Microradiographic and electron microscopic observations of the enamel-covered dentine in rat molars

Cardiac sarcoplasmic reticulum (SR) is a complex system of intracellular tubules that, due to their small size and juxtaposition to such electron-dense structures as mitochondria and myofibrils, are often inconspicuous in conventionally prepared electron microscopic material. This study reports a method with which the SR is selectively “stained” which facilitates visualizationwith the transmission electron microscope.

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Electron Microscopic Study of the Epithelium of the Seminal Vesicle of Aging Rats

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100050706 ◽

1974 ◽

Vol 32 ◽

pp. 138-139

Author(s):

V. F. Allison ◽

G. C. Fink ◽

G. W. Cearley

Keyword(s):

Cell Growth ◽

Epithelial Cell ◽

Epithelial Cells ◽

Seminal Vesicle ◽

Seminal Vesicles ◽

Epithelial Layer ◽

Epithelial Hyperplasia ◽

Electron Microscopic ◽

Aging Rats ◽

Pseudostratified Epithelium

It is well known that epithelial hyperplasia (benign hypertrophy) is common in the aging prostate of dogs and man. In contrast, little evidence is available for abnormal epithelial cell growth in seminal vesicles of aging animals. Recently, enlarged seminal vesicles were reported in senescent mice, however, that enlargement resulted from increased storage of secretion in the lumen and occurred concomitant to epithelial hypoplasia in that species.The present study is concerned with electron microscopic observations of changes occurring in the pseudostratified epithelium of the seminal vescles of aging rats. Special attention is given to certain non-epithelial cells which have entered the epithelial layer.

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The Growth of Herpesvirus mulatto in Human Fibroblast

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100051232 ◽

1974 ◽

Vol 32 ◽

pp. 244-245

Author(s):

Glennelle Washington ◽

Philip P. McGrath ◽

Peter R. Graze ◽

Ivor Royston

Keyword(s):

Rhesus Monkey ◽

Microscopic Study ◽

Electron Microscopic Study ◽

Peripheral Blood ◽

Human Fibroblast ◽

Rhesus Monkeys ◽

Human Fibroblasts ◽

Electron Microscopic ◽

Specific Antisera ◽

Peripheral Blood Leucocytes

Herpes-like viruses were isolated from rhesus monkey peripheral blood leucocytes when co-cultivated with WI-38 cells. The virus was originally designated rhesus leucocyte-associated herpesvirus (LAHV) and subsequently called Herpesvirus mulatta (HVM). The original isolations were from juvenile rhesus monkeys shown to be free of antibody to rhesus cytomegalic virus. The virus could only be propagated in human or simian fibroblasts. Use of specific antisera developed from HVM showed no relationship between this virus and other herpesviruses. An electron microscopic study was undertaken to determine the morphology of Herpesvirus mulatta (HVM) in infected human fibroblasts.

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Observation of biological macromolecules using various electron microscopic methods

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100081711 ◽

1978 ◽

Vol 36 (2) ◽

pp. 170-171

Author(s):

Mitsuo Ohtsuki ◽

Michael Sogard

Keyword(s):

Electron Microscope ◽

Phase Contrast ◽

Image Interpretation ◽

Density Lipoprotein ◽

Biological Macromolecules ◽

Contrast Effects ◽

Biological Structure ◽

Electron Microscopic ◽

Structural Investigations ◽

Staining Techniques

Structural investigations of biological macromolecules commonly employ CTEM with negative staining techniques. Difficulties in valid image interpretation arise, however, due to problems such as variability in thickness and degree of penetration of the staining agent, noise from the supporting film, and artifacts from defocus phase contrast effects. In order to determine the effects of these variables on biological structure, as seen by the electron microscope, negative stained macromolecules of high density lipoprotein-3 (HDL3) from human serum were analyzed with both CTEM and STEM, and results were then compared with CTEM micrographs of freeze-etched HDL3. In addition, we altered the structure of this molecule by digesting away its phospholipid component with phospholipase A2 and look for consistent changes in structure.

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Localization of immunolabels by electron microscopy and image averaging

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100075208 ◽

1983 ◽

Vol 41 ◽

pp. 282-283

Author(s):

J. Frank ◽

P.-Y. Sizaret ◽

A. Verschoor ◽

J. Lamy

Keyword(s):

Electron Microscopy ◽

Single Particle ◽

Attachment Site ◽

Uranyl Acetate ◽

Limulus Polyphemus ◽

Resolution Limit ◽

Electron Microscopic ◽

Image Averaging ◽

Top View ◽

Better Than

The accuracy with which the attachment site of immunolabels bound to macromolecules may be localized in electron microscopic images can be considerably improved by using single particle averaging. The example studied in this work showed that the accuracy may be better than the resolution limit imposed by negative staining (∽2nm).The structure used for this demonstration was a halfmolecule of Limulus polyphemus (LP) hemocyanin, consisting of 24 subunits grouped into four hexamers. The top view of this structure was previously studied by image averaging and correspondence analysis. It was found to vary according to the flip or flop position of the molecule, and to the stain imbalance between diagonally opposed hexamers (“rocking effect”). These findings have recently been incorporated into a model of the full 8 × 6 molecule.LP hemocyanin contains eight different polypeptides, and antibodies specific for one, LP II, were used. Uranyl acetate was used as stain. A total of 58 molecule images (29 unlabelled, 29 labelled with antl-LPII Fab) showing the top view were digitized in the microdensitometer with a sampling distance of 50μ corresponding to 6.25nm.

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