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Biomedical subjects

H Maisel

Publications and source records attributed to H Maisel.

At least 91 records · Page 5Linked to original sources

The plasma membrane of the rabbit lens cortical fiber. I. Isolation, characterization, and biosynthesis of two membrane intrinsic polypeptides.

Rabbit lens cortical fiber plasma membrane polypeptides were isolated and two membrane intrinsic proteins were characterized by SDS-PAGE. A polypeptide with a molecular weight of 26 kilodaltons is the major constituent of the plasma membrane. The molecular weight and antigenic properties of the other polypeptide studied are similar to polypeptides of cortical water-soluble alpha-crystalline. Biosynthesis of these two polypeptides was studied. After initially high rates, synthesis of both of these polypeptides decreased considerably and maintained a steady rate for the rest of the culture time.

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Chain-proteins of the vertebrate lens.

Some lens proteins exist in a chain-like form in the vertebrate lens fibre cells. They consist of globular proteins arranged on a filamentous backbone.

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Globular bodies: a primary cause of the opacity in senile and diabetic posterior cortical subcapsular cataracts?

We examined 9 cataracts from maturity onset diabetics and 4 senile posterior subcapsular cataracts by scanning electron microscopy, transmission electron microscopy, immunofluorescence for crystallin proteins and actin, histochemical methods and x-ray diffraction. The cataractous regions contained spherical globules up to 20 mu in diameter, often in a fibrous matrix. Some were extracellular Morgagnian globules, apparently formed by blebbing from the cell surface; others appeared to have been formed intracellularly. The area of globular degeneration was usually 300 mu deep, but had deeper fusiform extensions. Morphological changes in the cell cytoplasm varied according to their depth in the cataract. Electron microscopy showed intracellular and extracellular globules, many of them were bounded by lipid bilayer membranes. Immunofluorescent staining showed that all the globules contained gamma-crystallin; some contained alpha- and beta-crystallins and actin. All the globules contained higher concentrations of cysteine or cystine than the surrounding lens tissue but they did not react to stains for carbohydrate or calcium. X-ray diffraction studies showed that crystalline calcium salts were absent. Globules and cavities averaged 45% of the total area in cross section. Assuming an area of cataract to be 300 micron thick and that globules 1 mu in diameter scattered, while 2--20 mu in diameter reflected light, we calculated that light passing through such a thickness would be reduced by 65%. Thus the globules could account for most of the opacity of the cataractous area. Presumably the fibrous degeneration of the cells causes enough light scattering to account for the remainder of the reduction. Cataract patients complain of decreased visual acuity, a golden halo around objects, and difficulties when driving while facing oncoming traffic at night. These probably result from light scattering. In our previous experiments, globular bodies containing gamma-crystallin were found in cells grown in tissue culture, and blebs with increased acitn content similar to Morgagnian globules were formed in tissue culture by treating differentiated rat lens cells of stage 2 by cytochalasin D (which impaired microfilament function). These results suggest the possibility of simulating in tissue culture the morphological alterations seen in the cataractous cell.

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An immunofluorescent study of cornea development in the chick.

The developmental pattern of appearance of a structural corneal antigenic determinant was studied by immunofluorescent methods. It was first detected in the primary corneal stroma at stage 23, and thereafter spread throughout the primary and secondary stroma. This antigen was absent from Bowman's membrane at its initial stage of development, suggesting that this membrane is a new structure in corneal morphogenesis, and not simply a modification of the primary stroma. This study also suggests that the antigenic determinant is a carbohydrate and is secreted by the corneal epithelial cells.

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