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  • Gelatin gels, structure  (1)
  • Key words: Bone formation — Tumor — Calvaria — Growth factor — Histomorphometry.  (1)
  • Key words Confocal microscopy  (1)
Materialart
Erscheinungszeitraum
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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Calcified tissue international 60 (1997), S. 210 -215 
    ISSN: 1432-0827
    Schlagwort(e): Key words: Bone formation — Tumor — Calvaria — Growth factor — Histomorphometry.
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin , Physik
    Notizen: Abstract. Although some tumors cause osteolytic lesions, there are some that stimulate new bone formation. This is an important phenomenon because the responsible mechanisms probably represent an aberration of normal physiological bone formation, and identifying the factors involved in the process may lead to new therapies for various bone diseases. To clarify our understanding of the potential mechanism responsible, we compared and quantitated the extent of new bone formation stimulated by human tumors (HeLa, Hep-2, AV-3, FL, WISH and KB), some of which have osteogenic activity in vivo [2]. Tumor cells were injected over the calvaria of nude mice to examine formation of new bone. The tumor cells produced three histologically distinct patterns of new bone growth: (1) WISH and KB stimulated appositional bone growth adjacent to periosteal bone surfaces; (2) HeLa and Hep2 induced new bone growth over calvarial surface even when distant from the tumor mass; (3) FL stimulated bone formation adjacent to periosteum as well as ectopic bone formation in sites distant from bone. All tumors except AV3 induced mean new bone thickness 〉100 μm, and Hep-2 cells produced bone 330 μm thick. PCR and Northern blot analysis of mRNA isolated from cultured tumor cells revealed that all cell lines expressed mRNA for TGFβ, (fibroblast growth factor) FGF-1, FGF-2, and IGF-I, and most cell lines produced mRNA for PDGF. Only FL expressed large amounts of mRNA for BMP2. In serum-free conditioned media from Hep2 and HeLa cells purified by heparin affinity chromatography, we have identified FGF-1, FGF-2, and PDGF by immunodetection with specific antibodies. Our results show that new bone growth caused by these tumors is likely due to the production of bone growth factors by the tumor cells, and that the overall effects on bone may be due to several factors working in concert.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Colloid & polymer science 269 (1991), S. 682-688 
    ISSN: 1435-1536
    Schlagwort(e): Gelatin gels, structure ; fluorescein ; translational diffusion ; holographic relaxation spectroscopy (HRS)
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Abstract The structures of gelatin gels have been studied by holographic relaxation spectroscopy (HRS) with fluorescein as a doped tracer. An HRS spectrum with double peaks has been observed. It has been experimentally proven that this “anomalous” HRS spectrum is related to the structures of the gelatin gels. It is shown that two kinds of gel networks are formed when a gelatin solution is cooled at a rate of 2°C/min to a temperature below the gel temperature. Microviscosity inside one kind of network is about four times lower than inside the other one. One with lower microviscosity is called a “coarse” network, and it is formed through aggregation of a collagen-like, triple-stranded helix. The other is named a “fine” network and it is constructed simply by entanglements between polymer chains. The structure of gelatin gel can be considered as a blend of these two networks. By controlling the cooling speed, the structure of gelatin gels can be dominated by either “coarse” or “fine” gel networks.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Colloid & polymer science 276 (1998), S. 577-588 
    ISSN: 1435-1536
    Schlagwort(e): Key words Confocal microscopy ; confocal Raman microscopy ; chemical imaging ; laser scanning confocal microscopy ; two-photon-microscopy ; fluorescence correlation spectroscopy ; Raman correlation spectroscopy
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Abstract  Modern chemical and pharmaceutical industrial research benefits from improved spectroscopic tools. New developments in confocal fluorescence and Raman microscopy lead to an increase in sensitivity, selectivity and speed of microscopic imaging and fluctuation analysis resulting in a better understanding of structure–property relationships essential for targeted development. In this paper we report on the application of fluorescence and Raman microscopy for characterizing the morphology of polymeric multiphase solid-state samples and on new developments in the corresponding correlation spectroscopies for the characterization of the dynamics of complex colloidal systems in the liquid state. In the case of fluorescence new technological opportunities are gained by two-photon excitation.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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