1. Introduction
Hypoxia/ischemia is a widespread phenomenon that occurs both in conditions of oxygen deficiency in the environment and in various pathologies as a result of a decrease in oxygen delivery to the cell to a level insufficient to maintain its functions and structure. Hypoxic conditions in the body are observed in ischemic and reperfusion injuries of organs, hemodynamic disorders, coronary insufficiency, blood loss, hemorrhagic shock, arterial hypertension, pulmonary insufficiency, systemic inflammatory response syndrome, traumatic shock, exposure to adverse environmental factors, extreme conditions, and other stressful effects.
The main intracellular targets of hypoxia of various etiologies are mitochondria and aerobic energy metabolism [
1,
2]. Hypoxia alters mitochondrial dynamics and morphology and provokes mitochondrial dysfunction, which can lead to a drop in the ATP synthesis, an increase in the production of reactive oxygen species, and other adverse events, including the disturbance of ionic, mainly Ca
2+, homeostasis. Excessive accumulation of Ca
2+ in cytoplasm and mitochondria in hypoxia and subsequent reoxygenation can finally initiate cell injury and death via the opening of the Ca
2+-dependent mitochondrial permeability transition pore (MPT pore) and the subsequent release of proapoptotic proteins from organelles [
3].
As a major large-capacity buffer system of Ca
2+ ions, mitochondria are involved in the regulation of intracellular Ca
2+ homeostasis. Changes in mitochondrial [Ca
2+] modulate key cellular processes, ranging from aerobic metabolism (through Ca
2+-sensitive dehydrogenases, and enzymes of the Krebs cycle [
4]) to the release of proapoptotic factors [
5,
6,
7,
8], as well as local modulation of the activity of channels and enzymes [
9,
10].
In recent studies, it has been found that mitochondria contain several proteins involved in mitochondrial Ca
2+ uptake: mitochondrial Ca
2+ uniporter complex (MCUC), RaM (the rapid mode of Ca
2+ uptake), Letm1 (leucine zipper and EF-hand-containing transmembrane protein 1), mitochondrial ryanodine receptor type 1, and uncoupling proteins [
5,
11]. Among them, the MCUC is believed to be the main calcium transport system, which mediates the electrophoretic influx of the ion into mitochondria. This multiprotein complex is composed of the pore-forming and calcium-conducting subunit MCU (mitochondrial calcium uniporter subunit), its paralogue MCUb (mitochondrial calcium uniporter dominant negative beta subunit), and regulatory subunits: the small membrane-spanning protein EMRE (essential MCU regulatory subunit), the peripheral membrane proteins acting as gatekeepers MICU1 and MICU2 (mitochondrial calcium uptake proteins 1 and 2), and MCUR1 (MCU regulator protein 1) [
5,
6]. Variations in the ratio of the subunits of MCUC determine the dynamics of mitochondrial Ca
2+ uptake in different tissues and pathophysiological states. For example, a decrease in the expression of MICU1 in the heart tissue correlates with the lowered activation threshold of Ca
2+ influx and the decreased calcium capacity of heart mitochondria in comparison with those of liver mitochondria [
12]. MCUb mRNA is highly expressed in the heart and minimally expressed in skeletal muscle, which can be the cause of variations in the tissue-dependent mitochondrial Ca
2+ uptake: the Ca
2+ influx into skeletal muscle mitochondria is significantly greater than that into cardiac ones [
13].
Excessive accumulation of Ca
2+ in mitochondria leads to the opening of the Ca
2+-dependent mitochondrial permeability transition pore (MPT pore), which can be a key step in the mechanism of the activation of programmed cell death or, under certain conditions, can serve as an additional nonspecific calcium release pathway. The molecular structure of the MPT pore is as yet not clearly established. The MPT pore complex is considered to be a multiprotein mega-channel, which includes proteins of the inner and outer mitochondrial membranes. Among possible candidates for the role of the channel-forming subunit of the MPT pore are considered a number of proteins of the inner mitochondrial membrane, including ATP synthase, adenine nucleotide translocator, and phosphate carrier. At the same time, the only protein that is currently claimed to be an integral part of the MPT pore is the regulatory protein cyclophilin D, which is able to interact with the above-mentioned proteins. Cyclophilin D is the target of the cyclic undecapeptide cyclosporin A (CsA), which desensitizes the MPT pore complex to calcium ions at nanomolar concentrations [
5,
14].
Studies on the role of mitochondrial Ca
2+ transport systems in the pathogenesis of hypoxia have been ongoing for a long time. It was found that the pharmacological or genetic modulation of cyclophilin D leads to the inhibition of pore opening in mitochondria and increases the resistance of cell cultures and tissues to the hypoxic state. At the same time, the question of how the structure and operation of the mitochondrial Ca
2+ transport system and the MPT pore can be regulated in hypoxia and hypoxic adaptation remains unclear. The answer to this question should be found when conducting studies on animals with different individual resistance to acute hypoxia [
15,
16,
17]. It is known that the onset and severity of the acute hypoxia response of rats drastically differ within the population, and two opposite, extreme phenotypes of animals, with high resistance (HR) and low resistance (LR) to hypoxia, have significantly different “functional-metabolic profiles” [
18]. Thus, we have shown earlier that the liver mitochondria of HR and LR rats have different resistance to the formation of Ca
2+-dependent mitochondrial pores of two types, the MPT pore and the lipid pore induced by saturated long-chain fatty acids [
19].
In the present work, we attempted to determine the structural and functional features of the mitochondrial Ca2+ transport multiprotein systems, the MCUC and the MPT pore, in liver and heart tissues of animals with different tolerance to oxygen shortage. The study demonstrates that: (1) the rate of accumulation of Ca2+ ions by mitochondria isolated from the liver and heart of HR rats is considerably higher than that of LR rats, which highly correlates changes observed in the content, the ratio, and mRNA level of the subunits of the MCUC. In HR rats, the levels of the pore-forming uniporter subunit, MCU, and the key regulatory uniporter subunit, MICU1, in liver mitochondria are significantly higher than in LR rats. The level of the dominant-negative channel subunit, MCUb, is lower in heart mitochondria of HR rats compared to those of LR rats; (2) the liver mitochondria of HR animals are more resistant to the induction of the MPT pore than those of LR animals. This difference can be associated with the lower level of ATP synthase, a protein considered to be the channel-forming component of the MPT pore, in liver tissue of HR animals. In heart mitochondria of rats of the two phenotypes, no difference in the formation of MPT pore was revealed.
2. Materials and Methods
2.1. Testing the Tolerance of Rats to Extreme Hypoxia Conditions
Experiments were conducted on Wistar male rats (220–250 g) with different baseline resistance to hypoxia, low-resistance (LR) and high-resistance (HR) rats. The resistance of rats was tested one month prior to the experiments using a special procedure [
19]. Animals were placed into a hypoxic chamber and then tested for the ability to endure a critical life-incompatible O
2 concentration. For this test, the concentration of oxygen in the chamber was reduced to 3.1% by its displacement with nitrogen gas, and the time of the onset of pathological breathing (apnea) (T
a) was determined. This parameter characterizes the viability of animals under extreme hypoxic conditions and reflects the ability to fully mobilize the nonspecific protective functions responsible for the survival of the organism in the sublethal period. After registering T
a, the hypoxic chamber was opened, and the normal posture and locomotor activity of the animals restored within 5–10 min. The T
a value was 1–2 min for LR rats and more than 10 min for HR rats. Each group of rats amounted to approximately 20% of the total number of animals tested (n = 30). An interval of one month after the procedure of testing the tolerance of rats to hypoxia conditions was chosen on the basis of earlier studies to eliminate the effect of hypoxic exposure and to identify the basal differences between two rat phenotypes [
15,
16,
18]. After this interval, two extreme types of animals with different tolerance to acute oxygen deficiency exhibit characteristic features of the ultrastructure and functional activity of mitochondria of different organs [
16,
19].
The laboratory animals were treated in accordance with the European Convention for the Protection of Vertebrates used for experimental and other purposes (Strasbourg, 1986) and the principles of the Helsinki Declaration (2000). All the protocols were approved by the Institute of Theoretical and Experimental Biophysics RAS Ethics Committee (Order No. 173/k of 03.10.2011, Protocol No. 03/2019 of 05.03.2019).
2.2. Isolation of Rat Liver and Heart Mitochondria
Mitochondria were isolated from the liver and heart of Wistar rats by differential centrifugation as described earlier [
19]. The homogenization buffer contained 210 mM mannitol, 70 mM sucrose, 1 mM EDTA, and 10 mM Hepes/KOH buffer, pH 7.4. Subsequent centrifugations were performed in the same buffer, except that, instead of EDTA, 100 μM EGTA was used. Final suspensions contained 70–80 mg of mitochondrial protein/mL and 25–35 mg of mitochondrial protein/mL (liver and heart mitochondria, respectively), as determined by the Lowry method [
20].
2.3. Ca2+ Uptake by Mitochondria
The Ca2+ concentration in the incubation medium was monitored spectrophotometrically with an arsenazo III indicator at 675–685 nm using a plate reader Tecan Spark 10M (Tecan, Männedorf, Switzerland) at 25 °C under constant stirring. At a neutral pH, Ca2+ forms a complex with arsenazo III, which has a blue color. The color intensity is proportional to the concentration of Ca2+ in a buffer and can be measured spectrophotometrically. Mitochondria (0.4–0.5 mg of mitochondrial protein/mL) were suspended in an incubation medium containing 210 mM mannitol, 70 mM sucrose, 1 mM KH2PO4, 50 μM arsenazo III, 10 μM EGTA, and 10 mM HEPES-KOH (pH 7.4) and energized with 2.5 mM glutamate + 2.5 mM malate. After the addition of 50 μM CaCl2, the rate of Ca2+ uptake by mitochondria (nmol Ca2+ × min−1 × mg−1 of mitochondrial protein) was determined in the presence of 1 μM CsA. To determine the ability of mitochondria to retain Ca2+, 10 μM CaCl2 was added into the reaction medium successively, with an interval of ~90 s. After several additions, external [Ca2+] increased, indicating a massive release of the ion from the organelles due to the opening of the MPT pore. The amount of Ca2+ released upon permeability transition (defined as Ca2+ retention capacity) was used as a measure of the MPT pore opening probability.
2.4. Electrophoresis and Immunoblotting of Mitochondrial Proteins
To prepare samples for quantifying the levels of mitochondrial proteins, aliquots of native mitochondria (2 mg/mL) were solubilized in Laemmli buffer in Eppendorf tubes and heated for 3 min at 95 °C. Sample aliquots normalized by the protein concentration (10 µg of mitochondrial protein) were applied to the lanes and subjected to electrophoresis followed by Western blot analysis. Mitochondrial samples were separated by 12.5% SDS-PAGE and transferred to a 0.45 µm nitrocellulose membrane (Amersham, Munich, Germany). The proteins of PageRuler Prestained Protein Ladder (Thermo Scientific, Waltham, MA USA) were used as markers. After overnight blocking, the membrane was incubated with the appropriate primary antibody. The monoclonal rabbit anti-MCU (#14997), anti-CBARA/MICU1 (#12524), and anti-ANT2/SLC25A5 (#14671) antibodies were from Cell Signaling Technology Inc. (Danvers, MA, USA). The total OXPHOS Rodent WB Antibody Cocktail (#ab110413) containing the α-subunit of complex V (CV-ATP5A-55 kDa), anti-VDAC1 (#ab154856), and the polyclonal rabbit antibodies Anti-CCDC109B (#ab170715), anti-cyclophilin F (CypD) (#ab64935), and anti-ANT1 (#ab102032) were from Abcam (Cambridge, United Kingdom). The immunoreactivity was detected using the appropriate secondary antibody conjugated to horseradish peroxidase (#7074, Cell Signaling Technology Inc., Danvers, MA, USA). Peroxidase activity was detected with ECL chemiluminescence reagents (Pierce, Rockford, IL, USA). The relative levels of the detected proteins were visualized using an LI-COR system (LI-COR, Lincoln, NE, USA). Optical density measurements were performed using the LI-COR Image Studio software.
2.5. RNA Extraction, Reverse Transcription, and Quantitative Real-Time PCR
Total RNA was isolated from 100 mg of deep-frozen tissue samples (the liver or the heart) using an ExtractRNA kit (Eurogen, Moscow, Russia) in accordance with the protocol of the manufacturer. The resulting RNA preparation was treated with RNase-free DNase I (Thermo Scientific, Waltham, MA USA). The concentration of total RNA was measured spectrophotometrically using a Nanodrop ND-1000 spectrophotometer (ND Technologies, Fremont, CA, USA). Two micrograms of total RNA was taken for cDNA synthesis; reverse transcription was performed using an oligo(dT)15 primer and MMLV reverse transcriptase (Eurogen, Moscow, Russia) according to the manufacturer’s instructions. Real-time PCR was performed using a DTLite5 amplifier (DNA-Technology LLC, Moscow, Russia) using the qPCRmix-HS SYBR reaction mixture (Eurogen, Moscow, Russia). The selection and analysis of gene-specific primers were performed using Primer-BLAST [
21] (the oligonucleotide sequences are presented below; see
Table 1). The relative level of the expression of each gene was normalized by the level of mRNA of the cytoskeletal protein beta-actin (Actb), and a comparative C
T method was used to quantify the results [
22].
2.6. Statistical Analysis
The data were analyzed using the GraphPad Prism 7 and Excel software and presented as mean (median) ± SEM of 3–5 experiments. Statistical differences between the means were determined by Mann–Whitney U test; p < 0.05 was considered to be statistically significant.
4. Discussion
It is generally accepted that mitochondria are one of the main intracellular targets of hypoxia. Structural, biochemical, and functional abnormalities of mitochondria are widely believed to be important pathogenetic factors that underlie hypoxic or ischemic cell injury [
1,
18]. Apart from disordering mitochondrial ATP synthesis, network dynamics, and redox state, hypoxia also dysregulates the Ca
2+ homeostasis of these organelles and the cell as a whole. The hypoxia-induced dramatic alterations in Ca
2+ transport in mitochondria may not only be related to the decreased oxidative phosphorylation (OXPHOS), a metabolic shift toward glycolysis, and the development of oxidative stress, but also induce cell death pathways via mitochondrial Ca
2+ overload and the formation of Ca
2+-dependent MPT pore in the inner mitochondrial membrane, leading to the release of proapoptotic proteins into the cytosol [
3]. Consequently, it has been proposed that mitochondrial Ca
2+ transport pathways might be targets for protective intervention, as well as involved in the formation of the molecular mechanism of cell resistance to hypoxia and ischemia. The purpose of our work was to study in more detail the features of structure and operation of the Ca
2+ transport systems in the mitochondria of the liver and heart of rats with originally different tolerance to acute hypoxia.
The results obtained in this work indicate that mitochondria of HR and LR rats are characterized by fundamentally different genetically programmed rearrangements of the systems regulating Ca
2+ homeostasis. In the case of HR rats, the rearrangements of the Ca
2+ uniporter can increase the efficiency of Ca
2+ accumulation by liver and heart mitochondria. At the same time, the organelles of the liver of HR rats become more resistant to the opening of the Ca
2+-dependent MPT pore in comparison with those of LR rats. Along with the well-characterized distinction in the intensity of OXPHOS in mitochondria of the vital organs of LR and HR rats [
18,
25], these effects might contribute to the development of individual systemic resistance of animals to acute hypoxia.
It is well known that individuals of an animal population differ in their tolerance to oxygen deficiency [
15,
16,
17,
25]. As shown earlier, animals that belong to two opposite, in regard to hypoxia tolerance, types (LR and HR) have essentially different “functional-metabolic” profiles, including the effectiveness of energy support of the organism, the regulation of central nervous cardiovascular systems, neurohumoral regulation, stress-activating and stress-limiting systems, the oxygen-transporting function of blood, and the state of membranes and receptors. LR animals are considered to have a weak type of the nervous system, increased excitability, and emotional reactivity. LR animals respond to hypoxia with agitation and high locomotor activity. In contrast, HR animals have reduced excitability and anxiety, milder aggressiveness, more pronounced internal inhibition, low sensitivity to any provocative factors, and a tendency to social domination [
18].
It was previously shown that mitochondria of the vital organs of LR and HR rats differ in both structural and basic functional parameters. Thus, the mitochondria of the cerebral cortex of HR rats are characterized by a denser packing of cristae and a more electron-dense matrix, smaller sizes, and higher concentrations of the respiratory chain complexes and the respiration substrate, succinate (i.e., they are functionally more active compared to mitochondria of LR rats) [
16,
25]. In contrast, in brain mitochondria of LR rats, the number of mitochondrial cristae is decreased, and this is consistent with the lower content of their respiratory electron carriers compared to mitochondria of HR rats. It was also found that in liver mitochondria of HR animals, the rate of the ATP-dependent potassium transport, which reflects the activity of the mitochondrial ATP-sensitive potassium channel, was increased [
17].
Here, we have demonstrated that, in addition to the above structural–functional features, the mitochondria of the liver and heart of rats with originally different tolerance to hypoxia are distinguished in respect to the rate of influx of Ca2+ ions via MCUC. The liver and heart mitochondria of HR rats are characterized by a significant increase in the efficiency of Ca2+ uniport compared to the organelles of LR rats, with the difference being especially pronounced for the liver tissue. To elucidate the causes of these functional effects, we have examined structural changes in the Ca2+ transport system of mitochondria of LR and HR rats and revealed that these changes do occur in the macromolecular complex of the mitochondrial Ca2+ uniporter in the heart and liver tissues.
The MCUC is considered to consist of two transmembrane channel subunits: MCU and MCUb. MCU forms a highly selective Ca
2+ channel, which transfers the ion across the inner mitochondrial membrane. MCUb is a dominant-negative MCU paralogue, and its overexpression impairs the ion-transporting function of the complex [
13]. MCU and MCUb are associated with other subunits: MICU1-2, EMRE, and MCUR1, which act as regulators of the uniporter.
As follows from the data obtained, in HR animals, the contents of the pore-forming subunit MCU and the gate subunit MICU1 are substantially increased in liver mitochondria, whereas the level of the dominant-negative subunit, MCUb, is decreased in heart mitochondria. The data are confirmed by the results of real-time PCR analysis and indicate that these changes occur at the level of transcription. At the same time, there is almost no difference between liver and heart mitochondria of LR and HR animals in the content of the regulatory uniporter subunit EMRE and the expression of its gene.
It is known that the activity of MCUC is regulated by changes in the ratio of the Ca
2+-conducting pore subunits MCU and MCUb [
5,
26,
27]. Therefore, both an increase in the level of MCU and a decrease in the content of its paralogue MCUb, which we recorded in mitochondria of the liver and heart of HR animals, can be the cause of the increased rate of Ca
2+ influx into the organelles. Based on the data obtained, we can conclude that the structural changes in the pore-forming subunits of MCUC in HR rats increase the efficiency of Ca
2+ accumulation in the mitochondrial matrix and, as a result, might underlie the fine control of cytoplasmic free Ca
2+ at low levels.
On the other hand, excessive accumulation of Ca
2+ into mitochondria can result in the opening of MPT in the inner mitochondrial membrane. As a result, all transmembrane ionic gradients and the membrane potential collapse, and mitochondria swell, which leads to the rupture of their outer membrane and the release of proapoptotic proteins (cytochrome
c, apoptosis-inducing factor, and others) from the organelles. This can facilitate the activation of the caspase cascade, DNA damage, and eventually cell death. The opening of the MPT pore is believed to be triggered by hypoxia and subsequent reoxygenation [
3,
14]. The data obtained in this work show that liver (but not heart) mitochondria of HR rats have a significantly higher Ca
2+ capacity (i.e., are more resistant to the induction of the MPT pore than the organelles of LR rats). Similar results were partially obtained by us earlier [
19]. In order to gain insight into the molecular mechanism of tolerance of liver mitochondria of HR rats to MPT, we assayed for levels of MPT-associated mitochondrial proteins: cyclophilin D, ATP synthase (α-subunit), and adenylate translocator ANT1 (
Figure 4). Our results indicate that the levels of cyclophilin D and ANT1 in mitochondria of the liver of HR and LR rats are not distinguished. There is, however, a significant decrease in the content of the α-subunit of ATP synthase (a protein that supposedly forms the channel of the MPT pore) in liver mitochondria of HR rats. Thus, the increased tolerance of liver mitochondria of HR rats to MPT, as compared with mitochondria of LR rats, can be related to a lowered expression of the MPT pore-forming protein. This is in agreement with the earlier report that the changes in expression of ATP synthase had significant effects on the probability of MPT induction [
28].
However, the question as to which subunit of this multisubunit complex is the central structural component of the MPT pore, or whether it is formed by MPT-specific conformation of dimers of ATP synthase, remains the province of further investigations.
It should be noted that the CRC index of mitochondria isolated from the heart of HR rats was slightly lower compared to that of LR rats, although this difference was not statistically significant. This trend toward a decline in the Ca
2+ buffering capacity is likely explained by the fact that the content of cyclophilin D, a major regulatory protein of the MPT pore [
14,
29,
30], in heart mitochondria of HR rats is increased (
Figure 6). It is believed that VDAC1 is also involved in the formation of the MPT pore complex in mitochondria. In addition, this protein participates in the formation of MAM contacts, which are the main pathway of Ca
2+ transfer from the endoplasmic reticulum to mitochondria [
5,
14]. So, the changes observed in the level of VDAC1 can also contribute to the tissue-specific modulation of mitochondrial Ca
2+ handling and the MTP opening.
Based on the results obtained, one can assume that the increase in the rate of Ca2+ transport in mitochondria is not accompanied by a higher susceptibility of mitochondria to calcium overload and the induction of the MPT pore. As follows from our data, changes in the levels of the MPT-related proteins can play a crucial role in the regulation of pore formation in mitochondria. At the same time, the high rate of mitochondrial Ca2+ uptake may provide a more effective removal of excess Ca2+ ions from the cytosol under physiological conditions and hypoxia.