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  • 1
    ISSN: 1432-0568
    Keywords: Articular cartilage ; Development ; Type I collagen ; In situ hybridization ; Immunohistochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The present study was designed to investigate whether or not chondrocytes in articular cartilage express type I collagen in vivo under physiological conditions. Expressions of the gene and the phenotype of type I collagen were examined in rat tibial articular cartilage in the knee joint during development. Knee joints of Wistar rats at 1, 5, and 11 weeks postnatal were fixed in 4% paraformaldehyde with or without 0.5% glutaraldehyde and decalcified in 10% EDTA. After the specimens were embedded in paraffin and serial sections made, adjacent sections were processed for immunohistochemistry and in situ hybridization for type I collagen. The epiphysis of the tibia was composed of cartilage in week-1 rats. Formation of articular cartilage was in progress in week 5 as endochondral ossification proceeded and was completed in week 11. Anti-type I collagen antibody stained only the superficial area of the epiphysis in week 1, but the immunoreactivity was expanded into the deeper region of the articular cartilage with development in weeks 5 and 11. Hybridization signals for pro-alpha 1 (I) collagen were seen in some of chondrocytes in the epiphysis of the week-1 tibia. The most intense signals were identified in chondrocytes in week 5 and the signals appeared weaker in week 11. The present study demonstrated that chondrocytes synthesize type I collagen and accumulate the protein in the matrix during development of the articular cartilage.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Virchows Archiv 385 (1980), S. 247-261 
    ISSN: 1432-2307
    Keywords: Myofibroblast ; Myoepithelial cell ; Human breast carcinoma ; Ultrastructural study
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Ultrastructural studies of 11 human breast carcinomata revealed that most stromal cells could be arranged in a cell spectrum from fibroblasts, with abundant rough endoplasmic reticulum, to myofibroblasts. In 4 out of 11 cases, myoepithelial cells were observed in the parenchyma at the periphery of some carcinomatous duct-like structures or carcinoma cell nests. The distinction between myofibroblasts and myoepithelial cells was usually easy from their respective locations. Their ultrastructural features were summarized as follows. Myofibroblasts: (1) abundance of rough ER and other cytoplasmic organelles; (2) bundles of microfilaments, 50–70 Å in diameter and associated dense bodies. Myoepithelial cells: (1) bundles of microfilaments 50–70 Å in diameter and associated dense bodies (a common feature); (2) dense bundles of tonofilaments, 80–100 Å in diameter; (3) typical desmosomes which connected them with adjacent myoepithelial or carcinoma cells. Myofibroblasts were occasionally located closely contiguous with carcinoma cells, giving an appearance resembling myoepithelial cells. Even in these instances a distinction between myofibroblasts and myoepithelial cells was possible, since myoepithelial cells had dense bundles of tonofilaments and typical desmosomes, which were not observed in myofibroblasts. No cell types intermediate between myofibroblasts and myoepithelial cells were detected. We could not decide whether myoepithelial cells were neoplastic or not despite the facts that they showed obscured polarity and had partially or completely lost their basal lamina. We conclude that fibroblasts, myofibroblasts and probably some, if not all, smooth muscle cells belong to the same cell system. Myofibroblasts in our material are derived from fibroblasts, while myoepithelial cells are epithelial in origin.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-2307
    Keywords: Inflammatory bowel disease ; ELAM-1 ; Endothelial cells ; Immunoelectron microscopy ; Neutrophils
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Endothelial leucocyte adhesion molecule-1 (ELAM-1) is a rapidly inducible adhesion molecule for neutrophils in vascular endothelial cells. We investigated its immunohistochemical localization in 17 cases of inflammatory bowel disease. ELAM-1 was preferentially expressed in venules in actively inflamed mucosa and granulation tissue. Most capillaries were negative for ELAM-1. In areas with mild inflammation its expression diminished markedly and in normal mucosa of the colon and small intestine its expression was sparse. Electron microscopically, venules in active inflammation had swollen endothelial cells with well-developed rough endoplasmic reticulum. Immunoelectron microscopy revealed ELAM-1 localization along the luminal plasma membrane and in rough endoplasmic reticulum and round granules, findings suggestive of active production in endothelial cells. Furthermore, exocytosis of immuno-reactive substance into the lumen was confirmed. Our study suggests that venules in actively inflamed area play an important role in eliciting and/or maintaining acute inflammatory processes by active permeation of neutrophils from the blood stream into the tissue, and that ELAM-1 may be a secretory protein as well as a transmembrane receptor protein.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-2307
    Keywords: Gastric carcinoma ; Capillaries ; von Willebrand factor ; Ultrastructure ; Immuno-electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The microvasculature of the stroma of human gastric carcinoma was studied by immuno-electron microscopy for factor VIII/von Willebrand factor (vWF) and conventional electron microscopy. In differentiated type (intestinal) gastric carcinoma (9 cases), capillaries were distributed more densely around carcinoma cell nests. vWF was localized in endothelial cells and neighbouring stroma. Ultrastructurally, capillary endothelial cells showed considerable hypertrophic changes with well-developed rough endoplasmic reticulum (rER). vWF was localized in well-developed rER, granules, Weibel-Palade bodies (WPB), in the vascular lumen as clusters, and diffusely deposited in the subendothelium. This indicates that endothelial cells in this group are transformed into a state of active protein production. In undifferentiated type (diffuse) gastric carcinoma (12 cases), capillaries were uniformly distributed and endothelial hypertrophic changes were less remarkable. vWF was localized in WPB, scanty rER and subendothelial matrix. Solid capillary buds were observed in both types; they were composed of a solid strand of endothelial cells without a visible lumen. Our results reveal that the microvasculature in tumour stroma differs significantly according to its histological type.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] In a search for new members of the GATA factor family, we analysed RNAs isolated from tissues of a 5-week-old mouse by blot hybridization analysis using a fragment encoding the zinc-finger domain of the mGATA-1 complementary DNA14. This was the same procedure as that used in the discovery of the ...
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Virchows Archiv 404 (1984), S. 7-16 
    ISSN: 1432-2307
    Keywords: Fibroadenoma ; Stromal cells ; Actin ; Ultrastructure ; Myofibroblast
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Fourteen fibroadenomas of the human breast were examined by light and electron microscopy, and by immunohistochemistry for actin. They were classified into 3 groups according to their stromal patterns; myxoid, fibrous-cellular and sclerotic. Actin immunohistochemistry revealed that the stromal areas were strongly positive in the fibrous-cellular group and weakly positive in the myxoid and sclerotic groups. By electron microscopy the stromal cells in most cases of the myxoid and fibrous-cellular groups were fibroblasts, containing varying amounts of microfilaments, 5–7 nm in diameter (actin type filaments). However, a dense body was not usually present suggesting these stromal cells were variants of myofibroblasts. The amount of microfilaments in fibroblasts was greater in the fibrous-cellular group than in the myxoid group. This was consistent with the results of actin immunohistochemistry. In 3 cases of the fibrous-cellular group peculiar structures simulating Z-lines of striated muscles were noted in some stromal cells. Since no myosin filaments were detected, they were regarded as intermediate structures between Z-lines of striated muscles and dense bodies of smooth muscles. In the sclerotic group, stromal fibroblasts were sparse and had fewer organelles.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Virchows Archiv 401 (1983), S. 209-222 
    ISSN: 1432-2307
    Keywords: Colorectal epithelial tumors ; Stroma ; Fibroblast ; Myofibroblast ; Smooth muscle cell
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Structural changes in stromal cells during the development of human colorectal carcinomas were studied by light and electron microscopy. The results were as follows: 1. Stromal cells of the lamina propria in control subjects consisted principally of resting fibroblasts. 2. Stromal fibroblasts were mildly activated in adenomas with mild- moderate atypia, and more markedly in adenomas with severe atypia (carcinoma in situ). 3. In invasive adenocarcinomas, (a) desmoplastic reaction was induced, (b) stromal fibroblasts proliferated significantly and were activated showing enlarged nuclei and abundant rough endoplasmic reticulum, and (c) some smooth muscle cells were endowed with well-developed rough endoplasmic reticulum in their axial cytoplasm, resulting in a similar appearance to “myofibroblasts”. 4. Stromal fibroblasts in ulcerative colitis and proctitis were also activated. Morphometric analysis revealed that activated fibroblasts significantly increased the areas of their nuclei and cytoplasm, and the perimeter of rough endoplasmic reticulum. These activated fibroblasts suggested a higher prediction of collagen and other connective tissue proteins. Bundles of microfilaments of actin type were readily found in fibroblasts in all cases examined. These filaments were most remarkable in the fibroblasts in the desmoplastic stroma of invasive adenocarcinoma and were considered to be one of the basic components of these cells. Relationships between fibroblasts, “myofibroblasts”, and smooth muscle cells are discussed.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1436-0691
    Keywords: acute cholecystitis ; gallstone ; bacterial infection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The objective of this study was to clarify the etiology of acute cholecystitis and the role of bacteria in the bile in this condition. We evaluated 52 patients with acute cholecystitis; 46 had cholesterol stones and 6 had no claculi. In the presence of cystic duct obstruction, circulatory disturbance occurs gradually, but circulatory disturbance alone cannot cause severe inflammation unless a bacterial infection is present. If there is no obstruction, rapid circulatory disturbance produces necrotic changes of the gallbladder wall, which are implicated in a fulminant course. In both instances, bacterial infection may play an important role in fulminant cholecystitis. Bacteria implicated in acute cholecystitis are usually present in the bile before the onset of this disease.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1573-2568
    Keywords: transforming growth factor-β 1 ; latent TGF-β binding protein ; colorectal adenoma ; colorectal tumorigenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Transforming growth factor-β 1 (TGF-β 1) is a multifunctional cytokine and is thought to be involved in colorectal tumorigenesis as a regulator of cell growth and differentiation. This role is mainly supported byin vitro studies while its rolein vivo remains unclear. The aim of the present study was to investigate whether the TGF-β 1 precursor (β 1-LAP) and the latent TGF-β 1 binding protein (LTBP) are expressed in colorectal adenomas, the presumed precursors of most of colorectal adenocarcinomas. TGF-β 1 precursor and LTBP were examined in 35 adenomas and 10 normal colonic mucosa specimens by immunohistochemistry, using specific polyclonal antibodies. In normal colonic mucosa,β 1-LAP was moderately expressed in epithelial crypt cells and in the stromal cells in the lamina propria. In adenomas,β 1-LAP was localized in epithelial cells with an heterogeneous pattern and was also present in stromal cells around the adenomatous glands. LTBP was not detected in epithelial cells but was observed in stromal cells and in the extracellular matrix (ECM).β 1-LAP expression in epithelial cells did not correlate with the grade of dysplasia, while LTBP localized in stromal cells and ECM appeared to be closely associated with areas of higher grade of dysplasia. This study is the first demonstration of bothβ 1-LAP and LTBP in colorectal adenomas with different dysplasia grades. Our results suggest that TGF-β 1 might be involved in the mechanisms controllingin vivo colorectal tumorigenesis and support a role for the stromal-associated TGF-β 1.
    Type of Medium: Electronic Resource
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