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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Molecular and cellular biochemistry 140 (1994), S. 49-54 
    ISSN: 1573-4919
    Keywords: capillary endothelial cells ; β-adrenoreceptor ; cell proliferation ; endothelial cell culture ; angiogenesis ; adenylate cyclase-cAMP system
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract β-Adrenoreceptor has been studied in a clonal capillary endothelial cell line established from the vascular bed of the bovine adrenal medulla. [3H]Dihydroalprenolol ([3H]DHA) binding to the isolated plasma membranes from these cells has demonstrated the presence of β-adrenoreceptors with two different affinities. the dissociation constants (Kd) have been found to be 0.27±0.09×10−9 M and 2.96±0.31×10−9 M, respectively with the corresponding Bmax of 5.1±0.05 and 70.0±0.2 pmol/mg protein, respectively. Inhibition of [3H]DHA binding to the β-receptor by atenolol (a β1-antagonist) and ICI 118,551 (a β1-antagonist) has suggested that the IC50cor (=Ki) for atenolol and ICI 118,551 for high affinity site are 0.08±0.03×10−12 M and 0.25±0.08×10−12 M, respectively. This, therefore, indicates that both atenolol and ICI 118,551 are able to displace the bound ligand effectively but the β1-selective antagonist atenolol is 3 times more potent than its β2 counterpart, ICI 118,551. Displacement of [3H]DHA binding to the endothelial cell plasma membrane by the agonists isoproterenol, epinephrine and norephinephrine has established a relative order of Ki for these agents as isoproterenol (0.56±0.19×10−9 M)〈epinephrine (0.77±0.26−9 M)〉-norepinephrine (0.71±0.24×10−9 M) for the high affinity site. The corresponding values for the low affinity site, however, are 4.62±0.64×10−9 M, 6.21±0.86×10−9 M and 5.90±0.82×10−9 M, respectively for the same agonists. Increased intracellular cAMP accompanied with cellular proliferation in the presence of isoproterenol has suggested not only the coupling of β-adrenoreceptors to the adenylate cyclase system but also its involvement in endothelial cell proliferation.
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  • 2
    ISSN: 1573-4919
    Keywords: estrogen ; angiogenesis ; endothelial cells ; adhesion ; proliferation ; capillary formation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Abnormal angiogenesis underlies many pathological conditions and is critical for the growth and maintenance of various types of tumors, including hormone-dependent cancers. Since estrogens are potent carcinogens in humans and rodents, and are involved in regulating angiogenesis, this study was designed to examine the effect of estrogen on the behavior of an established bovine capillary endothelial cell line, a simple and physiologically relevant model of the capillary wall. The results demonstrate that 17β-estradiol (E2), at different conditions, exerts both stimulatory and inhibitory effects on endothelial cell adhesion, proliferation and tube formation in vitro. Utilizing a cellular attachment assay, chronic exposure to nanomolar concentrations of E2 (i.e. 1 and 10 nM) increased endothelial cell adhesion significantly compared to vehicle treated controls. Cellular adhesion was inhibited by micromolar concentrations of E2. Cell count, PCNA immunohistochemistry and Western blot analysis demonstrated enhanced cell proliferation at low E2 concentration in estrogen-deplete medium. Inhibition of cellular proliferation was observed in both estrogen-replete and deplete medium at higher E2 concentrations (i.e. 1 and 10 µM). Furthermore, in vitro tube formation increased up to 3.0 fold in the presence of 10 nM and higher E2 concentrations. The present observations indicate that in vitro regulation of capillary endothelial cell adhesion, proliferation and capillary tube formation by estrogen, are dose dependent.
    Type of Medium: Electronic Resource
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