| 16380977 |
Entringer PF, Gondim KC, Meyer-Fernandes JR: Ecto-nucleotidase activities in the fat body of Rhodnius prolixus. Arch Insect Biochem Physiol. 2006 Jan;61(1):1-9.
In this study, we describe the ability of intact fat body of an insect, Rhodnius prolixus, to hydrolyze extracellular ATP. In these fat bodies, the ATP hydrolysis was low in the absence of any divalent metal, and was stimulated by MgCl (2). Both activities (in the absence or presence of MgCl (2)) were linear with time for at least 30 min. In order to confirm the observed nucleotidase activities as ecto-nucleotidases, we used an impermeant inhibitor, DIDS (4, 4'-diisothiocyanostylbene 2'-2'-disulfonic acid). This reagent inhibited both nucleotidase activities and its inhibitory effect was suppressed by ATP. Both ecto-nucleotidase activities were insensitive to inhibitors of other ATPase and phosphatase activities, such as oligomycin, sodium azide, bafilomycin, ouabain, vanadate, molybdate, sodium fluoride, levamizole, tartrate, p-NPP, sodium phosphate, and suramin. Concanavalin A, activator of some ecto-ATPases, was able to stimulate the Mg (2+)-independent nucleotidase activity, but not the Mg (2+)-dependent one. The Mg (2+)-independent nucleotidase activity was enhanced with increases in the pH in the range between 6.4-8.0, but the Mg (2+)-dependent nucleotidase activity was not affected. Besides MgCl (2) , the ecto-ATPase activity was also stimulated by CaCl (2),() MnCl (2), and SrCl (2), but not by ZnCl (2). ATP, ADP, and AMP were the best substrates for the Mg (2+)-dependent ecto-nucleotidase activity, and CTP, GTP, and UTP produced very low reaction rates. However, the Mg (2+)-independent nucleotidase activity recognized all these nucleotides producing similar reaction rates, but GTP was a less efficient substrate. The possible role of the two ecto-nucleotidase activities present on the cell surface of fat body of Rhodnius prolixus, which are distinguished by their substrate specificity and their response to Mg (2+), is discussed. |
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