The elastic system of normal human skin was studied by light and electron microscopy. By light microscopy three different types of fibers were observed: oxytalan, elaunin, and elastic. The most superficial ones (oxytalan fibers) are very thin and directed perpendicularly to the dermoepidermal junction. They start from a plexus with the tinctorial characteristics of elaunin fibers which is connected with the thicker elastic fibers of the reticular dermis. At the electron microscopic level the oxytalan fibers are formed by bundles of tubular microfibrils 10 to 12 nm in diameter. In the deepest layers of the dermis an amorphous material is seen in the core of these bundles. In the elaunin fibers the amorphous material is sparse, while in the elastic fibers it is abundant and compact.
Fixation with tannic acid-glutaraldehyde permits distinction of oxytalan, elaunin and elastic fibers in the electron microscope. The results obtained using tannic acid at concentrations of 1.0%, 0.5% and 0.25% in 3% glutaraldehyde were compared. The 0.25% concentration is recommended for studying fine details of connective fibrils and for regular staining of elastin.
Morphologic and biochemical studies were performed on cultures of bovine aortic endothelial cells which had developed a second growth pattern that has been referred to as "sprouting" (Gospodarowicz and Mecher, '78; Schwartz '78). These morphologically atypical cells undergrew the intact endothelial cell monolayer and appeared only after the cells had reached confluence. They were ultrastructurally very similar to endothelial cells, but synthesized reduced amounts of fibronectin and a predominance of type I procollagen, rather than the types III and IV procollagens synthesized by monolayer endothelial cells. It is suggested that these cells represent phenotypically altered endothelial cells that differ in biosynthesis of secreted proteins and display a reduced contact-inhibition.
Rat hyaline and fibrous cartilages whose glycosaminoglycans had been removed by hyaluronidase digestion were studied by comparing the ultrastructural features with the observation of sections stained by selective methods for elastic system fibers under the light microscope. Except for the fibrous layer in the perichondrium of tracheal hyaline cartilage, where elastic fibers were found, no elastic fibers could be detected in the cartilages studied. However, cartilaginous tissues contained oxytalan and elaunin fibers. A distinct pattern of distribution of the above-mentioned elastic-related fibers could be observed in both kinds of cartilages. Hyaline cartilages possess oxytalan fibers in the extracellular matrix that surrounds the chondrocytes, whereas elastic fibers were localized in the fibrous layer of the perichondrium that encloses the cartilage. Elaunin fibers could be detected in the transition (chondrogenic) layer adjacent to the perichondrium. The methods used disclosed the presence of oxytalan and elaunin fibers running along the periphery of the collagen bundles in fibrocartilage.
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