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Biomedical subjects

R D Fink

Publications and source records attributed to R D Fink.

16 recordsLinked to original sources

On the convergent cell movements of gastrulation in Fundulus.

Mainly because of its transparency, the Fundulus gastrula constitutes ideal material for direct study of morphogenetic cell movements in vivo. Marking studies show that deep cells of the germ ring converge toward and enter the embryonic shield, where they undergo extension. Those close to the shield move faster. Analysis of videotapes reveals that all deep cells of the dorsal germ ring move toward the shield. But none moves in a direct line. All meander considerably. Germ ring cells nearer the shield move toward it at a higher net rate than those farther away because they meander less. This suggests that exogenous factors promote their directionality. Cells in the prospective yolk sac adjacent to the germ ring also show net convergence, but they meander more. Directional forces are apparently stronger in the germ ring. Converging deep cells move both by filolamellipodia and, less frequently, by blebs. However, there is very little individual cell movement; all cells are almost always in adhesive contact with other cells in moving cell clusters. Clusters vary constantly in size, continually aggregating with other cells and other clusters and splitting. Filolamellipodial cells show contact inhibition of cell movement. Nevertheless, they move and do so directionally, presumably in part because, as members of cell clusters, much of their movement is passive. They also show intercalation or invasive activity, but, consistent with their contact-inhibiting properties, only when neighboring cells separate and provide free space. Cells moving by blebbing locomotion are non-contact inhibiting and intercalate readily. Cell division continues during convergence. Although this temporarily arrests their movement, the daughter cells soon join in the mass convergent movement.

Animals

Fundulus deep cells: directional migration in response to epithelial wounding.

During the normal embryogenesis of the killifish Fundulus heteroclitus deep cells migrate in an apparently random fashion throughout the subepithelial space of the yolk sac. These cells migrate by blebbing locomotion, and individual cells show tendencies for persistence in the directionality of their movement. Immediately after the wounding of the yolk sac epithelium (the enveloping layer), these deep cells reorient and migrate directionally toward the site of wound closure. This directional migration results in the aggregation of a large number of cells at the wound site. The response is both rapid and widespread; cells as far away as 800 micron respond as quickly as those nearby, and by 100 min after wounding up to 90% of the blebbing deep cells within this radius have clustered about the wound site. Then, cells begin to disperse, and by 150 min after wounding, it is almost impossible to tell where the wound had been made. Because of the transparency of the Fundulus yolk sac, this phenomenon can be utilized as a model system for observing details of in vivo directional cell movements. Time-lapse video micrography has revealed that the modes, rates, and overall cell morphologies during locomotion are identical for cells migrating in both unwounded and wounded embryos. What is different in the wounded embryos is that a single directionality is imposed upon a large population of cells, resulting in aggregation. Several aspects of the aggregation phenomenon suggest that a possible attractant originating at the wound site may travel through the subepithelial space by diffusion.

Animals

Three cell recognition changes accompany the ingression of sea urchin primary mesenchyme cells.

At gastrulation the primary mesenchyme cells of sea urchin embryos lose contact with the extracellular hyaline layer and with neighboring blastomeres as they pass through the basal lamina and enter the blastocoel. This delamination process was examined using a cell-binding assay to follow changes in affinities between mesenchyme cells and their three substrates: hyalin, early gastrula cells, and basal lamina. Sixteen-cell-stage micromeres (the precursors of primary mesenchyme cells), and mesenchyme cells obtained from mesenchyme-blastula-stage embryos were used in conjunction with micromeres raised in culture to intermediate ages. The micromeres exhibited an affinity for hyalin, but the affinity was lost at the time of mesenchyme ingression in vivo. Similarly, micromeres had an affinity for monolayers of gastrula cells but the older mesenchyme cells lost much of their cell-to-cell affinity. Presumptive ectoderm and endoderm cells tested against the gastrula monolayers showed no decrease in binding over the same time interval. When micromeres and primary mesenchyme cells were tested against basal lamina preparations, there was an increase in affinity that was associated with developmental time. Presumptive ectoderm and endoderm cells showed no change in affinity over the same interval. Binding measurements using isolated basal laminar components identified fibronectin as one molecule for which the wandering primary mesenchyme cells acquired a specific affinity. The data indicate that as the presumptive mesenchyme cells leave the vegetal plate of the embryo they lose affinities for hyalin and for neighboring cells, and gain an affinity for fibronectin associated with the basal lamina and extracellular matrix that lines the blastocoel.

Animals

The subacute phase of alcoholism.

Aggressive intervention in the medical and psychosocial problems of the subacute phase of alcoholism allows the physician to assume a holistic approach to the alcohol-addicted individual and provides a basis for eventual arrest of the chronic disease. A variety of metabolic abnormalities and physiologic disorders require attention. Management of psychologic problems requires the use of rational authority, early psychotherapy, judicious short-term psychopharmacology and use of available community resources.

Acute Disease