Using the Chemistry of the Hydroxyl Radical to Determine Structural Details about DNA and Protein-DNA Complexes

There are conflicting reports regarding some fine structural details of arteries from several animal species. Buck denied the existence of a sub-endothelial space, while Karrer and Keech described a space of variable width which separates the endothelium from the underlying internal elastic lamina in aortas of aging rats and mice respectively.The present communication deals with the ultrastrueture of the interface between the endothelial cell layer and the internal elastic lamina as observed in carotid arteries from rabbits of varying ages.

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Annulate lamellae in the Sertoli cells of guinea pig testis after unilateral torsion of the spermatic cord

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100111094 ◽

1984 ◽

Vol 42 ◽

pp. 196-197

Author(s):

J. Chakraborty ◽

A. P. Sinha Hikim ◽

J. S. Jhunjhunwala

Keyword(s):

Sertoli Cells ◽

Guinea Pigs ◽

Spermatic Cord ◽

Present Report ◽

Cell Types ◽

Annulate Lamellae ◽

Spermatogenic Cells ◽

Electron Microscopic ◽

Structural Details ◽

First Time

Although the presence of annulate lamellae was noted in many cell types, including the rat spermatogenic cells, this structure was never reported in the Sertoli cells of any rodent species. The present report is based on a part of our project on the effect of torsion of the spermatic cord to the contralateral testis. This paper describes for the first time, the fine structural details of the annulate lamellae in the Sertoli cells of damaged testis from guinea pigs.One side of the spermatic cord of each of six Hartly strain adult guinea pigs was surgically twisted (540°) under pentobarbital anesthesia (1). Four months after induction of torsion, animals were sacrificed, testes were excised and processed for the light and electron microscopic investigations. In the damaged testis, the majority of seminiferous tubule contained a layer of Sertoli cells with occasional spermatogonia (Fig. 1). Nuclei of these Sertoli cells were highly pleomorphic and contained small chromatinic clumps adjacent to the inner aspect of the nuclear envelope (Fig. 2).

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Detection of viruses by electron microscopy: Increased sensitivity by direct micro-ultracentrifugation of samples

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100128821 ◽

1987 ◽

Vol 45 ◽

pp. 908-909

Author(s):

Alain R. Trudel ◽

M. Trudel

Keyword(s):

Electron Microscopy ◽

Fold Increase ◽

Observation Time ◽

Clinical Samples ◽

Maximum Speed ◽

Viral Particles ◽

Structural Details ◽

Latex Spheres ◽

Increased Sensitivity ◽

Size Of Particles

AirfugeR (Beckman) direct ultracentrifugation of viral samples on electron microscopy grids offers a rapid way to concentrate viral particles or subunits and facilitate their detection and study. Using the A-100 fixed angle rotor (30°) with a K factor of 19 at maximum speed (95 000 rpm), samples up to 240 μl can be prepared for electron microscopy observation in a few minutes: observation time is decreased and structural details are highlighted. Using latex spheres to calculate the increase in sensitivity compared to the inverted drop procedure, we obtained a 10 to 40 fold increase in sensitivity depending on the size of particles. This technique also permits quantification of viral particles in samples if an aliquot is mixed with latex spheres of known concentration.Direct ultracentrifugation for electron microscopy can be performed on laboratory samples such as gradient or column fractions, infected cell supernatant, or on clinical samples such as urine, tears, cephalo-rachidian liquid, etc..

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The restoration of blurred electron micrographs

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100142529 ◽

1986 ◽

Vol 44 ◽

pp. 180-181

Author(s):

Bridget Carragher ◽

David A. Bluemke ◽

Michael J. Potel ◽

Robert Josephs

Keyword(s):

Cross Section ◽

Electron Micrographs ◽

Relative Motion ◽

Finite Thickness ◽

Image Plane ◽

Helical Axis ◽

Thin Sections ◽

Structural Details

We have investigated the feasibility of restoring blurred electron micrographs. Two related problems have been considered; the restoration of images blurred as a result of relative motion between the specimen and the image plane, and the restoration of images which are rotationally blurred about an axis. Micrographs taken while the specimen is drifting result in images which are blurred in the direction of motion. An example of rotational blurring arises in micrographs of thin sections of helical particles viewed in cross section. The twist of the particle within the finite thickness of the section causes the image to appear rotationally blurred about the helical axis. As a result, structural details, particularly at large distances from the helical axis, will be obscured.

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