Laboratório de Bioquímica de Tripanosomatideos, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz - FIOCRUZ, Pavilhão Leônidas Deane, 4 degrees andar, sala 405, Manguinhos, 21045-900 Rio de Janeiro, RJ, Brazil.
Exp Parasitol. 2010 Apr;124(4):436-41. doi: 10.1016/j.exppara.2009.12.012. Epub 2010 Jan 4.
In the present paper we studied the involvement of the phosphatidylinositol-specific PLC (PI-PLC)/protein kinase C (PKC) pathway in (Na(+)+K(+))ATPase stimulation by heme in Leishmania amazonensis promastigotes. Heme stimulated the PKC-like activity with a concentration of 50nM. Interestingly, the maximal stimulation of the PKC-like activity promoted by phorbol ester was of the same magnitude promoted by heme. However, the stimulatory effect of heme is completely abolished by ET-18-OCH(3) and U73122, specific inhibitors of PI-PLC. (Na(+)+K(+))ATPase activity is increased in the presence of increased concentrations of heme, being maximally affected at 50nM. This effect was completely reversed by 10nM calphostin C, an inhibitor of PKC. Thus, the effect of 50nM heme on (Na(+)+K(+))ATPase activity is completely abolished by ET-18-OCH(3) and U73122. Taken together, these results demonstrate that the heme receptor mediates the stimulatory effect of heme on the (Na(+)+K(+))ATPase activity through a PI-PLC/PKC signaling pathway.
在本研究中,我们研究了磷脂酰肌醇特异性 PLC(PI-PLC)/蛋白激酶 C(PKC)途径在血红素刺激莱氏利什曼原虫前鞭毛体(Na(+)+K(+))ATP 酶中的作用。血红素以 50nM 的浓度刺激 PKC 样活性。有趣的是,佛波酯刺激的 PKC 样活性的最大刺激与血红素刺激的活性相同。然而,血红素的刺激作用完全被 PI-PLC 的特异性抑制剂 ET-18-OCH(3) 和 U73122 所消除。在血红素浓度增加的情况下,(Na(+)+K(+))ATP 酶活性增加,在 50nM 时达到最大值。这种作用完全被 PKC 抑制剂 calphostin C(10nM)所逆转。因此,50nM 血红素对(Na(+)+K(+))ATP 酶活性的影响完全被 ET-18-OCH(3) 和 U73122 所消除。综上所述,这些结果表明血红素受体通过 PI-PLC/PKC 信号通路介导血红素对(Na(+)+K(+))ATP 酶活性的刺激作用。