Determination of Intracellular Ca 2+ Concentration in the Human Pathogens Trypanosomatids Leishmania mexicana and Trypanosoma cruzi by the Use of the Fluorescent Ca 2+ Indicator Fura-2.

Ca ²⁺ is an essential signaling messenger in all eukariotic cells, playing a pivotal role in many cellular functions as cell growth control (differentiation, fertilization and apoptosis), secretion, gene expression, enzyme regulation, among many others. This basic premise includes trypanosomatids as Trypanosoma cruzi and various species of Leishmania , the causative agents of Chagas disease and leishmaniasis respectively, where intracellular Ca ²⁺ concentration ([Ca ²⁺ ] _i ) has been demonstrated to be finely regulated. Nevertheless [Ca ²⁺ ] _i has been difficult to measure because of its very low cytoplasmic concentration (typically around 50-100 nM), when compared to the large concentration in the outside milieu (around 2 mM in blood). The development of intracellular fluorescent Ca ²⁺ -sensitive indicators has been of paramount importance to achieve this goal. The success was based on the synthesis of acetoximethylated derivative precursors, which allow the fluorescent molecules typically composed of many hydrophilic carboxyl groups responsible for its high affinity Ca ²⁺ -binding (and therefore very hydrophilic), to easily cross the plasma membrane. Once in the cell interior, unspecific esterases split the hydrophobic moiety from the fluorescent backbone structure, releasing the carboxyl groups, transforming it in turn to the acid form of the molecule, which remain trapped in the cytoplasm and regain its ability to fluoresce in a Ca ²⁺ -dependent manner. Among them, Fura-2 is by far the most used, because it is a ratiometric (two different wavelength excitation and one emission) Ca ²⁺ indicator with a Ca ²⁺ affinity compatible with the [Ca ²⁺ ] _i . This protocol essentially consists in loading exponential phase parasites with Fura-2 and recording changes in [Ca ²⁺ ] _i by mean of a double wavelength spectrofluorometer. This technique allows the acquisition of valuable information about [Ca ²⁺ ] _i changes in real time, as a consequence of diverse stimuli or changes in conditions, as addition of drugs or different natural modulators.
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