Calcium homeostasis in red blood cells of dialysis patients in dependence of erythropoietin treatment

Abstract

Previous studies provided evidence for a massively increased intracellular Ca2+ concentration in red blood cells (RBCs) of patients with end-stage renal disease (ESRD) (Paschen et al., 1971; Gafter et al., 1989), whereas the dialysis procedure itself led in average to an even slightly decreased RBC's Ca2+ content (Paschen et al., 1971; Dlugaszek et al., 2008). Based on a single cell approach we could qualitatively confirm these results (Figure ​(Figure1A,1A, 2 leftmost columns), although the extend of the Ca2+ increase was smaller compared to the cited investigations, which is presumably caused by differences in the methodology. Figure 1 Ca2+ in RBCs of healthy donors and end-stage renal disease (ESRD) patients with a renal anaemia. If patients were under EPO treatment, the last EPO administration was within 5 days of blood sampling. All experimental procedures are previously described ... There is a good knowledge of Ca2+ related processes in RBCs (Bogdanova et al., 2013). Additionally, an increased intracellular free Ca2+ concentration in RBCs has been proposed as a trigger for intracellular aggregation (Andrews and Low, 1999; Kaestner and Bernhardt, 2002) as well as for endothelium-RBC adhesion (Hebbel et al., 1980; Mohandas and Evans, 1985) and experimental evidence has been provided (Noh et al., 2010; Steffen et al., 2011; Borst et al., 2012; Kaestner et al., 2012). The molecular identity of Ca2+- and non-selective cation channels in the RBC membrane is steadily increasing (Kaestner, 2011) and comprise of, e.g., the CaV2.1 (Andrews et al., 2002), the TRPC6 (Foller et al., 2008), the NMDA-receptor (Makhro et al., 2013), and the Piezo1 (Zarychanski et al., 2012). The effect of erythropoietin (EPO) on RBCs ion homeostasis is controversially discussed. The group of Florian Lang found an inhibition of non-selective cation channels by EPO with a decreased number of eryptotic RBCs if patients were treated with EPO (Myssina et al., 2003). However, once Ca2+ entered the RBC, EPO has no beneficial effect toward the eryptotic symptoms caused by Ca2+ (Vota et al., 2013). In contrast to RBCs, hematopoietic progenitor cells display an increased cation-channel activity upon EPO exposure (Cheung et al., 1997; Tong et al., 2008). Because of its hematopoiesis stimulating properties, EPO became a widely used medication for treatment of anemic patients, including chronic renal disease, hematologic disorders, and acquired immune deficiency syndrome (Palmer et al., 2010; Goodnough and Shander, 2013). However, several studies highlighted the problem of an increased risk of thrombus formation, especially venous thromboembolism, in patients undergoing EPO therapy (Singbartl, 1994; Kliger et al., 2012; Goodnough and Shander, 2013). Therefore we investigated the free Ca2+ concentration in RBCs from ESRD (dialysis) patients under EPO treatment. Blood samples from healthy donors, ESRD patients and EPO treated ESRD patients were analyzed by fluorescence live cell imaging as previously described (Wang et al., 2013) (Figure ​(Figure1).1). As depicted in Figure ​Figure1A,1A, at rest, RBCs from ESRD patients show higher Ca2+ concentration compared with healthy donors, while EPO treatment let to a slightly decreased free internal Ca2+ concentration, indicating an inhibition of constitutively active channels in resting RBCs. Although the histograms (Figure 1Ab) give an impression of the distribution, the method lacks quantitative information concerning the Ca2+ concentration (Kaestner et al., 2006). However, when compared to control conditions, the width of the distribution of Ca2+ content is wider in ESRD patients or EPO-treated ESRD patients, leading to the conclusion that the cellular heterogeneity is greater in patients than in healthy subjects. In a further step we investigated the Ca2+ influx in RBC from healthy donors and ESRD patients after hormonal stimulation in dependence of EPO treatment (Figure ​(Figure1B).1B). As a stimulation substance we selected prostaglandin E2 (PGE2), which is released from activated platelets (Smith et al., 1973) but can also be released from RBCs themselves when they pass small capillaries (Oonishi et al., 1998). The curves in Figure 1Ba present typical example traces for Ca2+ curves in RBCs, while Figure 1Bb shows the statistical analysis. Healthy patients show an increase in Ca2+ after PGE2 stimulation as we have previously shown (Kaestner et al., 2004). EPO treatment prevents Ca2+ entry resulting in Ca2+ levels below control conditions confirming the results of the Lang group (Myssina et al., 2003). However, pretreatment with EPO even suppressed the Ca2+ entry provoked by PGE2. In ESRD patients, PGE2 stimulation leads to a Ca2+ increase, which is significantly higher than in RBCs of healthy donors. In EPO treated ESRD patients the PGE2 induced Ca2+ increase was significantly suppressed compared to RBCs of non-treated patients even in the putative absence of EPO during the experiment. The results of Figure ​Figure11 suggest that the clinically observed thrombotic complications in patients treated with EPO seem not to be primarily caused by an elevated Ca2+ content of RBCs of these patients. However, it is hypothesized that EPO causes thrombosis as a result of inflammation (Tobu et al., 2004). The elevated basal Ca2+ level in RBCs of ESRD patients (Paschen et al., 1971; Gafter et al., 1989; Figure ​Figure1A)1A) may enhance a blood clotting once initiated by an inflammation processes. It is a substantial finding that the response of RBC to hormonal stimulation or other treatments, like the dialysis itself, in terms of Ca2+ entry shows a wide variation between RBC within a population, but also between different individuals (Paschen et al., 1971; Wang et al., 2013; Figure 1Ba). In light of the above statements concerning the thrombotic events and the molecular players, the perspective of medical treatment must be based on a personalized diagnosis followed by a personalized medication. This applies to ESRD patients as well as for treatments of other anemias. Techniques and procedures allowing such an individualized approach presumably based on the combination of RBC population measurements and single cell techniques (Minetti et al., 2013) need urgently to be developed.