Katsuji Kaneko

Unilateral anomalous left common carotid artery; a case report.

An anomaly of the left common carotid artery was observed in a Japanese male cadaver during an anatomy class at the Saitama Medical School in 1995. The superior thyroid, lingual and facial arteries arose from the common carotid artery, and the posterior auricular, maxillary and superficial temporal arteries arose from the common carotid artery by a common trunk. The occipital and ascending pharyngeal arteries arose from the internal carotid artery. The left carotid body (glomus caroticum) was observed to be slightly below the lingual artery, behind the common carotid artery, and it was located at the level of the intervertebral disk between C2 and C3 or at the same level as the right carotid body. The carotid body was richly innervated by a branch of the glossopharyngeal nerve and by a plexus of sympathetic fibers from the vagus and glossopharyngeal nerves. We assumed that the artery above the level of the carotid body was the internal carotid artery; there was no specific external carotid artery and all branches of the external carotid artery arose from the internal carotid artery.

ROLES OF MACROPHAGES IN PROGRAMMED CELL DEATH AND REMODELING OF TAIL AND BODY MUSCLE OF XENOPUS LAEVIS DURING METAMORPHOSIS

Abstract Examination was made of the involvement of macrophage phagocytosis in programmed cell death of tail and body muscle of the frog, Xenopus laevis, during metamorphosis by electron microscopy and immunohistochemical analysis. Electron microscopic observation revealed that macrophages were often found to be present in body and tail muscles at the most active stage of metamorphosis and to actively phagocytose apoptotic muscle fragments. Developmental changes in macrophages were examined using the macrophage-specific antibody, HAM56. Macrophages initially appeared in the early climax stage (stage 59), when the triiodothyronine (T3) level was high, increased rapidly during the process of muscle cell death, and assumed their greatest number at the late climax stage (stage 63/64). They decreased after stage 65/66, with a decrease in T3. Distribution and change in the number of macrophages were the same as those of muscle apoptotic bodies (sarcolytes) during metamorphosis, which suggests an interactive mechanism between macrophages and dying muscle cells. For clarification of this, study was made of the expression of HAM 56 antigens that were X. laevis homologs of mouse attachmin, non-specific adhesion proteins in macrophages. The expression of HAM56 antigens in macrophages was found to increase with macrophage phagocytosis at the late climax stage, thus, macrophage differentiation would appear to take place during metamorphosis and HAM56 antigens may be essential for macrophage–dying muscle cell interactions.

Formation of new capillary-like tubes in a three-dimensional in vitro model (aorta/collagen gel).

Direct sprouting (angiogenesis) does not occur during the formation of capillary-like tubes in an aorta/ collagen gel in the in vitro model. However, emigration of cells which stretch, arrange themselves side by side, form contacts (unspecific, tight and gap junctions), develop a lumen and show differentiation of endothelial cells (including the formation of a lamina densa and the appearance of pericytes) have been observed, i.e. vasculogenesis occurs. The origin of long, stretched cells is not known with certainty. They possibly represent smooth muscle cells. In addition, other cell types have been found, such as fibrocyte-like and fibroblast-like cells, elastoblasts, fat cells, monocytes and macrophages. All these cells are able to produce factors that promote the formation of new capillaries. Hence, a knowledge of these cells appears to be important for the analysis of in vitro systems. Moreover, the occurrence of these cell types must be considered when assessing possible effects.

Cell shape and arrangement of cultured aortic smooth muscle cells grown on collagen gels

Aortic smooth muscle cells (SMC) grown on conventional plastic culture dishes have morphological and functional properties of dedifferentiated cells in sub-culture. We examined the influence of collagen gels on the cell shape and arrangement. The cells grown on collagen gels showed a multilayered growth with formation of nodules. When the edge of the collagen gels was detached from the culture dish, the shape and arrangement of cells on the edge differed from that of the central, still attached region. The cells grown on floating collagen gels exhibited a spindle-like shape and were arranged in concentric circles. These findings suggest that the physical property of the substrate influences the cell shape and arrangement.

Morphology of capillary-like structures in a three-dimensional aorta/collagen gel culture

The morphology of capillary-like tubes was investigated by electron microscopy (TEM and SEM) using an in vitro model of capillarogenesis (aorta/collagen type I gel). This model allowed morphological comparisons with in vivo capillaries and an evaluation of the functional maturity of the endothelium to be made. The lumina developing in vitro were demarcated by endothelial cells of varying thickness (0.1-2 microns). Pericytes were resting on the outside. The endothelial cells were characterized by contacts of varying length with tight and gap junctions and occasional indentations. The inner surface exhibited areas both with pronounced and without any endocytotic activity. In addition to a large Golgi apparatus, a varying number of cell organelles occurred depending on the thickness of the endothelium. Bundles consisting of microfilaments were often located underneath the outer cell membrane and in the vicinity of contact areas. A lamina densa was in the process of formation. The capillaries grown in vitro closely resembled those in vivo and showed a high degree of differentiation. Hence, this in vitro model allows the study of a number of functions of endothelial cells.

Changes Associated with the Basal Lamina during Metamorphosis of Xenopus laevis

We examined the changes in the morphology of the basal lamina of the colon, abdominal wall and tail muscles of tadpoles during metamorphosis and compared our results to those previously obtained for the small intestine. At the early stage of metamorphic climax (stages 60-62), we observed a curving of the basal lamina along the processes of the epithelial cells. At a later stage of metamorphic climax (stages 63-66), more extensive curving and folding of the basal lamina were observed. The basal lamina of the mesothelial cells in the abdominal wall did not change extensively as compared to the colon. Folded basal lamina was observed among degenerated muscle cells. Our results suggest that the folding of the basal lamina depends on the degree of deformation of the particular organ, which occurs mainly by physical factors such as the shortening or shrinking of the organ due to cellular degeneration. Cells that are newly differentiated produce an additional basal lamina, which results in transient doubling or layering. The combination of physical factors and cell differentiation results in a basal lamina that is more complex and contains folds and layers.

Basement Membrane Formation of Fetal Mouse Intestinal Epithelial Cells in Organoid Cultures

Basement membrane formation of fetal mouse intestinal epithelial cells was investigated in organoid cultures. Intestinal cells were dissociated with a commercial collagenase/dispase preparation, and the cells were grown at high density on a membrane filter at the interface between the medium and air. This type of culture allows the histotypical reorganization of cells. After 2 days in culture, epithelial cells began to accumulate on the surface, in particular the periphery of the culture. These cells were usually cuboid, and small vesicles were formed in the center of the culture. Laminin-positive material was observed at peripheral sites. However, no basement membrane could be identified beneath the epithelial cells at the electron-microscopic level. After 3 days, epithelial cells that had gathered at the periphery became columnar in shape. Laminin-positive material extended across the surface of the culture. However, the vesicles formed in the center of the culture were not associated with laminin-positive material. Basement membrane was observed by electron microscopy at some sites beneath groups of epithelial cells, but did not extend continuously beneath these cells. Some epithelial cells made contact with the underlying mesenchymal cells through the discontinuous basement membrane via intercellular contacts. After 5-6 days, the surface of the culture was almost completely covered with epithelial cells and, at some sites, villus-like structures were visible. Laminin-positive material was clearly detectable under epithelial cells, as well as around epithelial vesicles located in the center of the culture. By electron microscopy, basement membrane was clearly visible between the epithelial and mesenchymal cells. After 9 days, villus-like structures were rarely observed. After 3 weeks, the cell mass had become smaller and villi had disappeared. Basement membrane was extensively folded and no basement membrane was visible at some sites. Formation of basement membrane by epithelial cells in monolayer culture occurs in an incomplete and irregular manner. It occurs rapidly in organoid cultures that include mesenchyme and epithelium. The organoid culture used here should be a useful tool for studies of the formation and degeneration of the basement membrane as well as interactions between the epithelium and mesenchyme.

Immuno-electron-microscopic application of antiserum against elastin

The antiserum against insoluble elastin from human aorta was applied to immuno-electron microscopy. In the preembedding method, only the outer surface of the amorphous component (elastin) of elastic fibers showed a positive reaction. A major problem encountered with the preembedding method is associated with the penetration of either the primary antiserum or the secondary antibody into the tissue and, in particular, into elastin. On the contrary, a positive reaction was observed inner zones of elastin in the postembedding method. While the postembedding method employed here has limitations with nonspecific binding to the embedding medium, the postembedding method offers a decided advantage over the preembedding method.

A New Method Using a Modified Mayer's Hemalum at pH 6 for Demonstrating Mucous Neck Cells

The mucous neck cells of gastric glands were stained with a modified Mayers hemalum adjusted to pH 6 with saturated aqueous lithium carbonate. One gram of hematoxylin was dissolved in 1000 ml distilled water and 200 mg sodium iodate, 3 g potassium alum, 50 g chloral hydrate and 1 g citric acid were added to the solution. Prior to staining, the solution was adjusted to pH 6 with saturated aqueous lithium carbonate. Bromine oxidation and urea abolished the alum hematoxylin reactivity of the mucous neck cells.