Histology of the trachea and lung of Siphonops annulatus (Amphibia, Gymnophiona).

The structure of the trachea and lung of Siphonops annulatus was studied in ten specimens of routinely fed animals. The trachea is constituted mainly by incomplete cartilage rings lined by a respiratory epithelium (ciliated and mucous cells) with variable morphology according to the region observed. A rich vascularization of this organ suggests its participation in blood-air gas exchange. The right lung in this species is developed and the left one is atrophied. This organ is constituted mainly by longitudinal septa formed by connective tissue, smooth muscle cells and blood capillaries. These structures are covered by pneumocytes of one type only, which present cytoplasmic particles that have been related with surfactant activity described in the lung of Gymnophiona.

Histology of the kidney and urinary bladder of Siphonops annulatus (Amphibia-Gymnophiona).

The histology of the kidney and urinary bladder of Siphonops annulatus was studied by light microscopy in semithin sections of tissue embedded in hydrophilic resin. The kidney's nephron comprises the renal corpuscle, neck segment, proximal tubule, intermediate segment, distal tubule and collecting tubule. Nephrostomes are present. This structure, the neck segment, and intermediate tubules present long cilia, and probably play important roles in the propulsion of the peritoneal fluid and glomerular filtrate. The proximal tubule cells possess loosely packed microvilli and contain abundant polymorphic granules and vesicles that assume the aspect of lysosomes in different stages of intracellular digestion. The distal tubules are characterized by large, vertically disposed mitochondria assuming the aspect of ions transporting cells. The urinary bladder is lined with a transitional epithelium, whose aspect varies according to the quantity of urine.

Regeneration of fin rays in teleosts: a histochemical, radioautographic, and ultrastructural study.

Regeneration followed partial amputation of the tail fin in three representative species of teleosts. A systematic study, using histochemical methods, radioautography and transmission electron microscopy, disclosed the essentials of the natural history of regeneration of the fin soft-rays. At about 24 hours, epidermal cells had completely covered the cut edge. By the second day an apical epidermal cap was established. Beneath this cap a blastema was formed by about three days after amputation. A collagenous lepidotrichial matrix had begun to develop by 4 days after excision. Actinotrichia were first detected in the regenerates at 5 days. During these processes, the basal lamina of the epidermis played an important morphogenetic role. The cells responsible for the regenerate underwent regressive changes after form and function had been restored.

Epidermal glands in squamata: Fine structure of pre-cloacal glands in Amphisbaena alba (Amphisbaenia, Amphisbaenidae).

The femoral or cloacal region in lizards and amphisbaenians displays epidermal glands; these are commonly used for purposes of systematics. In spite of being recognized as semiochemical sources (Maderson [1986] Plenum Press, pp. 13-25), their precise role remains uncertain. The glands of lizards are assumed to be principally associated with reproduction and the demarcation of territory. Their function in amphisbaenians remains unknown. The histology of these glands has only been described for lizards. There are no ultrastructural studies of glands of either type. This study concentrates on the fine morphology of the pre-cloacal glands in Amphisbaena alba using routine histological and ultrastructural techniques. The pre-cloacal glands of amphisbaenians are, like those of lizards (Chiu and Maderson [1975] J. Morphol. 147:23-40), made up by a layer of germinative cells and various layers of polyhedral cells. The latter display three well-characterized stages of differentiation. Granules form and pass through two distinct stages. Thereafter, the granules fuse in the third stage. The glandular secretion is formed by cellular units that constitute the plug. Comparison of these morphological data with those available for lizards allows speculation about the function of the glands in amphisbaenians. © 1994 Wiley-Liss, Inc.

Diversity of collagen expression in the pleomorphic adenoma of the parotid gland.

The high diversity of collagen expression and its qualitative and quantitative aspects are demonstrated in pleomorphic adenoma using electron microscopy and specific histochemical methods. Great variability was observed in the amount, distribution and characteristics of the collagen found in the various types of tissue normally present in this tumour. Both deficient polymerization and hyperpolymerization of collagen and the occurrence of desmoplasia were observed. Evidence is presented to suggest a role for localized collagenolysis in the invasiveness of this neoplasia.

A simple procedure to obtain one-micrometer sections of routinely embedded paraffin material.

By freezing blocks of paraffin-embedded tissues to a convenient temperature it is possible to obtain routinely 1 micron sections that can be further processed as normal thicker sections. Normal and disposable steel knives can be used and the staining time should be increased in most procedures. Gradual freezing of blocks to the temperature of dry ice is the simplest and safest way to obtain an adequate temperature. The best results were obtained using as fixative 4% paraformaldehyde in phosphate buffered saline solution.

Morphologic evidence that disruption of the Golgi apparatus in PFHR 9-tumor cells causes disturbance in the traffic through this organelle.

PFHR 9 is a murine teratocarcinoma-derived tumor which produces basement membrane components. Electron microscopy of the tumor cells disclosed a disorganization of the Golgi complex whose saccules, instead of being flattened, round up into 0.13 micron-wide spherical vesicles (SV). Their shape does not permit the normal stacking of parallel cisternae, and thus these SV become intermingled with transport vesicles (TV) which measure 44 nm in diameter. The cytoplasm of these tumor cells contains numerous multivesicular bodies (MVB) of varying size (ranging from 0.3 to 2.6 micron), which occupy 7% of the cellular volume. These MBV are packed with very many small vesicles similar in all aspects to the TV, and also contain a few larger vesicles which resemble the altered Golgi saccules (SV). Since these MVB display morphologic evidence for gradual lysis of their contents and strongly react with the cytochemical method for acid phosphatase, it is assumed that MVB are autophagic vacuoles which result from the accumulation of TV. This seems to be a unique example of a disease of the Golgi stack, with consequent accumulation and disposal of this material via autophagic vacuoles.

A note on the histochemical and morphological characterization of the asbestoid degeneration of cartilage.

Using only one histologic preparation and under the light microscope, the simple Picrosirius-polarization method permitted the histochemical characterization of the collagenous nature of amianthoid fibers in file cases of salivary gland tumors. In this regard the foregoing results agree with the electron microscopic and X-ray diffraction observations recorded in the literature. Not only did the Picrosirius-polarization method permit the precise characterization of the collagenous nature of asbestoid change but it was also useful for studying the degree of collagen polymerization in the lesion. Collagen molecules in the amianthoid fibers showed hyperpolymerization whereas the molecules in the compact areas were disoriented. Since the foregoing results demonstrate that the Picrosirius-polarization method is a simple and sensitive procedure for detecting asbestoid change in cartilage sections obtained from paraffin-embedded tissues, the usefulness of this technique for studying file cases is evident.

Biology of metastasis.

1. Metastasis, i.e., dissemination of tumor cells throughout the organism, is the cause of death for most cancer patients. We discuss here the role of the interaction between basement membrane laminin and specific cell receptors in the process. We further show that such interaction is mediated by receptors not only in cancer cells but also in normal granulocytes, in a parasitic protozoan and even in an invasive prokaryote. 2. Metastatic potential has been correlated with the number of receptors/cell and preliminary results with a monoclonal antibody against the S. aureus laminin receptor suggest that the binding site at the receptor level might be conserved. This conclusion is supported by the facts that this monoclonal antibody can recognize the eukaryotic receptor and inhibit laminin binding.

A morphologic and histochemical study of the mesentery in the guinea pig.

The guinea pig mesentery is a uniform, continuous, thin (18 micron) sheet of connective tissue covered by a single layer of flattened mesothelial cells on both surfaces. Tight and gap junctions provide for cell-to-cell adhesion among mesothelial cells. These cells possess numerous micropinocytotic vesicles; a conspicuous basal lamina separates the mesothelium from the underlying connective tissue. Most of the material found between the two serous coverings consisted of a three-dimensional meshwork of abundant collagenous fibers intermingled with a sparse net of very thin (0.4 micron) elastic fibers. Two distinct populations of collagen fibrils are segregated into different compartments of the mesentery. One population is formed of thick (56 nm) fibrils which associate to form closely packed fibers. The second population, composed of loosely arranged thin (38 nm) fibrils which do not become assembled into fibers, is found underlying the basal lamina that separates the mesothelium from the connective tissue. These observations strongly suggest that the mesentery contains both collagens type I and type III. The guinea pig mesentery contains 6.8 mg of sulfated glycosaminoglycans/g dry weight. Most of these glycosaminoglycans (78%) were identified as dermatan sulfate, whilst the rest (22%) corresponded to heparan sulfate.