Lanthanides are transported by ionophore A23187 and mimic calcium in the histamine secretion process

1 Ionophore A23187 induced histamine release from peritoneal rat mast cells in the presence of lanthanum or terbium as it did in the presence of calcium. 2 Low concentrations of lanthanides (10−5 to 2 × 10−4m) were more efficient than similar concentrations of calcium. 3 The effect of low concentrations of calcium and lanthanides were additive. 4 Increasing the concentration of lanthanides above 10−3 m decreased histamine release. This decrease was partly reversed by calcium. 5 Calmodulin inhibitors, phenothiazines, R24571 and mepacrine, inhibited the histamine release induced by either calcium or lanthanides. 6 Zn2+, a calmodulin inhibitor transported by A23187, inhibited more potently the calcium‐dependent histamine release. 7 Lanthanides decrease histamine release induced by 48/80 in the absence of added calcium. 8 These data show that ionophore A23187 can transport lanthanides across the plasma membrane of mast cells, allowing the trivalent cations to substitute for calcium in the activation of calmodulin or calmoduline‐like proteins.

[1]  B. Weiss,et al.  Interaction of drugs with calmodulin. Biochemical, pharmacological and clinical implications. , 1982, Biochemical pharmacology.

[2]  R. Wallace,et al.  Calcium binding domains of calmodulin. Sequence of fill as determined with terbium luminescence. , 1982, The Journal of biological chemistry.

[3]  W. Douglas,et al.  On the calcium receptor activating exocytosis: inhibitory effects of calmodulin‐interacting drugs on rat mast cells. , 1982, The Journal of physiology.

[4]  F. Crews,et al.  Phospholipase activation in the IgE-mediated and Ca2+ ionophore A23187-induced release of histamine from rat basophilic leukemia cells. , 1981, Archives of biochemistry and biophysics.

[5]  H. Belle R 24 571: A potent inhibitor of calmodulin-activated enzymes , 1981 .

[6]  M. Ruckstuhl,et al.  Can calmodulin inhibitors be used to probe calmodulin effects? , 1981, Biochemical pharmacology.

[7]  L. Lichtenstein,et al.  Modulation of histamine release from human basophils in vitro by physiological concentrations of zinc. , 1981, The Journal of pharmacology and experimental therapeutics.

[8]  J. White,et al.  EFFECT OF LANTHANIDE IONS ON HISTAMINE SECRETION FROM RAT PERITONEAL MAST CELLS , 1981, British journal of pharmacology.

[9]  P. Epstein,et al.  Local anesthetics, mepacrine, and propranolol are antagonists of calmodulin. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[10]  T. Molski,et al.  Calmodulin inhibitors block neutrophil degranulation at a step distal from the mobilization of calcium. , 1980, Biochemical and biophysical research communications.

[11]  J. Demaille,et al.  Terbium binding to octopus calmodulin provides the complete sequence of ion binding , 1980, FEBS letters.

[12]  M. Church,et al.  INHIBITION OF HISTAMINE RELEASE FROM HUMAN LUNG in vitro BY ANTIHISTAMINES AND RELATED DRUGS , 1980, British journal of pharmacology.

[13]  J. Demaille,et al.  Terbium as luminescent probe of calmodulin calcium‐binding sites , 1980, FEBS letters.

[14]  A. H. Drummond,et al.  Inhibition of calcium-dependent regulator-stimulated phosphodiesterase activity by neuroleptic drugs is unrelated to their clinical efficacy. , 1979, Molecular pharmacology.

[15]  J. Aster,et al.  Zinc inhibition of calmodulin: A proposed molecular mechanism of zinc action on cellular functions , 1979, American journal of hematology.

[16]  L. Lichtenstein,et al.  Spontaneous histamine secretion from leukocytes in the presence of strontium. , 1979, The Journal of pharmacology and experimental therapeutics.

[17]  R. Martin,et al.  Lanthanides as probes for calcium in biological systems , 1979, Quarterly Reviews of Biophysics.

[18]  M. Belmont,et al.  Rate-determining processes in the transport of Pr3+ ions by the ionophore A23187 across phospholipid vesicular membranes. A 1H-MR and theoretical study. , 1978, Biophysical chemistry.

[19]  H. Lardy,et al.  Ionophore A23187: the effect of H+ concentration on complex formation with divalent and monovalent cations and the demonstration of K+ transport in mitochondria mediated by A23187. , 1976, Biochemistry.

[20]  H. Lardy,et al.  Ultraviolet and fluorescent spectral properties of the divalent cation ionophore A23187 and its metal ion complexes. , 1974, Biochemistry.

[21]  J. Foreman,et al.  Calcium Ionophores and Movement of Calcium Ions following the Physiological Stimulus to a Secretory Process , 1973, Nature.

[22]  J. Foreman,et al.  The action of lanthanum and manganese on anaphylactic histamine secretion , 1973, British journal of pharmacology.

[23]  J. Foreman,et al.  Dual effect of lanthanum on histamine release from mast cells. , 1972, Nature: New biology.

[24]  B. Högberg,et al.  Further observations on the disruption of rat mesentery mast cells caused by compound 48/80, antigen-antibody reaction, lecithinase A and decylamine. , 1960 .

[25]  P. A. Shore,et al.  A method for the fluorometric assay of histamine in tissues. , 1959, The Journal of pharmacology and experimental therapeutics.

[26]  Bertil Höugberg,et al.  The Mechanism of the Disruption of Mast Cells Produced by Compound 48/801 , 1957 .

[27]  J. Foreman The pharmacological control of immediate hypersensitivity. , 1981, Annual review of pharmacology and toxicology.

[28]  B. Uvnas,et al.  The mechanism of the disruption of mast cells produced by compound 48/80. , 1957, Acta physiologica Scandinavica.