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Intracellular calcium homeostasis in Leishmania mexicana. Identification and characterization of a plasma membrane calmodulin-dependent Ca(2+)-ATPase
Benaim, Gustavo; Cervino, Vincenza; Hermoso, Tomas; Felibert, P; Laurentin, Alexander.
  • Benaim, Gustavo; Universidad Central de Caracas. Centro de Biología Celular.
  • Cervino, Vincenza; Universidad Central de Caracas. Centro de Biología Celular.
  • Hermoso, Tomas; Universidad Central de Caracas. Centro de Biología Celular.
  • Felibert, P; Universidad Central de Caracas. Centro de Biología Celular.
  • Laurentin, Alexander; Universidad Central de Caracas. Centro de Biología Celular.
Biol. Res ; 26(1/2): 141-50, 1993. graf
Article in English | LILACS | ID: lil-228601
RESUMO
The intracellular Ca2+ concentration in different trypanosomatids is about 50 nanomolar, which concentration in different trypanosomatids is about 50 nanomolar, which is 4 orders of magnitude lower than in the extracellular milieu. This fact implies the existence of well developed mechanisms for the maintenance of such a high calcium gradient. In higher eukaryotics a number of different structures have been implicated in this function. Some of them are located in intracellular organelles, and others in the plasma membrane. Since intracellular organelles are limited by their storage capacity, long-term Ca2+ homeostasis resides solely in the plasma membrane. In higher eukaryotics, a calcium pump or Ca(2+)-ATPase located in the plasma membrane, because of its high Ca2+ affinity, has been proposed as the structure responsible for the maintenance of the cytoplasmic Ca2+ concentration at the submicromolar level. The presence of a Ca(2+)-ATPase in trypanosomatids has been debated. While some groups have reported its absence, others have reported the existence of an enzyme which is Mg(2+)-independent or even inhibited by Mg2+. On the other hand, in none of these reports any correlation was shown between the Ca(2+)-ATPase activity observed and the Ca2+ transport function attributed to this enzyme. We have previously shown that a calmodulin-stimulated Mg(2+)-dependent Ca(2+)-ATPase is present in the plasma membrane of Leishmania braziliensis and of Trypanosoma cruzi. Plasma membrane vesicles from these parasites are able to accumulate Ca2+ in the presence of the ATP-Mg complex. The similarities found between the kinetics parameters and other properties of the Ca(2+)-ATPase and the Ca2+ transport activity strongly suggest a common molecular entity. The stoichiometry calculated from these parameters approaches the 11 stoichiometry for Ca2+ and ATP, as reported for the Ca2+ pump from higher eukaryotic cells. In this report we show that plasma membrane vesicles from Leishmania mexicana possess a Ca(2+)-ATPase with characteristics which are similar to that reported by us for other trypanosomatids. Thus, the enzyme has a high Ca2+ affinity which is further increased upon addition of calmodulin. The maximal velocity is also increased by calmodulin...
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Index: LILACS (Americas) Main subject: Leishmania mexicana / Calmodulin / Calcium / Calcium-Transporting ATPases / Homeostasis / Intracellular Membranes Type of study: Diagnostic study / Prognostic study Limits: Animals / Humans Country/Region as subject: Mexico Language: English Journal: Biol. Res Journal subject: Biology Year: 1993 Type: Article

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Index: LILACS (Americas) Main subject: Leishmania mexicana / Calmodulin / Calcium / Calcium-Transporting ATPases / Homeostasis / Intracellular Membranes Type of study: Diagnostic study / Prognostic study Limits: Animals / Humans Country/Region as subject: Mexico Language: English Journal: Biol. Res Journal subject: Biology Year: 1993 Type: Article