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Chip-calorimetric assessment of heat generation during Ca2+ uptake by digitonin-permeabilized Trypanosoma cruzi

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TLDR
In this article, the authors evaluated the heat generation during Ca2+ uptake by digitonin-permeabilized T. cruzi epimastigotes, a system consisting of Ca2+, uptake predominantly by mitochondria and acidocalcisomes.
Abstract
Ca2+ signaling in trypanosomatids is an important component of energy metabolism regulation and therefore, cytosolic Ca2+ concentration is finely regulated by Ca2+ transport through the plasma membrane and Ca2+ uptake and release by intracellular organelles. To maintain intracellular Ca2+ homeostasis with different gradients of the ion within the cellular compartments, there is an energy cost and also energy dissipation in the form of heat. Using an innovative segmented fusion technique of a chip-calorimeter and CRISPR/Cas9 knockout (–KO) Trypanosoma cruzi cell lines, we evaluated the heat generation during Ca2+ uptake by digitonin-permeabilized T. cruzi epimastigotes, a system consisting of Ca2+ uptake predominantly by mitochondria and acidocalcisomes. We used three T. cruzi epimastigotes cell lines: control cells denominated scrambled, cells with the absence of the pyruvate dehydrogenase phosphatase (TcPDP-KO) and cells lacking mitochondrial Ca2+ uptake via the mitochondrial calcium uniporter (TcMCU-KO), that presented, in this respective order, decreasing rates and capacities of Ca2+ uptake. TcPDP-KO cells exhibited the lowest heat production following Ca2+ addition, which may be due to its lower mitochondrial oxidative phosphorylation capacity and lower ATP availability for acidocalcisomal Ca2+ uptake. Scrambled and TcMCU-KO cells exhibited similar Ca2+-induced heat effects, which correlates with a higher ATP-dependent acidocalcisomal Ca2+ uptake in these cells. Our results show evidences that mitochondrial Ca2+ transport via the uniporter is minimally heat dissipative, while ATPase pumps in acidocalcisomes possess a predominant contribution to the heat generated during Ca2+ uptake.

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Journal ArticleDOI

Feeding effects on liver mitochondrial bioenergetics of Boa constrictor (Serpentes: Boidae).

TL;DR: In this article, the authors compared liver mitochondrial bioenergetics of the boid snake Boa constrictor during fasting and after meal intake, and concluded that liver mitochondria from B. constrictors increase respiration rates during the post-prandial period and quickly improve the bioenergetic capacity without compromising redox balance.
Posted ContentDOI

Feeding effects on liver mitochondrial bioenergetics of Boa constrictor (Serpentes: Boidae)

TL;DR: In this paper, the authors compared liver mitochondrial bioenergetics of the boid snake Boa constrictor during fasting and after meal intake, and found that liver mitochondria from B. constrictors increased the maintenance costs during the post-prandial period and quickly improved the mitochondria capacity without compromising the redox balance.
Journal ArticleDOI

Enhanced resistance to Ca2+-induced mitochondrial permeability transition in the long-lived red-footed tortoise <i>Chelonoidis carbonaria</i>

TL;DR: In this article , the authors compared the liver mitochondrial Ca2+ retention capacity and oxygen consumption in the long-lived red-footed tortoise (Chelonoidis carbonaria) with those in the rat as a reference standard.
References
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Journal ArticleDOI

Mitochondrial Membrane Permeabilization in Cell Death

TL;DR: Once MMP has been induced, it causes the release of catabolic hydrolases and activators of such enzymes (including those of caspases) from mitochondria, meaning that mitochondria coordinate the late stage of cellular demise.
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Mitochondria as sensors and regulators of calcium signalling

TL;DR: During the past two decades calcium (Ca2+) accumulation in energized mitochondria has emerged as a biological process of utmost physiological relevance, opening new perspectives for investigation and molecular intervention.
Journal ArticleDOI

Role of calcium ions in regulation of mammalian intramitochondrial metabolism

TL;DR: Ce rapport de synthese tente de fournir une vue generale sur les relations possibles qui existent entre les effets du Ca 2+ a l'interieur des mitochondries and le besoin d'ATP reclame par les cellules des vertebres.
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MICU1 encodes a mitochondrial EF hand protein required for Ca 2+ uptake

TL;DR: An integrative strategy is used to predict human genes involved in mitochondrial calcium entry based on clues from comparative physiology, evolutionary genomics and organelle proteomics, and finds MICU1 represents the founding member of a set of proteins required for high-capacity mitochondrial calcium uptake.
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