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M Jacobson

Publications and source records attributed to M Jacobson.

At least 163 records · Page 9Linked to original sources

The superficial cells of the transitional epithelium in the expanded and unexpanded rat urinary bladder. Transmission and scanning electron-microscopic study.

The superficial epithelial layer in the urinary bladder of adult rats was examined, in various states, using the transmission and scanning electron microscopes. A good agreement was obtained between the results of the two methods. When the urinary bladder is unexpanded, the superficial cells show marked bulges into the bladder lumen and the contacts between cells (mainly desmosomes) are displaced deep into the epithelium. The luminal surface is bizarrely bent and large parts of the membrane intrude into the cytoplasm, where they give the appearance of discoid and fusiform vesicles. Between neighboring cells, deep interdigitations are observed. In the scanning electron microscope, the surface of the epithelium appears cauliflower-like and has deep grooves, gullys and folds. When the bladder is expanded, the surface becomes smoother and the contacts between cells move to the surface. The stretched cells are angular in form (5-, 6- or 7-sided) and show great variations in surface area (150-500 mum2). The luminal cell membrane consists of an alternation of asymmetrical areas (120 A thick and 0.2-0.4 mum in length) with normal sections which are 80 A thick. In the scanning electron microscope, these thick areas appear as 4-, 5- or 6-sided plaques with a maximal diameter of 0.4 mum. The borders of the plaques are formed of portions of cell membrane which have a normal thickness and extrude as microcristae into the lumen. This produces a honeycomb appearance on the cell surface.

Animals↗

Light- and electron microscopic investigations of pulmonary tissue after high-frequency positive-pressure ventilation (HFPPV).

Narcotisized dogs were artificially ventilated for periods of two to five hours with HFPPV. During this time the blood gases, pH and bases were controlled. In spite of sufficient oxygenation and CO2-elimination, a metabolic acidosis developed which could not be fully compensated by the addition of buffer solutions. In light and electron microscopy these lungs did not differ significantly from control lungs. Haemorrhages or atelectases were never observed. Type I cells as well as Type II cells in the alveoli are unchanged, i.e. the Type II cells were not depleted but contained numerous typical lamellar bodies with a diameter of 0.4-1 mu. The blood gas barrier was not widened and was ca. 3000 A wide. The alveolar surface was coated by an often fragmented electron-dense film (monolayer of the surfactant).

Acid-Base Equilibrium↗

Specification of positional information in retinal ganglion cells of Xenopus laevis: intra-ocular control of the time of specification.

Programming events in the stage 28-31 clawed frog embryo partly determine the organization of the future retinotectal map by specifying the permanent reference axes for cellular positional information in the retina. Thus, when transplanted in 180 degrees -rotated orientation into a stage 27/28 orbit, an unspecified (stage 28 or younger) eye can acquire new axes and develop a normally-oriented retinotectal map, whereas a specified (stage 31 or older) eye retains its original axes and develops an inverted map. We have used the retinotectal map to determine when (and under what conditions) specification with changes in orientation occurred in eye primordia serially transplanted between embryos of different stages. Specification was not precipitated when stage 22/23 eyes were grafted into stage 28-32 embryos or explanted in vitro, nor was specification delayed when stage 28 eyes were grafted into embryos younger than stage 28. Control experiments confirmed the general correlation between the time of specification and the stage of the eye primordium. We infer that intraocular regulatory mechanisms control the time of specification.

Animals↗

Neuronal locus specificity: altered pattern of spatial deployment in fused fragments of embryonic xenopus eyes.

Before optic nerve outgrowth in Xenopus laevis embryos, a change of state occurs in the differentiating retinal cell population which renders the cells refractory to information about subsequent changes in their positions, and commits individual ganglion cells to develop specific position-dependent properties (locus specificities) which subserve the formation of orderly retinotopic connections in the optic tectum. When different parts of eye primordia from stages before optic nerve outgrowth are fused, each piece in such a reconstructed eye does not generate ganglion cells with the partial-set of locus specificities normally arising from that region of the intact eye. It is inferred that separate parts of the early embryonic retina do not contain stable programs for spatial deployment of locus specificity, and that development of definitive locus specificities in retinal ganglion cells requires additional cellular interactions among the retinal cells later in development.

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