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  • ATP  (1)
  • Adeno-associated virus  (1)
  • Antibody response dynamics  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 213 (1989), S. 61-72 
    ISSN: 0027-5107
    Keywords: Adeno-associated virus ; DNA amplification ; SV40 ; Tumorigenicity
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2013
    Keywords: Cl− conductance ; K+ conductance ; ATP ; Bradykinin ; Histamine ; Bronchial epithelial cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The present study was performed to examine Ca2+-dependent and cell-swelling-induced ion conductances in a polarized bronchial epithelial cell line (16HBE14o-). Whole-cell currents were measured in fast and slow whole-cell patch-clamp experiments in cells grown either on filters or on coated plastic dishes. In addition the transepithelial voltage (V te) and resistance (R te) were measured in confluent monolayers. Resting cells had a membrane voltage (V m) of −36±1.1 mV (n=137) which was mainly caused by K+ and Cl− conductances and to a lesser extent by a Na+ conductance. V te was apical-side-negative after stimulation. Equivalent short-circuit current (I sc = V te/R te) was increased by the secretagogues histamine (0.1 mmol/l), bradykinin (0.1–10 μmol/l) and ATP (0.1–100 μmol/l). The histamine-induced I sc was blocked by either basolateral diphenhydramine (0.1 mmol/l, n=4) or apical cimetidine (0.1 mmol/l, n=4). In fast and slow whole-cell recordings ATP and bradykinin primarily activated a transient K+ conductance and hyperpolarized V m. This effect was mimicked by the Ca2+ ionophore ionomycin (1 μmol/l, n=11). Inhibition of the bradykinin-induced I sc by the blocker HOE140 (1 μmol/l, n=3) suggested the presence of a BK2 receptor. The potency sequence of different nucleotide agonists on the purinergic receptor was UTP ≈ ATP 〉 ITP 〉 GTP ≈ CTP ≈ [β,γ-methylene] ATP ≈ 2-methylthio-ATP = 0 and was obtained in I sc measurements and patch-clamp recordings. This suggests the presence of a P2u receptor. Hypotonic cell swelling activated both Cl− and K+ conductances. The Cl− conductance was only slightly inhibited by 4,4′-diisothiocyanatostilbene-2,2′-disulphonic acid (0.5 mmol/ l, n=3). These data indicate that 16HBE140- bronchial epithelial cells, which are known to express high levels of cystic fibrosis transmembrane conductance regulator protein, form a secretory epithelium. While hypotonic cell swelling activates both K+ and Cl− channels, the Ca2+-induced Cl− secretion is due mainly to activation of basolateral K+ channels.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of mathematical biology 13 (1981), S. 67-86 
    ISSN: 1432-1416
    Keywords: Antibody response dynamics ; B lymphocyte differentiation ; Control by antigen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Mathematics
    Notes: Abstract A mathematical model of B lymphocyte differentiation, based on experimental results, has been developed. The model focuses on the role of antigen in initiating and regulating B cell differentiation while other mechanisms, acting in concert with antigen but the functioning of which can be circumvented under appropriate conditions, are not considered. The importance of presence of antigen at individual stages of B cell differentiation was studied in experiments with an easily metabolizable antigen. Immunocompetent cells (ICC), arising by antigen-independent differentiation of stem cells, are activated by antigen (they become immunologically activated cells — IAC). Excess of antigen drives IAC into the terminal stage (antibody-forming cells — AFC) thereby restricting proliferation. Exhaustive terminal differentiation results in tolerance. A low primary dose permits IAC to escape antigen; IAC proliferate and later give rise to resting memory cells (MC) which are amenable to reactivation. MC have higher avidity for antigen (due to higher affinity, number and density of receptors) and the effect of different doses of antigen on MC is diverse. A very low secondary dose induces tolerance, a medium dose secondary response, and the administration of a high dose of antigen also brings about tolerance. The model suggests that the fate of memory cells is controlled by the ratio R∶Ag, of the number of immunoglobulin receptors on B cells (R) to the number of available antigenic molecules (Ag), low values of R∶Ag favouring stimulation to differentiation while high values of R∶Ag favouring inactivation. A nonlinear system of ordinary differential equations, describing the development of the populations involved in antigen driven B cell differentiation, was used to simulate experiments and good qualitative agreement was achieved.
    Type of Medium: Electronic Resource
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