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一种新型钙激活钾通道控制 中的膜电位和细胞内 pH。

A Novel Calcium-Activated Potassium Channel Controls Membrane Potential and Intracellular pH in .

机构信息

Department of Biological Science, College of Natural Sciences and Mathematics, California State University Fullerton, Fullerton, CA, United States.

Departmento de Biología, Facultad de Ciencias Exactas y Naturales, Instituto de Histologia y Embriologia IHEM-CONICET, Facultad de Medicina, Universidad Nacional de Cuyo, Mendoza, Argentina.

出版信息

Front Cell Infect Microbiol. 2020 Jan 15;9:464. doi: 10.3389/fcimb.2019.00464. eCollection 2019.

Abstract

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 . 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 and shares structural features with other potassium channels. We expressed TcCAKC in 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 and provides new avenues to explore the potential of ion channels as targets for drug development against protozoan parasites.

摘要

在营养物质可用性、渗透压、离子浓度和 pH 值发生显著变化的环境中发育。适应和应对这些条件的能力决定了 的生存和成功传播。离子通道在控制通过快速触发补偿机制确保细胞内稳态的生理参数方面发挥着基本作用。通过结合分子、细胞和电生理方法,我们已经鉴定和表征了一种新型钙激活钾通道(TcCAKC)的表达和功能。该通道存在于 和所有 3 个生活阶段的质膜中,与其他钾通道具有结构特征。我们在 卵母细胞中表达了 TcCAKC,并通过双电极电压钳法确定了其生物物理特性。表达 TcCAKC 的卵母细胞在添加钙离子载体离子霉素或 thapsigargin 后,内向电流显著增加。这些反应被 EGTA 消除,表明 TcCAKC 的激活依赖于细胞外钙。这种激活导致电流增加和反转电位负移,被钡阻断。正如预测的那样,选择性过滤器中的单点突变(Y313A)完全消除了通道的活性,证实了其钾选择性。我们已经生成了缺失 TcCAKC 的一个或两个等位基因的敲除寄生虫。这些寄生虫株表现出生长受损、产生的锥虫减少和细胞内复制速度减慢,表明 TcCAKC 在调节感染力方面起着重要作用。为了了解这些表型缺陷背后的细胞机制,我们使用荧光探针评估了细胞内膜电位、pH 值和细胞内钙。缺乏通道的 epimastigotes 具有显著较低的细胞质钙、超极化、细胞内 pH 值变化和质子外排率增加。这些结果与先前的报告一致,表明在原生动物中,膜电位和细胞内 pH 值的维持是相关的。我们的工作表明,TcCAKC 是一种新型钾通道,有助于 和重要生理过程的内稳态调节,并为探索离子通道作为针对原生动物寄生虫的药物开发靶点的潜力提供了新途径。

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