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suck abstract from ncbi


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pmid2950094      J+Biol+Chem 1987 ; 262 (7): 3118-22
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  • Extracellular ATP4- promotes cation fluxes in the J774 mouse macrophage cell line #MMPMID2950094
  • Steinberg TH; Silverstein SC
  • J Biol Chem 1987[Mar]; 262 (7): 3118-22 PMID2950094show ga
  • Extracellular ATP stimulates transmembrane ion fluxes in the mouse macrophage cell line J774. In the presence of Mg2+, nonhydrolyzable ATP analogs and other purine and pyrimidine nucleotides do not elicit this response, suggesting the presence of a specific receptor for ATP on the macrophage plasma membrane. One candidate for such a receptor is the ecto-ATPase expressed on these cells. We, therefore, investigated the role of this enzyme in ATP-induced 86Rb+ efflux in J774 cells. The ecto-ATPase had a broad nucleotide specificity and did not hydrolyze extracellular ATP in the absence of divalent cations. 86Rb+ efflux was not blocked by inhibition of the ecto-ATPase and did not require Ca2+ or Mg2+. In fact, ATP-stimulated 86Rb+ efflux was inhibited by Mg2+ and correlated with the availability of ATP4- in the medium. In the absence of divalent cations, the slowly hydrolyzable ATP analogs adenosine 5'-(beta, gamma-imido)triphosphate (AMP-PNP) and adenosine 5'-O-(3-thio)triphosphate (ATP-gamma-S) also stimulated 86Rb+ efflux, albeit at higher concentrations than that required for ATP4-. Exposure of J774 cells to 10 mM ATP for 45 min caused death of 95% of cells. By this means we selected variant J774 cells that did not exhibit 86Rb+ efflux in the presence of extracellular ATP but retained ecto-ATPase activity. These results show that the ecto-ATPase of J774 cells does not mediate the effects of ATP on these cells; that ATP4- and not MgATP2- promotes 86Rb+ efflux from these cells; and that hydrolysis of ATP is not required to effect this change in membrane permeability. These findings suggest that J774 cells possess a plasma membrane receptor which binds ATP4-, AMP-PNP, and ATP-gamma-S, and that the ecto-ATPase limits the effects of ATP on these cells by hydrolyzing Mg-ATP2-.
  • |Adenosine Triphosphatases/metabolism[MESH]
  • |Adenosine Triphosphate/analogs & derivatives/metabolism/*pharmacology[MESH]
  • |Adenylyl Imidodiphosphate/pharmacology[MESH]
  • |Animals[MESH]
  • |Calcium/pharmacology[MESH]
  • |Cations, Monovalent[MESH]
  • |Cell Line[MESH]
  • |Kinetics[MESH]
  • |Macrophages/drug effects/*metabolism[MESH]
  • |Magnesium/pharmacology[MESH]
  • |Mice[MESH]
  • |Nucleotides/pharmacology[MESH]
  • |Radioisotopes[MESH]


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