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J B Bard

Publications and source records attributed to J B Bard.

50 records · Page 3Linked to original sources
PubMed1979

Epithelial-fibroblastic organization in cultures grown from human embryonic kidney: its significance for morphogenesis in vivo.

The morphological behaviour of explants of human embryonic kidney has been studied in order to investigate the rules governing interactions between epithelial and fibroblastic cells from the same tissue. When the fragments are cultured, epithelia migrate out first and are followed, a few days later, by cables which grow out from the fragments and which are composed of multilayered fibroblasts. These cables extend through the epithelia to reach the substratum, to which they adhere. The epithelia maintain an upper surface free of spread fibroblasts and are unable to multilayer, although occasional rounded-up cells adhere to this surface. Fibroblasts, however, not only multilayer in the cables but can act as a substratum for epithelial cells which migrate on the cable surface. Fibroblasts and epithelia from kidney thus follow the same behavioural rules that govern the interactions between kidney epithelia and fibroblasts from different tissues. The suggestion that these rules derive from tissue differences and that cells from the same tissue are more tolerant of one another is not borne out. These observations and those reported by others are interpreted in terms of the functional properties of the cells in vivo. It is further pointed out that only those epithelia that maintain a free surface in vivo would be expected to show this property in vitro. Finally, the implications of cells with essentially the same properties generating more than one structure are considered.

Cell Adhesion↗
PubMed1977

Fibroblast-collagen interactions in the formation of the secondary stroma of the chick cornea.

Fibroblasts invade the primary corneal stroma of the 6-day-old chick embryo eye. The way in which these cells build the secondary stroma has been studied by microscope examination of the stroma during the subsequent 8 Days. Eyes were embedded in low viscosity nitrocellulose, and 30-micrometer tangential sections of cornea were cut and stained with azan (giving blue collagen and red cells). These sections were sufficiently thick to include enough cells and collagen for stromal organization to be visible under Nomarski optics. Three days after invasion, the fibroblasts extend along collagen bundles in the posterior region of the stroma; surprisingly, fibroblasts near the epithelium are more rounded. The collagen itself is organized in orthogonal bundles rather than in sheets. Measurements show that posterior bundles increase in size with time while anterior stroma si similar in diameter to primary stroma. These observations confirm that the epithelium continues to deposit primary stroma up to at least the 14th day. They show, moreover, that fibroblasts deposit collagen fibrils on extant stroma and that the farther a bundle is from the epithelium, and hence the longer the period since it was first laid down, the wider it is likely to be. Analysis of the results and existing data on hyaluronic acid levels in the stroma suggests that Bowman's membrane, the region of anterior stroma that remains uncolonized by cells, is, during this period at least, primary stroma laid down but as yet unswollen.

Animals↗
PubMed1975

The behavior of fibroblasts from the developing avian cornea. Morphology and movement in situ and in vitro.

The early chick cornea is composed of an acellular collagenous stroma lined with an anterior epithelium and a posterior endothelium. At stage 27-28 of development (5 1/2 days), this stroma swells so that the cornea is 75-120 mum thick. At the same time, fibroblasts that originate from the neural crest begin to invade this stroma. Using Nomarski light microscopy, we have compared the behavior of moving cells in isolated corneas with the migratory activities of the same cells in artificial collagen lattices and on glass. In situ, fibroblasts have cyclindrical bodies from which extend several thick pseudopodia and/or finer filopodia. Movement is accompanied by activity in these cytoplasmic processes. The flat ruffling lamelli-podia that characterize these cells on glass are not seen in situ, but the general mechanism of cell movement seems to be the same as that observed in vitro: either gross contraction or recoil of the cell body (now pear shaped) into the forward cell process, or more subtle "flowing" of cytoplasm into the forward cell process without immediate loss of the trailing cell process. We filmed collisions between cells in situ and in three-dimensional collagen lattices. These fibroblasts show, in their pair-wise collisions, the classical contact inhibition of movement (CIM) exhibited in vitro even though they lack ruffled borders. On glass these cells multi-layer, showing that, while CIM affects cell movement, fibroblasts can use one another as a substratum. Postmitotic cells show CIM in moving away from each other. Interestingly, dividing cells in situ do not exhibit surface blebbing, but do extend filopodia at telophase. The role of CIM in controlling cell movement in vivo and in vitro is stressed in the discussion.

Animals↗
PubMedDate not supplied

Importance of vitamin C in maintenance of the normal amnion: an experimental study.

Collagenous matrix in amnion accounts for most of the dry weight of the tissue and provides its mechanical strength and resistance to rupture. Cell and organ culture techniques have been utilized to study the influence of vitamin C upon the synthesis and deposition of extracellular matrix by cells of normal amnion at term. The cultures have been examined using light and electron microscopy and metabolic labelling. These studies show that both epithelial cells and fibroblasts of the deeper stromal layer are active in the production of fibrillar matrix at this time. Matrix deposition by epithelial cells in culture increases several-fold when the vitamin C concentration in the supernatant medium is increased from zero to 50 micrograms/ml, and, at the latter concentration, a continuous anastomosing fibrillar collagenous meshwork appears beneath the cells. This study thus provides new evidence that an adequate dietary supply of vitamin C is probably needed to maintain the strength of the chorioamnion.

Amnion↗
PubMedDate not supplied

Embryonic kidney rudiments grown in adult mice fail to mimic the Wilms' phenotype, but show strain-specific morphogenesis.

12.5- to 14.5-day mouse embryonic kidney fragments were grown syngeneically under kidney or testis capsules in 3 mouse strains for 5-26 weeks to reproduce the Wilms' tumour (WT) phenotype previously reported. About 65% of the transplants grew, but none showed true WT morphology, invaded local tissue or developed metastases. In Swiss mice, most growths contained disorganized stromal and blast cells, but also had more mature structures. CBA growths had cysts, differentiated nephrons and glomeruli, while 129/SV growths gave both types of morphology. In situ mRNA hybridization using the Wilms' tumour predisposition gene (WT1) showed that, unlike the initial rudiments and WT, expression was limited to the glomeruli. The unexpected absence of expression by the apparent blast cells in the growths implies that the system is not a model for WT.

Animals↗