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  • Key words: Volume regulation — Phosphoinositidase C — Ins(1,4,5)P3— Ca2+signaling — K+ channels — Charybdotoxin — Clotrimazole  (1)
  • Springer  (1)
  • Wiley-Blackwell
  • Canadian Society of Petroleum Geologists (CSPG)
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  • Springer  (1)
  • Wiley-Blackwell
  • Canadian Society of Petroleum Geologists (CSPG)
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  • 1
    ISSN: 1432-1424
    Keywords: Key words: Volume regulation — Phosphoinositidase C — Ins(1,4,5)P3— Ca2+signaling — K+ channels — Charybdotoxin — Clotrimazole
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract. The putative role for Ca2+ entry and Ca2+ mobilization in the activation of the regulatory volume decrease (RVD) response has been assessed in Ehrlich cells. Following hypotonic exposure (50% osmolarity) there is: (i) no increase in cellular Ins(1,4,5)P3 content, as measured in extracts from [2-3H]myoinositol-labeled cells, a finding at variance with earlier reports from our group; (ii) no evidence of Ca2+-signaling recorded in a suspension of fura-2-loaded cells; (iii) Ca2+-signaling in only about 6% of the single, fura-2-loaded cells at 1-mm Ca2+ (1% only at 0.1-mm Ca2+ and in Ca2+-free medium), as monitored by fluorescence-ratio imaging; (iv) no effect of removing external Ca2+ upon the volume-induced K+ loss; (v) no significant inhibition of the RVD response in cells loaded with the Ca2+ chelator BAPTA when the BAPTA-loading is performed in K+ equilibrium medium; (vi) an inhibition of the swelling-induced K+ loss (about 50%) at 1-mm Ba2+, but almost no effect of charybdotoxin (100 nm) or of clotrimazole (10 μm), reported inhibitors of the K+ loss induced by Ca2+-mobilizing agonists. Thus, Ca2+signaling by Ca2+ release or Ca2+ entry appears to play no role in the activation mechanism for the RVD response in Ehrlich cells.
    Type of Medium: Electronic Resource
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