Electrolyte Composition of Mink (Mustela vison) Erythrocytes and Active Cation Transporters of the Cell Membrane
© The Author(s) 2001
Received: 04 April 2000
Accepted: 23 January 2001
Published: 30 June 2001
Red blood cells from mink (Mustela vison) were characterized with respect to their electrolyte content and their cell membranes with respect to enzymatic activity for cation transport. The intra- and extracellular concentrations of Na+, K+, Cl-, Ca2+ and Mg2+ were determined in erythrocytes and plasma, respectively. Plasma and red cell water content was determined, and molal electrolyte concentrations were calculated. Red cells from male adult mink appeared to be of the low-K+, high-Na+ type as seen in other carnivorous species. The intracellular K+ concentration is slightly higher than the extracellular one and the plasma-to-cell chemical gradient for Na+ is weak, though even the molal concentrations may differ significantly. Consistent with the high intracellular Na+ and low K+ concentrations, a very low or no ouabain-sensitive Na+,K+-ATPase activity and no K+-activated pNPPase activity were found in the plasma membrane fraction from red cells. The Cl- and Mg2+ concentrations expressed per liter cell water were significantly higher in red cells than in plasma whereas the opposite was the case with Ca2+. The distribution of Cl- thus does not seem compatible with an inside-negative membrane potential in mink erythrocytes. In spite of a steep calcium gradient across the red cell membrane, neither a calmodulin-activated Ca2+-ATPase activity nor an ATP-activated Ca2+-pNPPase activity were detectable in the plasma membrane fraction. The origin of a supposed primary Ca2+ gradient for sustaining of osmotic balance thus seems uncertain.
Keywordserythrocytes plasma electrolytes red cell mink red cells Na+,K+-ATPase membrane potential osmotic balance PM-CaATPase
The plasma membrane-embedded (Na++K+)-activated ATPase (Na,K-ATPase, EC 126.96.36.199) of mammalian cells is usually supposed to have an essential role in counterbalancing passive ionic leaks and oncotic forces from intracellular proteins and fixed phosphate groups, i.e. in cell volume regulation [6, 14]. There are, however, a few exceptions from this general principle, in which case a plasma membrane-bound Ca2+-ATPase and a Na+/Ca2+-exchange mechanism are usually supposed to have similar roles [18, 19, 21].
It has been known for years that red blood cells in some mammalian species may be devoid of Na,K-ATPase and yet be able to maintain ionic balance and cell volume. Some carnivorous species, e.g. the cat and the dog, have low-potassium erythrocytes due to a lack of plasma membrane Na,K-ATPase [2, 4] and Na+/Ca2+ exchange may partly account for cell volume maintenance [18, 19, 21]. Also red cells from ferrets (Mustela putorius furo), i.e. a Mustelidae species belonging to a collateral branch of the carnivorous phylogenetic tree have high sodium and low potassium content [9, 16]. In other species, e.g. sheep and goat, the eythrocytes may be of a high-potassium or a low-potassium type . In the latter case the number of sodium pumps per red cell may be reduced or, more likely, the Na,K-ATPase activity is inhibited by a membrane-bound inhibitory factor closely related to the blood group L antigen . The K+ concentration is relatively low but not that low as seen in carnivorous species.
To our knowledge, red cells from the only carnivorous species used for large-scale animal production, the domestic mink (Mustela vison), were never characterized with respect to electrolyte composition. In this study the ionic type of red blood cells of the domestic mink is characterized, and moreover, the plasma membrane of mink red cells with respect to the main ion-transporting ATPases: The (Na++K+)-activated ATPase and the Ca2+-activated ATPase (PM-Ca2+ ATPase).
Materials and methods
Preparation of plasma, red cell contents and erythrocyte plasma membranes
Domestic mink (Mustela vison) from a fur research farm free of plasmacytosis were used in this study. Twelve adult male mink selected for pelting at the end of the mating season in 1998 were anaesthetized by means of an intraperitonal injection of pentobarbital (25 mg/kg). Another 12 adult male mink (1999a) and 12 adolescent (7 months) male mink were sacrificed for follow-up studies (1999b). About 10 ml of blood was obtained by heart puncture from each animal. The blood was stabilized by collection in heparinized tubes, handled and transported at 0–2°C for about 2 h and then rewarmed and kept at room temperature before separation. Plasma was obtained after separation for 5 min at 1600 g (Heraeus Microfuge 1.0). The intermediary layer (buffy coat) was carefully withdrawn and discarded. After resuspension to the original volume in 0.9% NaCl the erythrocyte fraction was washed 3 times by sedimentation at 1600 g for 5 min. Finally the erythrocyte fraction was suspended in 300 mM sucrose (final volume 25 ml) and washed by sedimentation at 20,000 g (Beckman, rotor 50.2 Ti). The supernatant was carefully withdrawn and discarded. 250 μl of the packed erythrocytes were withdrawn for determination of dry matter. The remaining volume of packed erythrocytes was weighed (about 3 g), suspended in exactly 6 ml of a medium containing 20 mM imidazole + 0.5 mM EDTA (pH 7.4, adjusted with HNO3) for hemolysis and centrifuged for 15 min at 35,000 g (Beckman, rotor 70.1 Ti). Supernatant was withdrawn for determination of Na+, K+, Cl-, Ca2+ and Mg2+. The sediment was resuspended in 25 ml of the imidazole/EDTA buffer and washed twice by precipitation at 35,000 g for 15 min, then twice in 20 mM imidazole and finally once in 40 mM imidazole + 40 mM histidine (pH 7.1). The individual sediments were pooled, resuspended in the same buffer and homogenized in a tightly fitting Teflon glass homogenizer surrounded by an ice bath. The final product, the cell membrane fraction, was stored at -20°C until determination of enzymatic activity.
In one series (1999b) a possible release or uptake of electrolytes during washing was determined in the following way: All supernatants from washings were recovered, weighed and used for determination of Na+, K+, Cl- and Mg2+. At each step during washing the weight of the precipitate including residual plasma, saline or sucrose was determined. The difference between this weight and the original weight of packed erythrocytes was taken as contaminating plasma, saline or sucrose. In this way, step-by-step transfer of electrolytes between erythrocytes and plasma could be calculated and accounts of step-by-step and net efflux or influx of electrolytes made. Due to contamination by Ca2+ of redistilled water and reagents, a similar assessment of Ca2+ release or uptake by erythrocytes during washing was not undertaken.
Measurements on plasma, saline and sucrose used for washing, and on erythrocyte contents (lysate)
Dry matter of plasma and erythrocyte fraction was determined by heating at 80°C until constant weight. Molar concentrations of Na+ and K+ were determined using a Radiometer (Copenhagen, Denmark) FLM3 flame photometer with lithium as internal standard. Ca2+ and Mg2+ were determined by atomic absorption spectrophotometry (Philips PU 9200; Pye Unicam, Cambridge, UK). Aliquots of plasma and erythrocyte content were adequately diluted and compared with standards of CaCl2 (6.25–50 μM) with addition of 0.2% (w/v) KCl or with standards of MgCl2 (10–400 μM). Determination of chloride was carried out with an ABU91 Autoburette from Radiometer in which 1 mM AgNO3 was titrated with 1 mM NaCl for calibration. (Data on intracellular Cl- in 1998 are missing due to adjustment of the imidazole/EDTA buffer used for cell lysis with HCl). In control experiments it was shown that addition of bovine hemoglobin (Sigma) corresponding to an estimated concentration in lysate from mink erythrocytes (0.1 g/ml) did not influence chloride determination and neither did albumin in plasma. Calculation of molal concentrations of Na+, K+, Ca2+, Mg2+ and Cl- was carried out by dividing the molar concentrations with (1-fd) where fd is the fraction of dry matter.
Enzymatic activities of erythrocyte plasma membrane fraction
ATPase activities were determined at 37°C by the coupled assay utilizing the NADH/NAD+ conversion in the presence of auxiliary enzymes . Na+,K+-ATPase determined in the absence and the presence of 10-3 M ouabain was supposed to represent total and basal (~unspecific Mg2+-ATPase) hydrolytic activity, respectively. The K+-activated hydrolysis of the artificial substrate pNPP (K+-pNPPase) was assayed as described elsewhere . The activity obtained by substitution of K+ with Na+ was taken to represent unspecific activity. Total and basal hydrolytic activity related to Ca2+-ATPase were determined at 0.1 mM Ca2+ and 1 mM EDTA, respectively. Calmodulin (phosphodiesterase 3':5'-cyclic nucleotide activator from Sigma) at 80 nM was preincubated with the membrane fraction for 5 min before addition of Ca2+ and substrate . Ca2+-pNPPase activity was determined in the presence and absence of 0.5 mM ATP.
Dry matter and electrolyte concentrations in plasma and erythrocytes before (first column: mmoles per l plasma or per kg erythrocytes) and after correction for dry matter (second column: mmoles per kg H2O). Values are ± SEM
(n = 12)
7.81 ± 0.16
151.5 ± 1.3
164.3 ± 1.4
3.9 ± 0.3
4.4 ± 0.3#
102.5 ± 1.3
111.1 ± 1.3
(n = 12)
8.56 ± 0.12
152.3 ± 0.5
166.7 ± 0.5**
4.2 ± 0.0
4.6 ± 0.0**
99.7 ± 1.5
109.0 ± 1.7**
(n = 12)
7.88 ± 0.10
152.1 ± 0.4
165.2 ± 0.4**
3.8 ± 0.1
4.1 ± 0.1*
112.5 ± 1.0
121.9 ± 1.0**
(n = 11)
38.75 ± 0.72
98.2 ± 4.9
160.7 ± 8.3
2.2 ± 0.3
3.5 ± 0.4#
(n = 12)
41.49 ± 0.21
83.2 ± 1.8
142.3 ± 3.0**
1.1 ± 0.1
1.9 ± 0.1**
98.6 ± 2.9
168.6 ± 5.1**
(n = 12)
42.51 ± 0.30
75.6 ± 2.1
131.4 ± 4.2**
2.0 ± 0.1
3.5 ± 0.1*
82.8 ± 2.6
144.1 ± 4.7**
(n = 12)
1.89 ± 0.03
2.05 ± 0.04**
0.88 ± 0.05
0.95 ± 0.06**
(n = 12)
2.11 ± 0.04
2.31 ± 0.04**
1.33 ± 0.02
1.45 ± 0.02**
(n = 12)
2.47 ± 0.02
2.68 ± 0.02**
1.11 ± 0.02
1.21 ± 0.02**
(n = 11)
0.086 ± 0.006
0.138 ± 0.010**
2.98 ± 0.15
4.92 ± 0.30**
(n = 12)
0.052 ± 0.006
0.088 ± 0.010**
3.89 ± 0.20
6.64 ± 0.35**
(n = 12)
0.098 ± 0.004
0.171 ± 0.006**
4.01 ± 0.25
6.97 ± 0.43**
It is seen that the intracellular concentration of K+ is very low and apparently lower than the concentration in plasma (see below), whereas the intracellular concentration of Na+ is nearly as high as the extracellular one. A significant difference in Na+ concentrations intra- and extracellularly may, however, exist, at least according to data obtained in 1999. The intracellular molal concentrations of Cl- and Mg2+ are significantly higher than the respective extracellular concentrations. For Ca2+ an opposite directed concentration gradient exists.
Accumulated values of electrolytes from 4 × washing and in the final lysate from erythrocytes (1999b). An estimated value for the sum in molal concentration is given in the last column. Number of observations in brackets.
4 × washing
mmoles per kg red cells ± SEM
9.76 ± 3.01 (11)
75.58 ± 2.12 (12)
85.34 ± 3.68
4.11 ± 0.10 (11)
2.00 ± 0.08 (12)
6.11 ± 0.13
2.20 ± 3.27 (12)
82.78 ± 2.55 (12)
84.98 ± 4.15
0.25 ± 0.02 (10)
4.01 ± 0.25 (12)
4.26 ± 0.25
Hydrolytic activities of mink erythrocyte membrane fraction, (Na++K+)-activated ATPase activity in the absence and the presence of ouabain, pNPPase activity in the presence of K+ or Na+, Ca+-activated ATPase activity in the presence of Ca+ or EDTA ± calmodulin and pNPPase activity in the presence of Ca+ ± ATP. Number of determinations in brackets.
nmol·(mg protein)-1·min-1 ± SEM
18.4 ± 0.9 (9)
15.6 ± 2.3* (7)
(Na++K+)-ATPase + ouabain
14.5 ± 2.1 (7)
9.6 ± 1.4* (7)
12.7 ± 0.8 (4)
11.3 ± 1.4 (3)
11.6 ± 2.1 (3)
10.2 ± 0.2 (3)
Activity in the presence of Ca2+
22.5 ± 1.2 (7)
Activity in the presence of Ca2++calmodulin
19.8 ± 1.8 (7)
37.8 ± 12.8 (4)
Activity in the presence of EDTA
17.3 ± 1.6 (5)
Activity in the presence of EDTA+calmodulin
24.6 ± 1.9 (5)
23.4 ± 4.7 (4)
Ca2+-pNPPase (- ATP)
7.4 ± 0.1 (3)
Ca2+-pNPPase (+ ATP)
6.4 ± 0.1 (3)
Similarly, calcium pump related hydrolytic activities of the erythrocyte membrane fraction were measured as the calmodulin-activated Ca2+-ATPase and as the ATP-activated Ca2+-pNPPase activity. As also seen from Table 3 no significant increase in the two activities was seen with calmodulin or ATP. It seems therefore that mink red cells, as well as being totally deprived of Na,K-ATPase, are also deficient in calcium pump activity.
The aim of the present study is a characterization of electrolytes in plasma and red cells from the only carnivorous species used for large-scale animal production, the domestic mink (Mustela vison). The erythrocyte membrane is moreover characterized with respect to (Na++K+)- and Ca2+-activated ATPase activity. The perspectives associated with the transmembranous concentration gradients, expressed per liter plasma water and cell water, for Na+, K+ and, in particular, for Cl- are also focused upon in this study. On the other hand, a more comprehensive analysis of the mink erythrocyte membrane with respect to channels and carriers for electrolyte transport is outside the scope of the present study.
It appears that erythrocytes from healthy, domestic male mink, whether adult or adolescent, are of the low-K+, high-Na+ type as seen in other carnivorous species and that the plasma membrane of red cells is practically devoid of ouabain-sensitive Na,K-ATPase activity. The generally accepted principle, that body cells as well as red blood cells of most mammalian species have high intracellular K+ and low Na+ concentrations, may have other exceptions, however.  recently described a fraction (some 4%) of sicle cells from human beings with sicle cell anemia and an extremely low proportion of normal red cells that appeared to be of the low-K+, high-Na+ type.
One practical aspect of the odd electrolyte distribution between mink red cells and plasma is the following: A minor degree of hemolysis will not significantly change plasma-K+, which is a parameter of clinical significance in some mink diseases . Another aspect is an underscore of the high plasma osmolality of mink plasma [24, 5], in the present study indicated by the high plasma Na+ concentration, which may give rise to further investigations. Since mink blood is easily available in some countries, e.g. Canada and Denmark, during the pelting season, the red cells of this species seem ideal for further studies on osmoregulation in the absence of an active sodium pump.
The plasma concentrations of electrolytes in the 1998 study are almost the same as found in the 2 series of experiments in 1999, whereas the intracellular concentrations may differ somewhat though the same procedure was used each time. The plasma concentrations of Na+, K+, and Mg2+ in all mink of the present study and of Cl- and Ca2+ in adolescent mink (Table 1, experiment 1999b) are also almost exactly identical to those previously found in healthy mink dams [24, 5], whereas Cl- and Ca2+ are somewhat lower in adult male mink (Table 1, experiments 1998 and 1999a). The high plasma-Na+ concentration is consistent with a very high plasma osmolality, of the order of 310–330 mOsm, in mink as seen in previous studies [24, 5]. The tonicity of 300 mM sucrose used for the final wash of mink red cells thus does not exceed that of erythrocytes and hypertonic cell shrinkage seems unlikely.
No correction was made for trapped sucrose in the final wash of the mink red cells with 300 mM sucrose, which may have added no more than 0.2% dry matter (0.3 M × 342 (MW) × 0.02) provided that closely packed red cells contain a maximum of 2% trapped water space . A lower concentration of dry matter was found in ferret red cells but observations of considerably higher values were quoted from the literature . Irrespective of a trivial correction of dry matter content for trapped sucrose (about 0.2% compared to 40% dry matter, i.e 0.5 relative per cent) and thus in calculation of red cell water content, the intracellular concentrations are dramatically increased when expressed per liter cell water.
As to the intracellular concentrations of electrolytes, similar concentrations of Na+ and Mg2+ as the present ones were found in red cells from ferret by  when expressed per liter original cells, although they used very different media during separation. This does not hold for the Ca2+ concentration that was 5–10 times lower and the K+ concentration that was 2–3 times lower than found in the present study, the latter parameter after correction for K+ efflux during washing of the red cells. Our washing procedure using isotonic NaCl and sucrose was anticipated not to be too harmful to mink erythrocyte permeability as noticed in a study with dog red cells  in which the water content was shown to be dependent on impermeant sucrose and Na+ of the media. In one series of the present experiments (Table 1, 1999b) a possible leak of electrolytes was determined (Table 2). Since the intracellular concentrations for Na+ and Cl- were lower in this series than otherwise found (Table 1) a maximum leak might have taken place in this experiment. No dramatic net efflux of Mg2+ (5.9%), Cl- (2.6%) or Na+ (11.4%) was found however, whereas the intracellular K+ concentration was reduced to 1/3. Even when the intracellular K+ concentration is tripled the main conclusion, that mink erythrocytes are of the high-Na+, low-K+ type, is still valid, however.
When expressing concentrations per liter cell water a weak, though significant, chemical gradient for Na+ seems to exist across the red cell membrane even after correction for efflux during washing. At a very low, inside positive, membrane potential Na+ may be near equilibrium (see below). In contrast, after correction for efflux of K+ during the washing procedure the intracellular concentration of this cation seems somewhat higher than the extracellular one. On the other hand, the intracellular concentration of K+ in mink red cells is still far below that seen in most mammalian species.
There are few studies on the intracellular concentration of Cl- in red cells from low-K+ species. Using a buffered physiological medium containing 150 mM Cl- for suspension of ferret red cells and 36Cl as tracer  found a ratio of 1.50 for external to internal chloride concentration, i.e. a somewhat lower intracellular chloride concentration than in the present study after separation of erythrocytes from 110–120 mM Cl- in plasma. Similarly,  made an estimate of the intracellular chloride concentration in dog red blood cells by using a media containing 36Cl and 15 min of equilibration. Somewhat lower intracellular Cl- concentrations per liter cell water were obtained by this method than in the present study at comparable external salt concentrations. Even in the absence of any corrections for dry matter the intracellular concentration of Cl- in mink erythrocytes is nearly as high as the extracellular one. Expressed per liter cell water the intracellular Cl- concentration is significantly higher than that in plasma water. After correction for membrane leak during washing of the red cells the Cl- concentration in mink red cells is nearly as high as the concentration of monovalent cations. For electroneutrality, however, a number of small intracellular electrolytes has to be taken into account in addition to the net charge of hemoglobin. In the above mentioned study on dog red cells  a net negative charge of these intracellular electrolytes and a small net negative charge of hemoglobin was calculated for counterbalancing a net positive charge from monovalent cations. A net negative membrane potential set by chloride as seen in red cells from other species  seems incompatible with the high intracellular concentration of this anion or the membrane potential would even have an opposite direction (inside positive). Chloride and sodium concentrations in mink plasma and erythrocytes would suggest a membrane potential of 7–8 and 3 mV, respectively. Using an indirect method that would imply hydrogen ion equilibrium according to the membrane potential after addition of a protonophore,  calculated a membrane potential of -10 mV in ferret red cells.
Ca2+ is definitely not equally distributed in mink plasma and in red cells. Another divalent cation, Mg2+, has the opposite distribution. A mechanism for extrusion of red cell Ca2+ must exist. Provided Na+ were significantly out of equilibrium a Na+/Ca2+-exchange mechanism might have been (part of) the explanation. Uphill Ca2+ transport cannot be fuelled by passive Na+ entry, however, in the absence of a membrane-bound Na,K-ATPase and thus a primary electrochemical gradient for this ion . A very low and for one membrane preparation no significant ouabain-sensitive (Na++K+)-activated ATPase activity and no K+-activated pNPPase activity were seen in the present study. Irrespective of the ionic conditions employed, more or less the same hydrolytic activity of the cell membrane fraction was measured. This activity is thus probably due to some unspecific Mg2+-ATPase/phosphatase associated with the erythrocyte membrane fraction. Almost the same basal Mg2+-ATPase activity was measured in human red cells, whereas the calmodulin-activated ATPase activity was 2–3 times higher [11, 13]. Likewise, a ouabain-sensitive (Na++K+)-activated ATPase activity of 45 ± 3 nmol.(mg protein)-1.min-1 was measured in high-potassium (HK) red cells from a rare variant of a Japanese dog whereas the activity in LK cells was nil .
From our present knowledge and in the absence of a Na,K-ATPase and a Na+ gradient the low intracellular concentration of Ca2+ has to be due to a primary Ca2+ pump. A Na+/Ca2+-exchange mechanism as found in ferret red cells  may then have an opposite role: extrusion of Na+ for counterbalancing the oncotic forces created by internal hemoglobin. Surprisingly, we were unable to measure any Ca2+-activated ATPase activity, irrespective of the presence of calmodulin or not, indicating no or a very low concentration of plasma membrane Ca2+-ATPase (PM-CaATPase). Similar conclusions were reached by  and by  in dog red cells though the latter authors presented indirect evidence of a calmodulin-activated Ca2+-ATPase. When dog red cells were exposed to the ionophore A23187 in the presence of Ca2+ a faster loss of ATP was seen . Similarly,  showed that resealed ghosts of dog red cells were able to extrude Ca2+, provided ATP was incorporated into them. At a low (inside negative) membrane potential and at a supposed exchange ratio of 3:1 a Na+/Ca2+-exchange mechanism might be effecient for extrusion of Na+ driven by a Ca2+ gradient created by an active extrusion of Ca2+ [18, 19, 21].
In conclusion: Mink red cells appeared to be of the low-K+ type consistent with a very low or no ouabain-inhibitable Na+,K+-ATPase activity and no K+-activated pNPPase activity. When expressed per liter water a weak plasma-to-cell concentration gradient for Na+ and a weak opposite-directed K+ gradient seem to exist An unexpected high intracellular Cl- concentration was found. Osmotic balance may be sustained by a primary Ca2+ gradient the origin of which seems uncertain.
Thanks are due to Ms. Tove Lindahl Andersen, Ms. Edith Bjørn Møller and Mr. Toke Nørby for excellent technical assistance. This study was supported by the Danish Biomembrane Research Centre.
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