Abstract

Trypanosoma cruzi develops in environments where nutrient availability, osmolarity, ionic concentrations, and pH undergo significant changes. The ability to adapt and respond to such conditions determines the survival and successful transmission of T. cruzi. Ion channels play fundamental roles in controlling physiological parameters that ensure cell homeostasis by rapidly triggering compensatory mechanisms. Combining molecular, cellular and electrophysiological approaches we have identified and characterized the expression and function of a novel calcium-activated potassium channel (TcCAKC). This channel resides in the plasma membrane of all 3 life stages of T. cruzi and shares structural features with other potassium channels. We expressed TcCAKC in Xenopus laevis oocytes and established its biophysical properties by two-electrode voltage clamp. Oocytes expressing TcCAKC showed a significant increase in inward currents after addition of calcium ionophore ionomycin or thapsigargin. These responses were abolished by EGTA suggesting that TcCAKC activation is dependent of extracellular calcium. This activation causes an increase in current and a negative shift in reversal potential that is blocked by barium. As predicted, a single point mutation in the selectivity filter (Y313A) completely abolished the activity of the channels, confirming its potassium selective nature. We have generated knockout parasites deleting one or both alleles of TcCAKC. These parasite strains showed impaired growth, decreased production of trypomastigotes and slower intracellular replication, pointing to an important role of TcCAKC in regulating infectivity. To understand the cellular mechanisms underlying these phenotypic defects, we used fluorescent probes to evaluate intracellular membrane potential, pH, and intracellular calcium. Epimastigotes lacking the channel had significantly lower cytosolic calcium, hyperpolarization, changes in intracellular pH, and increased rate of proton extrusion. These results are in agreement with previous reports indicating that, in trypanosomatids, membrane potential and intracellular pH maintenance are linked. Our work shows TcCAKC is a novel potassium channel that contributes to homeostatic regulation of important physiological processes in T. cruzi and provides new avenues to explore the potential of ion channels as targets for drug development against protozoan parasites.

Highlights

  • Ion homeostasis is central to all life forms

  • BlastP analysis of Trypanosoma sequences only shows significant homology with sequences encoding for calcium-activated potassium channels (CAKCs), the overall identity is below 20%

  • Unlike CAKCs of large conductance, TcCAKC does not possess calcium binding sites, suggesting that its activation is rather mediated by Ca2+Calmodulin binding, as it has been shown for IK and SK channels

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Summary

Introduction

Ion homeostasis is central to all life forms. Cellular composition must to be regulated in a dynamic manner in order to preserve a relatively constant intracellular environment, even under the most extreme external changes (Pasantes-Morales, 2016). Ion channels play a role in controlling a wide array of important physiological processes including membrane potential regulation, pH, cell volume, cell proliferation, and death (Lang et al, 2007; Bae et al, 2011; Pasantes-Morales, 2016). They are validated targets for treatment of highly prevalent diseases such as cardiovascular pathologies (Gill et al, 1992; Turley et al, 2016) and are currently being re-evaluated as potential drug targets against parasitic infections (Meier et al, 2018). Ion channel characterization lags behind the general progress of the field, mostly due to technical limitations for direct electrophysiological recordings in motile cells, but in recent years we have gained insight into the role of calcium channels in trypanosomes (Chiurillo et al, 2017; Huang and Docampo, 2018; Potapenko et al, 2019; Rodriguez-Duran et al, 2019)

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