- Research article
- Open Access
Release of Ca2+ and Mg2+ from yeast mitochondria is stimulated by increased ionic strength
© Bradshaw and Pfeiffer; licensee BioMed Central Ltd. 2006
- Received: 03 November 2005
- Accepted: 06 February 2006
- Published: 06 February 2006
Divalent cations are required for many essential functions of mitochondrial metabolism. Yet the transporters that mediate the flux of these molecules into and out of the mitochondrion remain largely unknown. Previous studies in yeast have led to the molecular identification of a component of the major mitochondrial electrophoretic Mg2+ uptake system in this organism as well as a functional mammalian homolog. Other yeast mitochondrial studies have led to the characterization of an equilibrative fatty acid-stimulated Ca2+ transport activity. To gain a deeper understanding of the regulation of mitochondrial divalent cation levels we further characterized the efflux of Ca2+ and Mg2+ from yeast mitochondria.
When isolated mitochondria from the yeast Saccharomyces cerevisiae were suspended in a salt-based suspension medium, Ca2+ and Mg2+ were released from the matrix space. Release did not spontaneously occur in a non-ionic mannitol media. When energized mitochondria were suspended in a mannitol medium in the presence of Ca2+ they were able to accumulate Ca2+ by the addition of the electrogenic Ca2+ ionophore ETH-129. However, in a KCl or choline Cl medium under the same conditions, they were unable to retain the Ca2+ that was taken up due to the activation of the Ca2+ efflux pathway, although a substantial membrane potential driving Ca2+ uptake was maintained. This Ca2+ efflux was independent of fatty acids, which have previously been shown to activate Ca2+ transport. Endogenous mitochondrial Mg2+ was also released when mitochondria were suspended in an ionic medium, but was retained in mitochondria upon fatty acid addition. When suspended in a mannitol medium, metal chelators released mitochondrial Mg2+, supporting the existence of an external divalent cation-binding site regulating release. Matrix space Mg2+ was also slowly released from mitochondria by the addition of Ca2+, respiratory substrates, increasing pH, or the nucleotides ATP, ADP, GTP, and ATP-gamma-S.
In isolated yeast mitochondria Ca2+ and Mg2+ release was activated by increased ionic strength. Free nucleotides, metal ion chelators, and increased pH also stimulated release. In yeast cells this release is likely an important mechanism in the regulation of mitochondrial matrix space divalent cation concentrations.
- Divalent Cation
- Matrix Space
- Ionic Medium
- Yeast Mitochondrion
- Mammalian Mitochondrion
Mg2+ is the most abundant divalent cation in cells and is important for many metabolic processes. Free Mg2+ in cells is quite low (0.3 – 3%) as compared to the total amount of Mg2+ due to buffering by polyphosphates, nucleic acids, and free nucleotides [1, 2]. In mammalian cells the free concentration is usually maintained at a concentration between 0.25 and 1 mM . The Mg2+ level in the cell varies during changing physiological conditions. The free Mg2+ level increases slightly as ATP levels decrease. The total cellular Mg2+ level changes upon the addition of several hormones to cells . Recently the TRPM family of ion channels has been found to play an important role in cellular Mg2+ homeostasis in several tissues . This suggests that regulated pathways for Mg2+ transport exist to maintain proper intracellular levels.
Mammalian mitochondrial Mg2+ transport
The pathways involved in mammalian mitochondrial Mg2+ flux are largely unknown. The human homolog of a component of the main electrophoretic mitochondrial Mg2+ transporter in yeast has been cloned . The protein can functionally substitute for its yeast homolog. These double membrane-spanning proteins likely homo-oligomerize to form ion-transporting complexes. However definitive evidence that this protein functions in mammalian mitochondrial ion transport has yet to be obtained.
Heart mitochondria take up and release Mg2+ in a respiration-dependent manner [6–8]. Uncouplers of respiration that dissipate the membrane potential release mitochondrial Mg2+ into the cytoplasm . There is evidence that hormones alter mitochondrial Mg2+ levels . Hormones may increase cyclic AMP (cAMP) levels to stimulate Mg2+ transport . Fatty acids have been shown to stimulate the efflux of mitochondrial Mg2+ at alkaline pH . Even though mitochondrial Mg2+ has been well characterized at the isolated organelle level, the cellular signals regulating mitochondrial Mg2+ transport have not been clearly elucidated.
Mg2+ transport in yeast
In yeast cells when medium Mg2+ is plentiful (> 1 mM), yeast cells contain around 400 nmole Mg2+/mg protein . As medium Mg2+ decreased (0.02 mM), cellular Mg2+ decreased to levels near 80 nmole/mg protein. In times of ample Mg2+, the Mg2+ is taken up and stored in the vacuole. When these cells were then placed in a Mg2+ free growth medium, they survived by utilizing their vacuole stores. But once the cellular Mg2+ level became too low, the yeast cells died, in contrast to limitations in many other nutrients in which the cells survive in the G0 phase of the cell cycle .
Two genes comprising the yeast Mg2+ uptake system in the plasma membrane have been identified . Yeast plasma membrane Mg2+ transport is inhibited by aluminum  and polyamines . Since overexpression of either of the Mg2+ transport proteins confers resistance to aluminum toxicity, the inhibition of Mg2+ uptake may be the primary cause for aluminum toxicity in yeast . Mg2+ may also provide benefits to cells confronted with heavy metals. Increased cellular Mg2+ levels protected cells from toxic concentrations of Mn2+ by down-regulating Mn2+ transport .
Yeast mitochondrial Mg2+
Mg2+ is essential for many mitochondrial reactions including those of DNA and RNA metabolism [16, 17] as well as ATP synthesis . Mg2+ blocks the yeast mitochondrial ATP-induced unspecific channel (YMUC) . Mg2+ also inhibits mitochondrial anion uniport . Therefore, the regulation of matrix space Mg2+ could be important for the mitochondrial distribution of many other ions. In this report we discovered that Mg2+ and Ca2+ are released from yeast mitochondria under conditions of increased ionic strength. In yeast cells this release pathway is likely an important regulator of mitochondrial divalent cation levels.
Ionic media prevent ETH-129-mediated accumulation of mitochondrial Ca2+
In the KCl medium in the absence of Ca2+ and ETH-129, the ΔΨ was roughly twenty percent smaller than that observed when the mitochondria were suspended in a mannitol medium. Immediately following Ca2+ and ETH-129 addition the ΔΨ in the mannitol medium dropped to a lower value than that observed after the same treatment in the KCl medium. At the same time Ca2+ was taken up more rapidly in the mannitol medium. Therefore a sufficient driving force for mitochondrial Ca2+ uptake by ETH-129 was maintained in the KCl medium although the Ca2+ was not retained in the organelle. The steady state ΔΨ attained in the 0.3 M KCl media after Ca2+ and ETH-129 addition was approximately two-thirds of the value of that in the mannitol medium. These results are consistent with the activation of a Ca2+/H+ exchange when mitochondria are suspended in the ionic media. This activity together with the electrogenic ETH-129-mediated Ca2+ uptake causes proton re-entry into the matrix space to slightly decrease the ΔΨ. After the ΔΨ reached a steady state, it was completely dissipated by addition of the uncoupler FCCP (carbonyl cyanidep-trifluoromethoxyphenylhydrazone) to give the baseline level.
In a previous report a large decrease in the ΔΨ occured after ETH-129 addition to mitochondria suspended in a mannitol medium in the absence of BSA (bovine serum albumin) . Together with ionophore-catalyzed Ca2+ influx, activation of a fatty acid stimulated Ca2+/H+ exchange led to the decreased ΔΨ. Because the ΔΨ was not dissipated to as great of an extent when mitochondria were suspended in a KCl medium, the Ca2+ efflux pathway described here appears to be less active than the one activated by fatty acids .
Increasing ionic strength induces release of Mg2+ from mitochondria
Mg2+ was also released from the matrix space when mitochondria were suspended in all other ionic media tested including K+ TES, NaCl, and tetramethylammonium (TMA) Cl (data not shown). Endogenous Mg2+ was released from the matrix space at slightly different rates in the different ionic media in increasing order TMA Cl < choline Cl < KCl < Tris Cl (compare K+ in Figure 3A to choline in Figure 3B). These rates of Mg2+ release corresponded to the rates of spontaneous swelling of yeast mitochondria in these salt media. However, Mg2+ was released even faster than any of these spontaneous rates in a KCl medium in the presence of 1 mM ethanol (data not shown) where no swelling occurred (see Figure 2A). Mg2+ was also released at a substantial rate in K+ TES media where no swelling occurred. Therefore organelle lysis due to matrix space swelling was not responsible for the Mg2+ release. The entry of ions into the matrix space may help displace bound Mg2+ to stimulate the rate of efflux.
When non-energized yeast mitochondria were suspended in a choline Cl medium, the addition of either EDTA (ethylenediaminetetraacetic acid) or ADP slightly increased the Mg2+ efflux rate (Figure 3B). The combined presence of EDTA and ADP increased the rate of Mg2+ efflux more than either compound alone. The addition of ethanol as a respiratory substrate also increased the efflux of Mg2+. Since ethanol opens the yeast mitochondrial unselective channel (YMUC), decavanadate, a YMUC inhibitor [27, 28], was present in the medium during all experiments. Since the efflux of Mg2+ is fairly rapid even in the absence of ADP, EDTA, or ethanol, the addition of these compounds only slightly stimulated the rate of efflux.
EDTA, respiration, ADP, and ATP stimulate loss of Mg2+ from mitochondria
Effectors of yeast mitochondrial Mg2+ release. Yeast mitochondria were suspended in 0.6 M mannitol, 10 mM HEPES (TEA+), pH 7.20, and 0.1 mM decavanadate (Na+). Mitochondrial Mg2+ was measured at 20 minutes. The percentage of Mg2+ released was compared to that released in the presence 2 mM ATP (Na+).
% of 2 mM ATP induced Mg 2+ release
2 mM GTP
2 mM ATP gamma-S
2 mM ADP
2 mM AMP
0.2 mM cyclic AMP
2 mM FSBA
2 mM ADP + 2 mM FSBA
0.1 mM Ca2+
0.1 mM EGTA
0.1 mM EDTA
Fatty acids do not stimulate mitochondrial Mg2+ efflux
Increasing pH stimulates mitochondrial Mg2+ efflux
Mitochondrial divalent cation influx
The present study describes conditions in which isolated yeast mitochondria are able to release Mg2+ and Ca2+ from the matrix space. The efflux is most active when mitochondria are suspended in a high ionic strength medium. Respiration, ATP, ADP, EDTA, and Ca2+ are also able to stimulate Mg2+ efflux.
The essential role of Mg2+ in mitochondrial metabolism
Genetic studies in yeast have established that Mg2+ is essential for mitochondrial RNA metabolism . Mg2+ also regulates the yeast mitochondrial ATP synthase . The free concentration of Mg2+ in beef heart mitochondria is estimated to be between 0.7 and 0.9 mM . Within the physiological range, Mg2+ can modulate the efficiency of the mammalian 2-oxoglutarate dehydrogenase and mitochondrial ATP synthase to affect the rate of oxidative phosphorylation . Therefore the matrix space Mg2+ level needs to be maintained within a specific range to maintain proper mitochondrial function. However in other species and tissues mitochondrial Mg2+ has been shown to vary over a larger range from 0.2 to 1.5 mM [32, 33].
The role of EDTA and EGTA in stimulating Mg2+ efflux
EDTA and EGTA have very different affinities for activating mitochondrial Mg2+ release. The most likely candidate for a metal ion bound by EDTA and EGTA to activate Mg2+ release is Mg2+ itself because it has a greatly different affinity for each of these chelators. Many other divalent cations such as Ca2+ do not satisfy this criterion. The ability of EDTA to activate mitochondrial Mg2+ efflux from the cytoplasmic side of the inner membrane suggests that when the cytoplasmic concentration of the inhibiting ion is low, mitochondrial Mg2+ equilibrates with the cytoplasmic concentration. However, the significance of mitochondrial Mg2+ efflux functioning to supply Mg2+ to the cytoplasm is questionable, since the vacuole is the major storage organelle for Mg2+ in yeast cells .
The presence of a cytoplasmically facing Mg2+ inhibiting the mitochondrial efflux of divalent cations does not appear to be entirely consistent with a mitochondrial influx of Mg2+ (see Figure 8). Binding of Mg2+ to the external inhibitory site may be expected to inhibit Mg2+ influx into the matrix space. However, a salt-based medium may displace inhibitory Mg2+. Yeast mitochondria do not swell when suspended in a 0.3 M Mg2+ acetate medium  indicating that an influx of Mg2+ into the matrix space does not occur at this very high concentration. Therefore mitochondrial influx may depend on the specific KCl and Mg2+ concentrations employed. In a previous report Mg2+ was transported into yeast mitochondria in the absence of a membrane potential, however at a highly reduced rate compared to energized mitochondria .
Comparison to yeast mitochondrial cation transporters
Fatty acids and BSA do not regulate the mitochondrial Mg2+ and Ca2+ release studied in this report as they did the yeast mitochondrial fatty acid-induced Ca2+/H+ exchanger described previously . Since yeast mitochondria in situ are exposed to an environment containing KCl and do not appear to have a high activity Ca2+ efflux pathway open , perhaps some regulatory element inhibiting mitochondrial Ca2+ release is lost during mitochondrial isolation or upon suspension of isolated mitochondria in ionic media.
The yeast mitochondrial Mg2+ release activity may be of a similar nature as the yeast mitochondrial K+/H+ exchange. The similar inhibitors and conditions stimulating mammalian mitochondrial K+ and Mg2+ transport have been noted previously [12, 34]. The activities of both yeast proteins are non-specific in nature  (and see Figure 8). Cations also stimulate both activities  (and see Figure 6). Further experiments are needed to determine if divalent cations can exchange for many other cations across the inner mitochondrial membrane or just for protons. Both yeast mitochondrial Mg2+ release and K+/H+ exchange appear to be inhibited by divalent cations. The yeast K+/H+ exchange, although only moderately inhibited by Mg2+, is strongly inhibited by Zn2+ [26, 35, 36], whereas the ability of chelators to activate Mg2+ release suggests a role for divalent cations in regulating this activity as well. However there is at least one striking difference in the regulation of yeast mitochondrial Mg2+ release and K+/H+ exchange. The K+/H+ exchange appears to be spontaneously active in isolated yeast mitochondria  when they are suspended in a mannitol medium as monitored by the efflux of endogenous K+ (data not shown) while Mg2+ release does not occur spontaneously in a mannitol medium.
In a previous study no loss of free mitochondrial Mg2+ was detected in yeast mitochondria when they were suspended in a 0.135 M KCl medium for thirty minutes , while we detect a loss of over 70 percent of the total mitochondrial Mg2+ levels in just ten minutes in 0.3 M KCl media using mitochondria from strain W303-1A. However, in the previous study the DBY747 yeast strain was used and the mitochondria were preloaded in a 10 mM Mg2+ 135 mM KCl medium before Mg2+ release was monitored. It will be important to determine which of these factors is responsible for the different Mg2+ efflux results.
Yeast mitochondrial Mg2+ efflux candidates
Mitochondrial matrix space Mg2+ is important for many aspects of nucleotide metabolism [37, 38]. Two inner mitochondrial membrane transporters, Mrs2p and Lpe10p, are needed for group II intron splicing [16, 39]. MRS2 and LPE10 have slight sequence similarity with the bacterial Mg2+transporter CorA. Assays with a fluorescent Mg2+ indicator dye indicate that Mrs2p is part of an electrophoretic mitochondrial Mg2+ influx pathway inhibited by cobalt(III)hexaammine . Mitochondrial Mg2+ levels changed with the levels of Mrs2p and Lpe10p. Mitochondrial electrophoretic Mg2+ uptake was absent in an MRS2 deletion strain. Mrs2p and Lpe10p are essential for yeast growth on nonfermentable carbon sources . However they cannot substitute for each other suggesting non-redundant functions. It is possible that Mrs2p or Lpe10p is responsible for the mitochondrial Mg2+ release described in this report. However, in the previous experiments Mg2+ was taken up by energized mitochondria in an Mrs2p-dependent manner where we found that Mg2+ was released from energized mitochondria . In the previous study there was also no difference in the uptake of Mg2+ in ionic or non-ionic media, while greatly differing Mg2+ efflux results occurred in this report under these conditions. In addition cobalt(III)hexaammine, an inhibitor of Mrs2p, blocked Mg2+ transport while having no effect on Ca2+ transport , while the efflux described here appears not to discriminate between Mg2+ and Ca2+.
The YOL027 and YPR125 genes are multicopy suppressors of the respiratory-deficient phenotype caused by deletion of MRS2  and are therefore candidate mitochondrial Mg2+ transporters. YOL027p has been demonstrated to mediate K+/H+ exchange activity in yeast mitochondria . Because of the similarities in mitochondrial Mg2+ and K+ transport properties mentioned above either YOL027p or YPR125p may also function as a Mg2+/H+ exchanger. Mg2+ inhibited K+/H+ exchange activity in YOL027p-contaning submitochondrial particles. Deletion of YOL027 resulted in slightly altered mitochondrial transport rates of both Mg2+ and Ca2+ . It is possible that the homologous YPR125 gene (40 % sequence identity) could be responsible for the remaining Mg2+ and Ca2+ transport activity because overexpression of YPR125 rescued growth of the YOL027 deletion strain and YPR125p also localized to mitochondria.
When added to yeast cells certain ionophores such as nigericin selectively target mitochondria . Nigericin is an ionophore that possesses K+/H+ exchange activity. A screen for nigericin-resistant mutants revealed that the Mdm31 and Mdm32 genes may be involved in mitochondrial cation homeostasis . Mdm31 and Mdm32 deletion mutants contained a two to three-fold higher level of mitochondrial Mg2+ than the wild type. Since yeast mitochondrial K+/H+ exchange is inhibited by Mg2+ [36, 43], it was hypothesized that Mdm31p and Mdm32p may be proteins that mediate the efflux of mitochondrial Mg2+ . Knocking out their function could have elevated mitochondrial Mg2+ levels to inhibit the endogenous mitochondrial K+/H+ exchanger to rescue the cells from nigericin-mediated death.
Mammalian mitochondrial Mg2+ transport
We have shown that yeast mitochondria contain a Mg2+ release activity, while a similar activity has been demonstrated in mammalian mitochondria . Mammalian mitochondria are hypothesized to take up Mg2+ through a uniport mechanism or by respiration-dependent 'unspecific leak' and release Mg2+ by a Mg2+/H+ exchange [33, 44]. Our current data combined with data from the Schweyen laboratory  indicate that a similar system is likely present in yeast. They have characterized Mrs2 as the respiration-dependent mitochondrial Mg2+ uptake system, while the efflux described in this report is likely a Mg2+/H+ exchange. In this regard the respiratory substrate-induced release that occurs in yeast mitochondria in the absence of external Mg2+ resembles the respiration-induced release in rat heart attributed to Mg2+/H+ exchange . The ionic strength-induced release of Mg2+ in yeast mitochondria resembles a Mg2+ release activity in rat liver mitochondria that is stimulated by alkaline pH in the presence of fatty acids . This rat liver mitochondrial Mg2+ release also only occurred in an ionic medium. This suggests that yeast and mammalian mitochondrial Mg2+ transport may occur through similar mechanisms.
By using a Ca2+-indicating dye and measuring mitochondrial Mg2+ levels we have identified Ca2+ and Mg2+ efflux activities stimulated by increased ionic strength in yeast mitochondria. Mitochondrial efflux did not appear to be spontaneously active when isolated mitochondria were suspended in a sugar-containing medium. Nucleotide di- and tri- phosphates, increasing pH, and divalent cation chelators also activated mitochondrial Mg2+ release. The function of this mitochondrial efflux pathway is likely important for regulating the matrix space concentrations of Mg2+, Ca2+, and perhaps other divalent cations.
Yeast growth and mitochondrial isolation
The yeast strain W303-1A was grown aerobically at 30°C in a media containing 2% lactate, 1% yeast extract, 2% peptone, 0.05% dextrose, and 0.01% adenine at pH 5.0. Yeast cells were harvested during logarithmic growth phase (A600 = 1.8–2.2). Mitochondria were isolated from spheroplasts as previously described [21, 45], except 0.6 M sucrose was used in the homogenization buffer instead of 0.6 M mannitol. The isolated yeast mitochondria were suspended in 0.6 M mannitol, 20 mM HEPES (K+), and 0.1 mM EGTA, pH 6.8. Protein concentration was determined using a mini-Biuret method using BSA as a standard. Samples were solubilized in deoxycholate (Na+), which was present at a final concentration of 1% by weight.
For ion concentration determination atomic absorption spectrophotometry was performed using an AA-575 spectrophotometer (Varian). 2 mg of mitochondrial protein was incubated in the indicated media, spun down for 2 minutes in a microcentrifuge and the supernatant poured off. The mitochondrial pellet was solubilized with 0.6 mL 2 N perchlorate overnight. 0.5 mL was removed and diluted to 2 mL with deionized water prior to sample reading. For swelling experiments, solute permeability was monitored by light scattering using an SLM- Aminco DW-2C spectrophotometer in split beam mode at A540 using mitochondria suspended at 1 mg protein/ml. The uptake of Ca2+ by mitochondria was followed using antipyrylazo III as an indicator of the extramitochondrial Ca2+ concentration . Changes in ΔA720-A790 were recorded in the DW-2C operated in the dual wavelength mode and converted to Ca2+ concentration values using a calibration curve that was generated with a standard solution of Ca2+. Estimates of membrane potential were made using safranine O (12 μM) as an indicator. Safranine accumulation was followed spectrophotometrically, as a change in ΔA511-A533. Initial absorbances without mitochondria in the media were always set to identical values. After addition of mitochondria to the medium absorbances in different ionic strength media were shifted up or down compared to runs in the same media. However, the magnitude of the dye response was similar in the different ionic strength media. Therefore, the different runs were comparable after aligning their baseline membrane potentials after FCCP addition.
Free ion concentration determination
Medium free ion concentrations in the presence of chelators were determined using a computer program .
We would like to thank Dr. Dennis Jung for helpful discussions and Warren Erdahl for technical assistance. This research was supported by a grant from the NIH to DP (GM071396).
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