Zeitschrift fur mikroskopisch-anatomische Forschung最新文献

Ultrastructure and histochemistry of clinically normal appearing tissue and secretions of non-lactating human mammary glands have been investigated in order to document and analyse secretory phenomena in the resting gland. The material studied originated from women of different ages (18-74 years) who underwent plastic surgery or surgery for various disorders of the breast. The epithelia of small ducts and of alveolar enlargements as well as acini contained moderate amounts of mitochondria and of cisterns of the rough endoplasmic reticulum; the transcisterns of the Golgi apparatus which were surrounded by smooth and coated vesicles, exhibited modest dilatations, the number of lysosomes increased with age; regularly glycogen particles and bundles of intracellular filaments (phi 5 nm) were to be observed. Typical casein vesicles and stages of apocrine secretion of milk fat globules were not seen. The following features indicated secretory activity: differently sized vesicles and granules with flocculent, dense, or light contents were regularly to be seen in the apical cytoplasm often immediately below the apical plasma membrane of the epithelia of the small ducts and even more frequently in the alveolar enlargements. Secretory products of fine granular or filamentous structure, probably containing proteins, were frequently found within the lumen. Different types of lipid and liposome-like particles were detected both in intracellular localization as well as in ductal lumina. As demonstrated by lectin histochemistry the secretory products also contained a considerable amount of carbohydrate components. The composition of the secretory products of the resting gland is of clinical interest since the chronical deposition of secretions, which among others possibly contain enzymes producing oxygen radicals, may lead to pathological changes of mammary gland tissue.

The myenteric plexus of the domestic fowl (Gallus domesticus) small intestine was studied by means of silver staining, glyoxylic acid-induced fluorescence, the modified Koelle-Friedenwald method for the detection of acetylcholinesterase, NADH-diaphorase techniques and the unlabelled antibody method involving the use of an antiserum raised against GABA conjugated by glutaraldehyde to bovine serum albumin. The majority of the perikarya were in the ganglia, with an average density of 3370 +/- 942 nerve cells/cm2. Cholinesterase-positive and a few GABA-immunoreactive nerve cell bodies were seen in the myenteric ganglia, while fluorescent ganglion cells were not observed. In addition to AChE and GABA-positive nerve fibres, a rich fluorescent network of varicose and nonvaricose nerve fibres was detected, pointing to the presence of an extrinsic aminergic system in the domestic fowl myenteric plexus. Electron microscopic observations on nerve cells, axon profiles and varicosites with various vesicle populations were in good agreement with the histochemical findings.

Samples of cervical, mediastinal and perirenal fat tissue were obtained from eight subjects (ages: 17 days to 56 years) at necropsy. After formol fixation, the specimens were processed for sectioning and stained with hematoxylin and eosin, periodic acid--Schiff, or Holmes' silver techniques for light microscopy. All the tissue samples showed lobular organisation and a rich vascularity, with argentaffin (putative nerve) fibres at paravascular and parenchymal sites. Three histological forms of brown adipose tissue (BAT) were recognised: homogeneous lobules of multilocular adipocytes (Type I); mixed lobules consisting of islets of multilocular adipocytes surrounded by large unilocular cells (Type II); and lobules consisting mainly of small (less than 40 microns diameter) unilocular adipocytes (Type III). In two subjects (ages 17 days and 52 years), BAT (Types I and II respectively) was observed in tissue samples from all three sites. Perirenal samples from three other donors (ages 26-35 years) showed the presence of Type II or III BAT. Mediastinal BAT (Type II) was found in two subjects (26- and 35-years old). The significance of BAT in man inhabiting a warm environment is discussed.

This paper describes observations of the normal and irritatingly changed morphology of the human peritoneum and about alterations in human peritonitis. The results were obtained by transmission- and scanning electron microscopy, immunohistochemical reactions, and other supplementary light microscopic investigations on surgically collected tissue material. Special attention was given to the superficial structure and the openings of the peritoneum. The superficial liquid film and the microvilli of the mesothelium are influenced by irritative conditions. In the human peritoneum, there are separated areas of small high and of large flat mesothelial cells. The small-cell areas of the peritoneum are connected with openings, special mesothelial cell glades, and cell migrations from deeper parts. There are signs of mesothelial secretion into the peritoneal cavity from mesothelial cells and intercellular spaces of the mesothelium too. The stomata--openings of the peritoneum--are of conditioned character. These depends upon the state of the superficial mesothelium and upon topical loci between the mesothelial cells. Special attention requires the so-called Dreierpunkt. In peritonitis, there are also openings in the fibrin layer. On this condition, the superficial layer of mesothelium mostly becomes destroyed. The keratin reaction is the most essential among the immunohistochemical investigations. It allows to demonstrate preserved mesothelial cells in the deepness of inflammatory tissue in peritonitis.

A malignant tumour of the rat pancreas with features of both acinar and endocrine cells is presented. This consisted of a continuous cytoplasmic mass with numerous dispersed nuclei and branches protruding from its borders invading the surrounding exocrine tissue. The most prominent characteristic of the tumour was the co-existence of zymogen and endocrine secretory granules and cytoplasmic organelles typical of both acinar and islet cells. Some hypotheses are put forward concerning the origin of the tumour and its vasculature.

Maturing ovarian follicles undergoing atresia were ultrastructurally analyzed. Using the method of Okrös (1968) the process of luteinization was traced, taking place in the basal layer of cells of granulous membrane and in the cells of inner layer of theca interna during the atresia. In the atresia process, numerous electron dense granules arranged in packets and surrounded by tubular mitochondria are observed in the basal cell layer of granulous membrane. A considerable accumulation of the grains of reaction product and the presence of tubular mitochondria are also found in the cells of theca interna. Such a behaviour of those cells can be associated with an enhanced production of steroid hormones (mainly estrogens) in atretic follicles.

The described triple staining (PAP, aldehydefuchsin, and cresyl violet) enables the distinction of different neuronal types with regard to their content of neurotransmitters or neuropeptides and their lipofuscin pigmentation respectively. The use of filters improves the contrast of immunohistochemical and lipofuscin staining, and facilitates the differentiation of neurons under the microscope. An additional important point is the advantage that perikaria can be measured in the usual morphometric manner.

Ten lectin-binding patterns were examined with the PAP method for the detection of sugar residues on the Harderian glands of golden hamsters of both sexes. Each lectin showed a specific binding pattern. The most characteristic pattern was exhibited by DBA which intensely stained cells with small lipid vacuoles, but not cells with large lipid vacuoles in the male gland. In the female gland, both cell types showed no reaction with the DBA. The PNA had almost the opposite binding pattern. From the lectin-binding patterns, it can be derived that, not only do the two cell types in same sex glands have different glycoconjugate distribution, but also the same type of cells in different sex glands has a different glycoconjugate distribution. Therefore, the sexual dimorphism of the golden hamster Harderian gland also occurs in its carbohydrate moieties. In this study, the duct of the Harderian glands revealed no sexual dimorphism in the lectin-binding patterns.

Epon sections from glutaraldehyde-fixed rat bone marrow were treated with aqueous solutions of the following electron contrasting agents: uranyl acetate, ruthenium red, potassium permanganate, potassium dichromate, stannous chloride, palladium (II) chloride, sodium molybdate, phosphomolybdic acid, molybdenum heteropolyblue, phosphotungstic acid, iron(II)-phenanthroline, aluminium-hematoxylin, mercurochrome, cuprolinic blue, and sirius light turquoise blue. At the ultrastructural level, a high degree of electron opacity was always observed in mast cell granules and the crystalline inclusion (internum) of eosinophil granules. The chromatin revealed a somewhat lower and variable contrasting reaction, while the matrix (externum) of eosinophil granules appeared with scarce or no contrast. This pattern of electron opacity showed no correlation with the type of agent used; therefore, it can be assumed that binding processes based on the own chemical reactivity of the compounds are rather of secondary importance. The differential epoxy resin embedding of cell structures and the variable access of aqueous reagents through the non-polar plastic could be the predominant factors which account for these contrasting reactions.

The presence of some cytoskeletal proteins related to the intermediate filaments glial fibrillary acidic protein -GFAP and vimentin) and S-100 protein has been investigated in sensory formations of the glabrous skin of the rat. A positive reaction both for S-100 protein and vimentin was found in the inner core and related cells of glomerular and simple sensory corpuscles; in contrast, no positive reaction was shown for GFAP. The authors discuss these results on the basis of the glial origin of the inner core and related cells in sensory formations.