Intracellular diffusion restrictions in isolated cardiomyocytes from rainbow trout
© Sokolova et al; licensee BioMed Central Ltd. 2009
Received: 17 July 2009
Accepted: 17 December 2009
Published: 17 December 2009
Restriction of intracellular diffusion of adenine nucleotides has been studied intensively on adult rat cardiomyocytes. However, their cause and role in vivo is still uncertain. Intracellular membrane structures have been suggested to play a role. We therefore chose to study cardiomyocytes from rainbow trout (Oncorhynchus mykiss), which are thinner and have fewer intracellular membrane structures than adult rat cardiomyocytes. Previous studies suggest that trout permeabilized cardiac fibers also have diffusion restrictions. However, results from fibers may be affected by incomplete separation of the cells. This is avoided when studying permeabilized, isolated cardiomyocytes. The aim of this study was to verify the existence of diffusion restrictions in trout cardiomyocytes by comparing ADP-kinetics of mitochondrial respiration in permeabilized fibers, permeabilized cardiomyocytes and isolated mitochondria from rainbow trout heart. Experiments were performed at 10, 15 and 20°C in the absence and presence of creatine.
Trout cardiomyocytes hypercontracted in the solutions used for mammalian cardiomyocytes. We developed a new solution in which they retained their shape and showed stable steady state respiration rates throughout an experiment. The apparent ADP-affinity of permeabilized cardiomyocytes was different from that of fibers. It was higher, independent of temperature and not increased by creatine. However, it was still about ten times lower than in isolated mitochondria.
The differences between fibers and cardiomyocytes suggest that results from trout heart fibers were affected by incomplete separation of the cells. However, the lower ADP-affinity of cardiomyocytes compared to isolated mitochondria indicate that intracellular diffusion restrictions are still present in trout cardiomyocytes despite their lower density of intracellular membrane structures. The lack of a creatine effect indicates that trout heart lacks mitochondrial creatine kinase tightly coupled to respiration. This argues against diffusion restriction by the outer mitochondrial membrane. These results from rainbow trout cardiomyocytes resemble those from other low-performance hearts such as neonatal rat and rabbit hearts. Thus, it seems that metabolic regulation is related to cardiac performance, and it is likely that rainbow trout can be used as a model animal for further studies of the localization and role of diffusion restrictions in low-performance hearts.
In permeabilized preparations of mammalian oxidative muscles such as red skeletal muscle and the heart, diffusion of ADP and phosphate from the surrounding medium to the adenine nucleotide translocase (ANT) in the inner mitochondrial membrane is restricted [1, 2]. Especially the diffusion restriction of ADP in adult rat cardiomyocytes has received much attention, because the compromised energetic balance induced by ischemia-reperfusion damage is associated with diminished diffusion restrictions [3, 4].
The existence of diffusion restrictions is indicated by that the apparent ADP-affinity of mitochondria in situ in permeabilized fibers and cardiomyocytes is much lower (KM ADP~300 μM in rat fibers and cardiomyocytes) than the ADP-affinity of isolated mitochondria (KM ADP < 20 μM) [5–7]. It was first proposed that this was due to low permeability of the outer mitochondrial membrane, which is partially overcome by creatine kinase (CK) [8, 9]. In addition to the outer mitochondrial membrane, some diffusion restrictions also reside in the cytosol. They lead to a preferential metabolic channeling of ADP from ATPases to mitochondria . Likewise, ATP from mitochondria is channeled to the sarcoplasmic reticulum (SR) Ca2+-ATPase (SERCA) and myosin ATPase . This led to the hypothesis that cytosolic diffusion restrictions divide cardiomyocytes into subcellular compartments termed "intracellular energetic units" (ICEUs) [12–14]. Their confinement of ADP and ATP in small compartments with short diffusion distances enhances the functional coupling between adjacent energy producing mitochondria and energy consuming ATPases.
It is still not clear what causes the diffusion restrictions in rat cardiomyocytes. The importance of the outer mitochondrial membrane has recently regained attention in studies on isolated brain mitochondria suggesting that its permeability is regulated by tubulin [15, 16]. Possible candidates for cytosolic diffusion restrictions are membrane structures such as SR and t-tubules [12, 14]. But also cytoskeletal components such as tubulin have been proposed . These structures are rather densely packed in adult rat cardiomyocytes. In contrast, cardiomyocytes from rainbow trout (Oncorhynchus mykiss) have a relatively simple morphology. They are only 2-5 μm thick [17, 18], have no t-tubules and a sparsely developed SR . Below the sarcolemma is a single ring of myofilaments surrounding a central core of mitochondria [18, 20]. Thus, if t-tubules and SR cause diffusion restriction, we would expect diffusion restrictions to be much smaller in trout cardiomyocytes.
Previous studies on rainbow trout permeabilized cardiac fibers suggest that despite their simple morphology, they also have intracellular diffusion restrictions. As in rat permeabilized fibers, their apparent ADP-affinity is much lower than that expected for isolated mitochondria, but it is increased by the addition of creatine. Furthermore, a competitive assay with excess pyruvate kinase activity only partially inhibits mitochondrial respiration [21, 22]. However, the results from permeabilized fibers may be affected by incomplete cell separation, and/or clustering of fibers on top of the stirrer during oxygraphy measurements. These are avoided with permeabilized cardiomyocytes, since the single cells disperse evenly in the oxygraphy medium. Rat permeabilized fibers and cardiomyocytes have similar ADP-kinetics , which reaffirm the reliability of the results. However, trout permeabilized fibers have given contradictory results, because creatine lowers the apparent KM ADP [21, 23], but there does not seem to be a mitochondrial CK tightly coupled to respiration . The aim of this study was to control the existence of diffusion restrictions in trout cardiomyocytes by comparing the apparent ADP-affinity in permeabilized cardiac fibers, permeabilized isolated cardiomyocytes and isolated mitochondria. An effect of temperature on diffusion restrictions in terms of apparent KM ADP was found previously on both trout and rat cardiac fibers [23, 24]. This is important for the rainbow trout which lives at a temperature range of 2-23°C. Furthermore, due to the different temperature sensitivity of metabolism and diffusion speed, the effect of temperature allows us to draw conclusions about the importance of diffusion distance as one of the restricting factors. Therefore, the experiments were performed at 10, 15 and 20°C. Additionally, because CK may play an important role in facilitating ADP-diffusion across diffusion restriction barriers, the experiments were performed in both the absence and presence of creatine.
The experiments were complicated by hypercontraction of isolated trout cardiomyocytes in the R(respiration)-solution used previously for permeabilized fibers. This solution was originally developed for mammalian tissue and will be referred to as "mammalian R-solution". Therefore, we first had to develop a new "fish R-solution" for trout cardiomyocytes, in which they maintained shape and showed stable steady state respiration rates throughout each experiment. The results on cardiomyocytes were different from those on fibers suggesting that results from trout fibers were affected by incomplete separation of the cells. However, the apparent ADP-affinity of cardiomyocytes was still about an order of magnitude higher than that of isolated mitochondria. This indicates that trout cardiomyocytes still have diffusion restrictions despite their low density of intracellular membrane structures. However, in cardiomyocytes, creatine did not lower the apparent KM ADP suggesting that there is no mitochondrial creatine kinase tightly coupled to respiration to overcome diffusion restrictions.
Rainbow trout were obtained from local fish farms (Simuna Ivax OÜ, Lääne-Virumaa, and Forkala OÜ, Roosna-Alliku, Estonia). They were kept in a 1200 liter freshwater tank at 15 ± 1°C, and fed regularly with commercial fish food. They were allowed to acclimatize for at least 3 weeks before the experiments. All procedures were approved by the Estonian National Committee for Ethics in Animal Experimentation (Estonian Ministry of Agriculture). The fish was stunned by a single blow to the head followed immediately by a cut of the spine. The heart was excised and immediately transferred to ice-cold solution to minimize ischemia.
Preparation of permeabilized cardiac fibers
The excised heart was transferred to ice-cold isolation solution (see composition below). The ventricle was isolated and the spongy layer and compact layer were separated. The spongy tissue was cut into six smaller pieces, which were transferred to fresh S(skinning)-solution in a petri-dish on ice. Each piece was carefully dissected using fine tweezers (Dumont 3, Dumostar, World Precision Instruments) to separate the tissue into thin bundles of cells that were interconnected. The fibers were permeabilized by incubation for 30 min under continuous mixing in S-solution containing 50 μg/ml saponin at 4°C. After this, they were washed twice for 10 min in S-solution without saponin and stored at 4°C in S-solution until use within less than 3 hours.
Isolation of cardiomyocytes
The isolation of trout cardiomyocytes has been described previously . The heart was excised with atrium and bulbus arteriosus and transferred to ice-cold isolation solution (see composition below). A cannula was inserted through the bulbus arteriosus into the ventricle and the heart was perfused in retrograde manner with isolation solution for 8-10 min to wash the heart free from blood and to lower extracellular Ca2+-concentration. After washing, the heart was perfused with isolation solution containing 0.5 mg/ml trypsin, 0.75 mg/ml collagenase A and 0.75 mg/ml BSA for 18-20 min to digest the extracellular matrix and dissociate the cardiomyocytes. After digestion, the heart was taken off the cannula and cut into smaller pieces. The cardiomyocytes were suspended with a 1 ml pipette, where the tip had been cut off in order to minimize mechanical damage. The cell suspension was filtered through nylon tissue, and healthy cells were isolated by sedimentation. The isolation procedure was carried out at room temperature, and the isolated cells were kept in isolation solution at 4°C until use within at least 3 hours.
Isolation of mitochondria
Mitochondria were isolated by differential centrifugation of tissue homogenate similar to in Bouzidi et al. . The heart was excised and transferred to buffer A (see composition below). The atrium and bulbus arteriosus were cut off and the ventricle was blotted dry and weighed. After one more wash in fresh buffer A it was blotted dry again and cut into smaller pieces (2 × 2 mm), which were incubated for 5 min in 2.5 ml buffer A containing 1 mg subtilisin per g ventricular muscle. At the end of incubation, 12.5 ml buffer A was added and the sample was centrifuged at 15000 g for 5 min. The resulting pellet was re-suspended in 15 ml buffer A and centrifuged at 15000 g for 5 min. The washed pellet was re-suspended in 15 ml buffer A and transferred to a glass homogenizer with a Teflon pestle. The suspension was homogenized at 500 rpm in three rounds of 1-2 seconds and centrifuged for 5 min at 1000 g. The supernatant was retained, while the pellet was re-suspended in 10 ml buffer A, homogenized at 750 rpm in three rounds of 1-2 seconds and centrifuged for 5 min at 1000 g. The two supernatants were spun at 14000 g for 10 min. Each pellet was re-suspended in 0.9 ml buffer A and centrifuged for 5 min at 2000 g. The resulting supernatants were then centrifuged for 15 min at 8000 g, and the pellets containing the mitochondria were resuspended in 0.4 ml buffer A. The isolation of mitochondria was carried out at 0-4°C, and the isolated mitochondria were kept on ice until use within 3 hours.
Recording of ADP-stimulated oxygen consumption
Oxygen consumption of the sample was recorded in an Oroboros oxygraph-2k (Oroboros Instruments, Austria), and the rate of oxygen consumption (nmol O2 ml-1 min-1) was calculated by software developed in our laboratory. To prepare permeabilized fibers for oxygraphy measurements, they were washed twice for 5 min in the R-solution used for oxygraphy. This was either the mammalian R-solution used previously [21–23] and composed for mammalian permeabilized fibers, or the new fish R-solution (see compositions below). These washes served to remove all adenine nucleotides, creatine and phosphocreatine that were present in the S-solution, in which the fibers were kept until use. For isolated cardiomyocytes and isolated mitochondria, which were kept in solutions without these components, a known volume of suspension was added to the oxygraph chamber with fish R-solution. Isolated cardiomyocytes were permeabilized in the oxygraph chamber by the addition of 20 μg ml-1saponin to the chamber at least 4-10 min before the first recordings. This concentration of saponin was chosen on the basis of preliminary experiments, where cells were incubated with 1 mM ADP, and the increase in respiration rate was followed in time until it reached steady state. Among the different saponin-concentrations tested, we observed that 20 μg ml-1 led to a steady state respiration rate within 4-10 min (longer time at cold temperature) that was maintained for more than 30 min (results not shown).
Oxygen consumption was stimulated by stepwise increases in the ADP-concentration. For most experiments, 8 μM cytochrome c and 30 μM atractyloside was added at the end of the ADP-titration to test the intactness of the outer and inner mitochondrial membrane, respectively. At the end of the experiments, permeabilized fibers were taken out of the chamber to determine their dry weight, and allow for the expression of their respiration rate as nmol O2 min-1 mg dw-1. For isolated cardiomyocytes and isolated mitochondria, an aliquot of the suspension was frozen to later determine the protein concentration by a standard bicinchoninic acid (BCA) colorimetric assay (Thermo Scientific). Knowing the volume of suspension added to the oxygraph, respiration rate was calculated as nmol O2 min-1 mg protein-1.
S(skinning)-solution for preparation of permeabilized fibers (originally developed by ) was composed of (mM): CaK2EGTA 2.77, K2EGTA 7.23, MgCl2 6.56, imidazole 20, taurine 20, dithiotreitol 0.5, KOH 50, MES 50, Na2ATP 5.7, phosphocreatine 15, pH adjusted to 7.1 with KOH.
Isolation solution for isolation of cardiomyocytes  was composed of (mM): NaCl 100, KCl 10, KH2PO4 1.2, MgSO4 4, taurine 50, glucose 20, Hepes 10, pH adjusted to 6.9 with NaOH.
Buffer A for isolation of mitochondria  was composed of (mM): sucrose 70, mannitol 220, EDTA 1, Hepes 10, pH adjusted to 7.4 with KOH, 0.5% bovine serum albumin (BSA) added immediately before use.
Mammalian R(respiration)-solution (originally developed by ) was composed of (mM): CaK2EGTA 2.77, K2EGTA 7.23, MgCl2 1.38, imidazole 20, taurine 20, dithiotreitol 0.5, K2HPO4 3, KOH 90, NaOH 10, MES 100, glutamate 5, malate 2, pH adjusted to 7.1 with KOH, 0.2% BSA added immediately before use.
Fish R(respiration)-solution was composed of (mM): KCl 20, K-lactobionate 85, MgCl2 3, KH2PO4 5, EGTA 0.4, dithiotreitol 0.3, glutamate 5, malate 2, taurine 20, Hepes 20, pH adjusted to 7.1 with KOH, 0.2% BSA added immediately before use.
Imaging of isolated cardiomyocytes
Isolated rat cardiomyocytes were provided from other experiments in our laboratory. For transmission images, the cells were mixed in isolation solution and imaged under a Nikon Ti-U microscope with a 60×/NA 1.2 water-immersed objective. For confocal images, rat and trout cardiomyocytes were kept in Ca2+-free Ringer and isolation solution, respectively, containing 30 mM BDM (2,3-butanedione monoxime). The sarcolemma and mitochondria were labeled by incubation for at least 15 min with the membrane potential sensitive dye Di-8-ANEPPS (5 μM; Invitrogen), and the mitochondrial potential sensitive dye Mitotracker Red (1 μM; Invitrogen), respectively. Three-dimensional confocal images (z-stacks) were acquired on a Zeiss LSM 510 confocal microscope with a 63×/NA 1.2 water-immersed objective. The images were deconvolved by software developed in our laboratory using the point spread function recorded at 543 nm .
Data and statistics
Normalized kinetic parameters such as basal respiration rate in the absence of ADP (V0), maximal respiration rate at saturating ADP (Vmax), acceptor control ratio (ACR = Vmax/V0), and the ADP-affinity in terms of the Michaelis-Menten constant (KM ADP) were calculated using in-house software.
All values are presented as mean ± SEM, and statistical tests are described in the legends of the respective figures and tables.
Morphology of rainbow trout compared to rat cardiomyocytes
Development of a new intracellular solution for trout cardiomyocytes
ADP-kinetics of respiration in permeabilized fibres in mammalian R-solution
2.28 ± 0.21
17.95 ± 2.59
7.90 ± 0.91
509 ± 57
2.15 ± 0.25
15.88 ± 2.59
7.38 ± 0.68
252 ± 48
3.39 ± 0.45
22.17 ± 3.46
6.62 ± 0.85
399 ± 34
3.30 ± 0.49
19.37 ± 3.69
5.82 ± 0.77
200 ± 17 *
5.48 ± 0.18
24.22 ± 1.97
4.42 ± 0.32
178 ± 32
5.21 ± 0.45
22.71 ± 3.78
4.26 ± 0.39
129 ± 30
Comparison of intracellular solutions
ADP-kinetics of respiration in permeabilized fibres in fish R-solution
2.34 ± 0.21
24.85 ± 3.44
10.68 ± 1.22
783 ± 160
2.01 ± 0.19
22.6 ± 3.83
11.03 ± 1.62
376 ± 55 *
2.78 ± 0.32
29.13 ± 3.16
10.66 ± 1.01
579 ± 64
2.51 ± 0.08
27.25 ± 2.22
10.96 ± 1.11
301 ± 42 *
3.35 ± 0.07
28.06 ± 3.37
8.40 ± 1.05
293 ± 115
3.37 ± 0.15
30.59 ± 1.83
9.10 ± 0.52
224 ± 42
ADP-kinetics of respiration in permeabilized fibers
ADP-kinetics of respiration in permeabilized cardiomyocytes
ADP-kinetics of respiration in permeabilized cardiomyocytes
4.34 ± 0.37
52.63 ± 6.02
12.09 ± 0.67
93 ± 10
5.40 ± 0.38 **
49.38 ± 4.70
9.11 ± 0.40 **
88 ± 7
5.79 ± 0.74
65.33 ± 5.95
12.64 ± 1.65
77 ± 5
7.45 ± 0.55 *
63.99 ± 4.44
8.88 ± 0.78 *
86 ± 7 *
5.58 ± 1.13
63.21 ± 10.02
12.34 ± 1.08
91 ± 8
6.04 ± 0.86
58.21 ± 9.02
9.56 ± 0.42
89 ± 7
ADP-kinetics of respiration in isolated mitochondria
ADP-kinetics of respiration in isolated mitochondria
11.29 ± 2.34
46.73 ± 12.22
4.05 ± 0.28
6.22 ± 0.99
12.33 ± 4.89
83.18 ± 18.28
7.0 ± 0.64
7.10 ± 0.55
16.75 ± 2.82
131.22 ± 17.29
8.03 ± 0.51
8.65 ± 1.46
The main aim of this study was to verify that rainbow trout cardiomyocytes have intracellular diffusion restrictions by comparing ADP-kinetics of mitochondrial respiration in permeabilized fibers, permeabilized cardiomyocytes and isolated mitochondria. The outcomes were the following: First, isolated trout cardiomyocytes hypercontracted in solutions designed for mammalian preparations, so we had to develop a new "fish R-solution". Second, the discrepancy between fibers and cardiomyocytes suggest that previous results on trout cardiac fibers were affected by incomplete separation of the cells. Third, despite the low density of intracellular membrane structures in trout cardiomyocytes (Fig. 1), diffusion of ADP from solution to the mitochondria in situ is restricted. Fourth, trout cardiomyocytes seem to lack a mitochondrial CK tightly coupled to respiration. The present results on trout cardiomyocytes are very similar to those from other low-performance hearts from for example neonatal rats and rabbits [40, 41].
A new intracellular solution for permeabilized trout cardiomyocytes
It was surprising that isolated cardiomyocytes hypercontracted upon permeabilization in the "mammalian R-solution" that seemed to work for fibers. Therefore, we developed a new "fish R-solution". We were able to compare these solutions on permeabilized fibers. They had a better performance in terms of a lower V0 and higher ACR at high temperatures in the fish R-solution than in the mammalian R-solution (Tables 1 and 3, statistics are given in the Results section). In the fish R-solution, isolated cardiomyocytes maintained their morphology and showed stable steady state respiration rates throughout each experiment (Fig. 2). The addition of cytochrome c at the end of the experiment did not increase respiration rate showing that the outer mitochondrial membrane was kept intact. Atractyloside brought respiration rate down to the basal respiration rate recorded in the absence of ADP showing that the inner mitochondrial membrane was also intact (Fig. 2). Taken together, this validates our use of the fish R-solution for permeabilized trout heart preparations.
Discrepancy between fibers and cardiomyocytes
Kongas et al. suggested that the high apparent KM ADP in fibers may be due to incomplete separation of the cells, which leads to larger diffusion distances . Through the window in the oxygraph chamber, we observed that fibers tend to cluster on top of the magnetic stirrer during oxygraphy measurements. This is avoided with permeabilized cardiomyocytes, where all cells are completely separated, and we observed them to be evenly distributed in the oxygraph solution. Incomplete separation of the cells is not a problem in permeabilized fibers from rat heart, which have the same apparent KM ADP as permeabilized cardiomyocytes [6, 43]. However, studies on trout fibers gave paradoxical results inasmuch as creatine decreased the apparent KM ADP [21, 23], although there seemed to be no mitochondrial CK tightly coupled to respiration .
The present experiments showed that KM ADP in trout fibers is higher than in cardiomyocytes. It depends on temperature and is lowered by creatine, but this is not the case for permeabilized cardiomyocytes. This discrepancy suggests that results from trout fibers were affected by incomplete separation of the cells. It is difficult to separate the cells more in trout heart permeabilized fibers, because the tissue is very soft and fragile compared to rat cardiac tissue. We observed that a more thorough dissection led to mechanically damaged fibers with unstable respiration rates and a low ACR.
It has been questioned whether the high apparent KM ADP in fibers could be caused by unstirred water layers immediately adjacent to the surface of the fibers or cells . From the same line of thought follows whether fibers have a higher KM ADP than cardiomyocytes, because they tend to cluster and thus have thicker unstirred layers than cardiomyocytes. However, two observations from our data strongly suggest that unstirred layers are not the main cause of diffusion restriction. First, the apparent KM ADP should increase with temperature, because metabolic rate (Q10~2 ) would be more limited by diffusion speed (Q10~1.3 ) at higher temperatures. In contrast, we observe a decrease in KM ADP with temperature in fibers (Fig. 3A) and no effect of temperature in cardiomyocytes (Fig. 3B). Second, stimulation of cytosolic CK with creatine would also have an effect in isolated cardiomyocytes. In contrast, creatine only lowers KM ADP in fibers (Fig. 3A) and not in cardiomyocytes (Fig. 3B). Thus, neither the higher KM ADP in cardiomyocytes compared to isolated mitochondria nor the higher KM ADP in fibers compared to cardiomyocytes can be explained by unstirred layers.
One possible explanation for the higher and temperature-dependent KM ADP in fibers could be that perforated sarcolemma is still left to restrict ADP-diffusion between cells. This may become stiffer at colder temperatures and restrict ADP-diffusion more resulting in a higher KM ADP. This would also explain why creatine lowers apparent KM ADP in fibers but not cardiomyocytes. Diffusion across the barriers formed by the sarcolemma in fibers is facilitated by stimulation of cytosolic CK, whereas this is not the case in permabilized cardiomyocytes. This hypothesis could be confirmed by experiments using raster image correlation spectroscopy (RICS) to study diffusion restriction. We recently used this method to determine the diffusion of fluorescent ATP in adult rat cardiomyocytes. Diffusion was anisotropic, being 2 times slower in the longitudinal direction and 3.5 times slower in the transverse direction compared to solution . However, this method only gave information on the overall diffusion coefficients in cells versus solution. It needs further development before it can be used to distinguish diffusion coefficients in different cellular compartments and localize the additional diffusion barriers in fibers compared to cardiomyocytes. Although the exact cause of the discrepancy between fibers and cardiomyocytes is not completely resolved, we conclude that trout cardiac fibers, which have been used in previous studies [21–23], do not give reliable information about intracellular diffusion restrictions in trout cardiomyocytes.
ADP diffusion restrictions and role of creatine kinase in rainbow trout cardiomyocytes
The apparent KM ADP of permeabilized trout cardiomyocytes is independent of temperature and not lowered by creatine. The KM ADP is ~80-90 μM, and this is about ten times higher than of isolated mitochondria (Tables 4 and 5 and Fig. 3). Thus, diffusion of ADP from the medium to the ANT in the inner mitochondrial membrane is restricted. The present study does not give any precise information as to the cause and localization of diffusion restrictions. The magnitude of diffusion restriction in terms of KM ADP is about three times smaller in trout than in rat cardiomyocytes. Thus, t-tubules and SR may still restrict diffusion in rat cardiomyocytes. From the present experiments, we can only conclude that they are not the only cause of diffusion restriction.
Our results suggest that trout heart lacks a mitochondrial CK, because creatine does not lower the apparent KM ADP (Table 4 and Fig. 3). This is in agreement with a previous study . Additionally, the positive charge of mitochondrial CK in rat heart seems to be a prerequisite for binding to the inner mitochondrial membrane , but preliminary experiments with isoelectric focusing suggest that trout heart does not express a positively charged CK isoform (R. Birkedal, unpublished observation). Further experiments will be required to determine whether trout heart expresses a mitochondrial CK. However, the expression of mitochondrial CK does not always correlate with functional coupling to respiration . In tissues such as rat ventricle and oxidative skeletal muscle, where mitochondrial CK (Mi-CK) is tightly coupled to respiration , diffusion restriction by the outer mitochondrial membrane will enhance this coupling . Indeed, mathematical modeling of data from rat heart suggests a moderate restriction of diffusion by the outer mitochondrial membrane and a stronger restriction of diffusion in the cytosol, probably formed by SR together with crowding of cytoplasmic proteins . However, diffusion restriction by the outer mitochondrial membrane seems unfavorable in tissues that lack a tight coupling of mitochondrial CK to respiration. This is the case for adult rat atrium, which expresses Mi-CK [47, 48], neonatal rat and rabbit ventricle, which do not express Mi-CK , and according to the present results also trout ventricle. More experiments and development of a mathematical model for trout cardiomyocytes are needed to quantify diffusion restriction by the outer mitochondrial membrane and cytosolic factors, but the present results argue against diffusion restriction by the outer mitochondrial membrane in trout cardiomyocytes.
Rainbow trout as a model animal to study diffusion restrictions in low-performance hearts
The magnitude of diffusion restriction and the importance of CK in cardiomyocytes seem to relate to metabolism and cardiac mechanical performance. Recent studies have addressed diffusion restriction and metabolic regulation in beating and non-beating HL-1 cardiomyocytes in culture derived from AT-1 mouse atrial tumor cells . Both express cardiac isoforms of connexin, desmin and several ion channels [52, 53], but their morphology is vastly different. The cells are flattened out against the two-dimensional surface on which they are grown. Mitochondria form a reticular network, which seems to have some relation to the sarcomeres found in beating cells [52, 54]. In non-beating cells, sarcomeres are absent . Their metabolic phenotype is glycolytic , and the apparent KM ADP is low (~50 and 25 μM for beating and non-beating cells, respectively) . Indeed, the characteristics of cultured cardiomyocytes are affected by contractile activity and mechanical load , and it seems that for studies of intracellular diffusion restrictions, they cannot yet replace cardiomyocytes that are freshly isolated from working hearts.
Rainbow trout cardiomyocytes seem to have a phenotype that is intermediate between cultured cardiomyocytes and adult mammalian ventricular myocytes. Interestingly, they have these characteristics in common with cardiomyocytes from other low-performance hearts, e.g. neonatal rats and rabbits. Their apparent KM ADP is close to 100 μM and they lack Mi-CK coupled to respiration [40, 41]. Compared to adult mammalian cardiomyocytes, they show greater hypoxia tolerance  and rely more on glycolytic energy production [40, 58], but less so than the cultured cells. In addition, trout and neonatal rabbit cardiomyocytes have similar morphology (compare Fig. 1 with [59, 60]) and possibly also excitation-contraction coupling [61, 62]. Thus, it seems that cardiomyocytes from low-performance hearts are very similar independent of species. It is likely that knowledge about the role of diffusion restrictions and CK in trout cardiomyocytes can be extrapolated to other low-performance hearts.
A new solution was developed for permeabilized trout cardiomyocytes. The results suggest that previous data from permeabilized trout heart fibers were affected by incomplete separation of the cells. This seems to be specific for trout cardiac fibers. The higher apparent KM ADP in fibers could be due to remains of sarcolemma between cells in a fiber bundle. However, even in permeabilized trout cardiomyocytes, which have a very small diameter and low density of intracellular membrane structures, diffusion of ADP from the surrounding medium to the ANT in the inner mitochondrial membrane is restricted. Our results exclude the hypothesis that the main cause of this restriction is unstirred layers. Trout cardiomyocytes do not have a mitochondrial CK coupled to respiration. This argues against diffusion restriction by the outer mitochondrial membrane. Whereas it may be important in rat cardiomyocytes, it is more likely that the diffusion restrictions in trout cardiomyocytes reside in the cytosol. The characteristics of rainbow trout heart are very similar to those of other low-performance hearts such as neonatal rat and rabbit hearts. Most probably, rainbow trout can be used as a model animal to study further the localization and physiological importance of intracellular diffusion restrictions in low-performance hearts in general.
List of abbreviations
acceptor control ratio (= Vmax/V0)
adenine nucleotide translocase
bovine serum albumin
intracellular energetic unit
- KM ADP:
mitochondrial Michaelis Menten constant for ADP
mitochondrial chloride intracellular channel
sarco-endoplasmic reticulum Ca2+-ATPase
basal respiration rate before addition of ADP
maximal respiration rate.
We wish to thank Mervi Sepp for writing the software for analysis of oxygraphy data, and Martin Laasmaa for writing the software to deconvolve confocal images.
The research was supported by Welcome Trust Fellowship no. WT081755 MA and the Estonian Science Foundation grant no. ETF8041 (Ph.D. stipend for N. S.).
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