in three regions of the P1 physical genome. The four head genes are at four separate locations. However, some P1 head genes have not yet been detected and could be located in two regions (for which there are no known genes) adjacent to genes 4 and 8. The P1 morphogenetic gene clusters are interrupted by many genes that are expressed in the prophage.

Chromosome Mapping↗

Ferritin in Crohn's disease tissue: detection by electron microscopy.

Using immune electron microscopy, an attempt has been made to visualise viral particles in Crohn's disease tissue and faeces. No particles resembling viruses were observed, but in the absence of a specific antiserum a negative result does not exclude the presence of a virus, particularly if it is sparsely distributed. Compared with controls, an abundance of a 12 nm particle was found in all Crohn's disease tissue and one small intestinal lymphoma. This particle has been identified as ferritin and is unlikely to be of aetiological significance.

Colon↗

Freeze-drying from tertiary butanol in the preparation of endocardium for scanning electron microscopy.

The scanning electron microscope appearances and shrinkage of blocks of canine endocardium prepared by freeze-drying directly, by freeze-drying after replacing tissue water with tertiary butanol (2-methyl propan-2-ol) and by critical point drying were compared. All three methods demonstrated endothelial cells which showed nuclear prominences, microvilli and intercellular boundaries. The microvilli varied in size and number from dog to dog but were generally less well defined in specimens freeze-dried from water. Shrinkage due to t-butanol dehydration was significantly less than that which occurred in ethanol in the critical point drying method. Overall the reduction in surface area was significantly less in specimens freeze-dried directly at -65 C (6.8%) than in those dried from t-butanol at -20 C (15.4%) and those prepared bly critical point drying (22.1%). However the amount of shrinkage observed in t-butanol treated tissue was not significantly different from that which was critical point dried. It was not possible to distinguish between comparable samples prepared by these two methods on the basis of their scanning electron microscopic appearances. Thus the relative simplicity and convenience of the t-butanol method, together with its saving of time, its use of standard freeze-drying equipment and the avoidance of ice-crystal artefact justify its consideration as an alternative method of preparing wet biological tissue for scanning electron microscopy.

Animals↗

Preliminary report: laboratory-induced stain removal as assessed by environmental scanning electron microscopy.

Environmental scanning electron microscopy (ESEM) was employed to observe stain removal during brushing with Arm & Hammer Dental Care and Crest Regular Toothpaste. ESEM allows serial examinations of the same sample, and does not require a destructive preparative process. Three extracted molars were cleaned, placed into a 96-hour broth culture of Streptococcus mutans, and stain was produced with undiluted chlorhexidine rinse, concentrated coffee and tea for a period of 23 days. After staining, the teeth were examined by ESEM, then brushed using a toothbrushing machine. Imaging was repeated after 5, 10, 15 and 30 seconds of brushing. As seen with ESEM, the Arm & Hammer product had different effects than those from the distilled water control, suggesting something other than that expected from abrasive and mechanical forces alone. There were also differences from the Crest dentifrice removal on this single sample, suggesting a possible difference between the two products. Further studies are needed to confirm and explain these effects.

Chlorhexidine↗

[Diagnostic transmission electron microscopy].

BACKGROUND: Transmission electron microscopy (TEM) is an important diagnostic tool in surgical pathology. MATERIAL AND METHODS: We give an overview, based on our own experience, of the application of TEM in diagnostic pathology. RESULTS: In spite of its potential for high-grade resolution, the actual use of TEM in diagnostic pathology is rather limited. TEM is mandatory in the examination of kidney and muscle biopsies and is often indicated when a metabolic disease is suspected. However, in many centres its importance in tumour pathology has declined because of the advances in the field of immunohistochemistry. TEM requires a great deal of resources and high levels of skills in tissue processing and diagnostic interpretation. INTERPRETATION: The TEM diagnosis must be integrated with light microscopical and, often, immunohistopathological findings, as well as with the clinical data. We therefore recommend close collaboration between the clinician and the laboratory with regard to biopsy indication, handling of samples, and the final diagnosis.

Humans↗

[Morphology of the kidneys in children with primary nephrotic syndrome (lipoid nephrosis) before and after hormone therapy, studied by biopsy (light and electron microscopy)].

Light and electron microscopies were employed to examine biopsy specimens from 15 children suffering from the primary nephrotic syndrome with minimal alterations in renal bodies. The studies were carried out at the height of the disease and in the stage of a clinical remission after prednisolone therapy. The author describes the development of ultrastructural changes in the glomerular filter, primarily of those in podocytes, under the conditions of highly selective proteinuria as well as during hormonal therapy that favours reparative processes and discontinuation of protein "leakage". It is assumed that the anionic layer of the glycocalyx of podocyte pedicles and l. rara ext. heparan sulfates of the basal membrane may play a role in the origin of selective proteinuria.

Child↗

[Results of implantation of teflon paste into the vocal cord according to the data of light and electron microscopy].

Light and electron microscopy was used to study 5 observations of the tissue response to the teflon paste implanted into the vocal cords to modulate the vocal function. The study showed that teflon was not an absolutely inert substance, it produced inflammation as giant cell granuloma of foreign bodies. Giant cells of foreign bodies (GCFB) enclosing and resorbing the particles of teflon were found to have all the ultrastructural signs of actively phagocytizing cells presenting with various differentiation. The ultrastructure of GCFB provides support for the fact that the cells making up polykaryons belong to the system of mononuclear phagocytes.

Female↗

Changes in the diabetic choroidal vasculature: scanning electron microscopy findings.

Scanning electron microscopy (SEM) was used to study vascular casts of 20 cadaver eyes according to our previously described technique. All eyes were taken from patients with long-standing diabetes mellitus type I. The SEM findings in the choroidal vessels included: increased tortuosity, dilation and narrowing, hypercellularity, vascular loop and microaneurysm formation, "drop-out" of choriocapillaries, and sinus-like structure formation between choroidal lobules. To our knowledge, these are the first SEM studies of the vascular casts performed on human cadaver eyes from diabetics.

Adult↗

Normal and collapsed trachea in the dog: scanning electron microscopy study.

Scanning electron microscopy was used to examine canine tracheal cartilage and to determine the relationship between the fibrous and amorphous matrix in this tissue. Collapsed tracheal (CT) cartilage was hypocellular, compared with normal tracheal cartilage. The amorphous matrix of CT cartilage had a porous, fissured texture and did not have the homogeneous appearance of normal tracheal cartilage. Capillaries were seen to pass through CT cartilage. Randomly distributed connective tissue fibers, evident in CT cartilage matrix, were frequently attached to irregular shapes and sizes of amorphous matrix.

Animals↗

[Possibility of the development of cellular structures on the surface of a vascular plexus demonstrated by scanning electron microscopy].

Using scanning electron microscopy, possible ways of the appearance of macrophages on the epithelial surface of the cerebral vascular plexus in rats were studied. The data obtained support the theory which postulates that macrophages are formed in the blood flow or the connective tissue and that subsequently they penetrate through the epithelium of the vascular plexus onto its surface having contact of the cerebrospinal fluid. The structural stages of this process are also reflected in the presented findings.

Animals↗

[Structural study of Mycoplasma by a scanning electron microscopy method].

Scanning electron microscopy was applied to the study of Mycoplasma arthritidis, Myc. gallisepticum, and Acholeplasma laidlawii. Small spherical elements (0.3--0.5 micrometer) formed a reticular "framework" of the colonies in which larger (1--1.5 micrometer) spheroid or irregular-shaped cells (in case of Myc. gallisepticum) and also rod-shaped (1--3 micrometer), filamentous (3--5 micrometer) forms and "large bodies" (5 x 3--8 x 3.5 micrometer) were located. Apparently the latter represented conglomerates of adherent spheroid elements that resembled somewhat "large bodies" of L-forms. Small spheroid buds were revealed on the surface of all the elements.

L Forms↗

[A method for measuring apatite crystals in human dentine by high resolution transmission electron microscopy].

High resolution electron microscopy now makes it possible to use an original method for measuring biological apatite crystals. The crystals of intertubular sound dentine have an average width of 296 A (standard deviation: 37) and an average thickness of 32 A (standard deviation: 5). During the course of so-called arrested caries, crystals get twice as thick compared to those sound dentine, whereas their width remains unchanged.

Apatites↗

Classification of plastic-embedded rat seminiferous epithelium prior to electron microscopy.

Systematic electron microscopic studies of the changes which take place during the cycle of the rat seminiferous epithelium require that each of the 14 stages of the cycle are identified in the light microscope in plastic-embedded material allowing each stage to be trimmed out separately before the electron microscopic study. The classification of the 14 stages has originally been based on the morphological characteristics seen in paraffin-embedded tissue after PAS-staining. PAS-staining is less effective in plastic-embedded material, and this may be a main reason why electron microscopic findings of the seminiferous epithelium relatively seldom are related to the stages of the cycle. In the present paper a method is described by which the 14 stages of the cycle can be easily identified in the light microscope in plastic-embedded tissue. Some of the stages could be subdivided and a total of 23 stages were distinguished. This constitutes a safe method allowing accurate classification prior to electron microscopic examination of the seminiferous epithelium.

Animals↗

Practical aspects of diagnostic electron microscopy.

The electron microscope technique of negative staining was first used to obtain fundamental information about virus morphology, but in recent years it has developed into a practical method for virus diagnosis. The methods employed are both simple and rapid. The following review discusses in detail the steps that must be taken to obtain good electron microscope preparations and illustrates some of the results that can be obtained.

Humans↗

Identification of neuro-epithelial bodies in rabbit fetal lungs by scanning electron microscopy: a correlative light, transmission and scanning electron microscopic study.

In the present study, neuro-epithelial bodies (NEB) were identified by scanning electron microscopy (SEM) within the bronchial epithelium of near-term rabbit fetuses. The surface features and topography of NEB were correlated by light and transmission electron microscopy. In SEM, the surfaces of NEB were easily visualized in smaller peripheral airways because of paucity of ciliated cells in these regions. The NEB formed crater-like pits, which were lined with microvilli and had smooth-surfaced nonciliated cells around the rim. Stereo-pair photographs revealed that the latter cells protruded above adjacent bronchiolar mucosa. The SEM also revealed that NEB were preferentially located near or at bronchiolar bifurcations. This is the first report of the three-dimensional structure of pulmonary NEB. Their direct contact with the airway lumen, as well as their strategic location in bronchiolar mucosa, support the suggestion that they are intrapulmonary receptors and help to regulate air-flow in peripheral airways.

Animals↗

Conditions critical for optimal visualization of bacteriophage adsorbed to bacterial surfaces by scanning electron microscopy.

The potential of scanning electron microscopy as a tool for the detection of viruses on cell surfaces has been studied using bacteriophage P1 adsorbed to Shigella dysenteriae as a model system. Viral particles were readily detectable by scanning electron microscopy on the surface of infected cells which were fixed with glutaraldehyde followed by postfixation in OsO4 and prepared by critical point drying. The virus-studded surface of the infected cells differed markedly from the relatively smooth surfaces of uninfected control cells. Examination of the same preparations with transmission electron microscopy revealed numerous viral particles adsorbed to the surfaces of infected cells, whereas the control cells were free of viruses as expected. Glutaraldehyde fixation alone did not preserve the surface detail of infected cells: cells adsorbed with viruses were not distinguishable from control cells by scanning electron microscopy although by transmission electron microscopy viruses could be visualized. Air drying from water or absolute alcohol resulted in unsatisfactory preservation as compared to the appearance of infected cells prepared by the critical point method. Thus, scanning electron microscopy is capable of resolving viral particles on cell surfaces, but detection of these particles is completely dependent both on the method of fixation and on the technique of drying used.

Adsorption↗