Role of cell adhesion in contact-dependent transfer of a lysosomal enzyme from lymphocytes to fibroblasts

1986 ◽  
Vol 85 (1) ◽  
pp. 231-244
Author(s):  
I. Olsen ◽  
T. Oliver ◽  
H. Muir ◽  
R. Smith ◽  
T. Partridge

Normal lymphocytes were found to adhere strongly to monolayer cultures of fibroblasts deficient in the lysosomal enzyme, beta-glucuronidase. During this co-culture, the fibroblasts acquired from the lymphocytes substantial amounts of this enzyme, which often accumulated at sites of contact between the two types of cell. Enzyme transfer was prevented by addition to the co-cultures either of purified lymphocyte plasma membranes or of antibody raised against such plasma membranes, but it was not inhibited by the addition of antibody raised against lymphocyte-derived beta-glucuronidase. An active role for the lymphocyte in this contact-dependent process was suggested by interference contrast, immunofluorescence and scanning electron-microscopic studies. These revealed extensive arrays of projections of the lymphocyte that ramified over the fibroblast cell surface. By transmission electron microscopy, conspicuous clusters of micropinocytotic vesicles were evident in the cytoplasm of the ‘recipient’ fibroblasts, subjacent to the surface in regions closely apposed to adherent lymphocytes. Such high frequencies of these vesicles were restricted to sites of lymphocyte-fibroblast contact, suggesting that they may play an important part in the transfer of enzyme between these two types of cell.

Author(s):  
Grace C.H. Yang

The size and organization of collagen fibrils in the extracellular matrix is an important determinant of tissue structure and function. The synthesis and deposition of collagen involves multiple steps which begin within the cell and continue in the extracellular space. High-voltage electron microscopic studies of the chick embryo cornea and tendon suggested that the extracellular space is compartmentalized by the fibroblasts for the regulation of collagen fibril, bundle, and tissue specific macroaggregate formation. The purpose of this study is to gather direct evidence regarding the association of the fibroblast cell surface with newly formed collagen fibrils, and to define the role of the fibroblast in the control and the precise positioning of collagen fibrils, bundles, and macroaggregates during chick tendon development.


Author(s):  
T. B. Cole ◽  
D. T. John

Naegleria fowleri is an opportunistic free-living amoeboflagellate that is the causative agent of the rapidly fatal disease in man called primary amoebic meningoencephalitis. This pathogenic amoeba displays surface sucker-like structures called amoebostomes that have been shown to play an active role in a unique form of engulfment. Transmission electron microscopic studies of amoebostome profiles demonstrate associated cytoskeletal components. It is known that cytochalasin B (CCB) produces reversible alterations in the cell's cytoskeleton and in turn modification of surface characteristics. Therefore, the purpose of this study is to observe the morphological effects that CCB has on amoebostome morphology.


1986 ◽  
Vol 95 (4) ◽  
pp. 409-414 ◽  
Author(s):  
Phillip A. Wackym ◽  
Ulla Friberg ◽  
Dan Bagger-Sjöbäck ◽  
Helge Rask-Andersen

The ultrastructure of the normal human endolymphatic duct (ED) was observed by transmission electron microscopy. The role of the epithelium, the various regions of the subepithelial space, and vasculature in the resorption of endolymph was morphologically studied in order to generate testable hypotheses of human ED function. These hypothetical mechanisms of endolymph outflow at the level of the ED are 1) a passive transcellular movement of water across the epithelium, driven by an osmotic gradient created by a subepithelial organic matrix; 2) an active transcellular ion exchange with a passive transepithelial outflow of water, which stresses the importance of the dilated lateral intercellular spaces; and 3) an active transcellular vacuolar endolymph outflow, whereby high molecular weight substances are removed by the ED. These mechanisms may be useful in designing experimental studies of the ED and in interpretation of retrospective light microscopic and transmission electron microscopic studies of patients with Meniere's disease.


Author(s):  
M.G. Hamilton ◽  
T.T. Herskovits ◽  
J.S. Wall

The hemocyanins of molluscs are aggregates of a cylindrical decameric subparticle that assembles into di-, tri-, tetra-, penta-, and larger multi-decameric particles with masses that are multiples of the 4.4 Md decamer. Electron micrographs of these hemocyanins typically show the particles with two profiles: circular representing the cylinder viewed from the end and rectangular representing the side-view of the hollow cylinder.The model proposed by Mellema and Klug from image analysis of a didecameric hemocyanin with the two decamers facing one another with collar (closed) ends outward fits the appearance of side-views of the negatively-stained cylinders. These authors also suggested that there might be caps at the ends. In one of a series of transmission electron microscopic studies of molluscan hemocyanins, Siezen and Van Bruggen supported the Mellema-Klug model, but stated that they had never observed a cap component. With STEM we have tested the end cap hypothesis by direct mass measurements across the end-views of unstained particles.


RSC Advances ◽  
2016 ◽  
Vol 6 (48) ◽  
pp. 42334-42346 ◽  
Author(s):  
Suchitra Parija ◽  
Arup R. Bhattacharyya

Transmission electron microscopic image of separated MWCNTs (N51L15G5) showing the wrapped polymer chains on the MWCNTs surface, which corresponds to the α-phase of the PP.


Development ◽  
1974 ◽  
Vol 32 (1) ◽  
pp. 133-145
Author(s):  
Par Claude Chapron

Evidence for the role of an apical cap glycoprotein in amphibian regeneration: cytochemical and autoradiographic electron-microscopic studies Early during limb regeneration in the newt, an ectodermal apical cap covering a mesodermal blastema is formed. High-resolution autoradiography of these tissues has been carried out after incorporation of [3H]fucose, which is a precursor of glycoproteins. Autoradiography shows that silver particles are located at first on epithelial cells, then on mesenchymatous cells. This observation is consistent with a hypothesis in which the apical cap would elaborate a glycoprotein acting on the blastema. Substructural autoradiography and cytochemistry also show the importance of cellular surfaces for both cells producing glycoprotein and those which are target cells.


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