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Abstract

In general, reactive nitrogen species, like nitric oxide (NO) and peroxynitrite are classified in primary and secondary according its benefic or deleterious effects respectively. Multiple benefic roles through the body has been attributed to nitric oxide (NO), a key signaling molecule, which acts as vasodilator relaxing smooth muscles of arteries; participates in the blood pressure control; hinders the initiation of inflammation NO liberated from endothelium cells or lymphocytes to intravascular corporal fluid enter into erythrocytes through membrane band 3 protein being after captured by deoxyhemoglobin or by oxyhemoglobin. Inside the erythrocytes several chemical reactions occur with generation of S-nitrosoglutathione a NO reservoir molecules and NO derivatives (NOx) molecules namely nitrite, nitrate and peroxynitrite. The erythrocyte acts as sensor of the tissues oxygen partial pressure and consequently change its oxygen levels lead along with NO contents. NO is released through band 3 protein into the blood, at microcirculatory network, in tissues with low oxygen partial pressure. The aim of this mini review was to present the erythrocyte signal transduction pathways associated with NO and S-nitrosoglutathione efflux, metabolic behavior of the NO reservoir molecules and NO reactive species in human erythrocytes under several biological conditions. For examples, the effects of external amphipathic molecules, fibrinogen, and internal manipulation of protein phosphorylation degree and redox status on erythrocyte. NOx, NO and S-nitrosoglutathione efflux levels are herein included. Erythrocyte NO efflux evidenced as biomarkers of inflammatory vascular diseases will be herein highlighted.

Keywords

erythrocyte, nitric oxide, peroxynitrite, nitrite, nitrate, s-nitrosoglutathione; phosphoinositide-3 kinase, adenylyl cyclase

Mini review

Nitric oxide (NO) produced by endothelial cells and T-lymphocytes, once released into the blood circulation, can enter the erythrocyte membrane through band 3 protein [1]. Erythrocytes assure the transport of oxygen and nitric oxide obtained from the lungs under high values of oxygen partial pressure (PaO₂) to systemic tissues, with lower PaO₂, where partially liberated are [2]. The primary erythrocyte function concerning the oxygenation tissue is accompanied by the mobilization of NO [3]. Thus, once NO reaches the intra-globular compartment binds to oxyhemoglobin forming the S-nitrosohemoglobin (SNO-Hb) molecules and several reactions happen, such as NO reacting with the superoxide anion forming peroxynitrite (ONOO−), which subsequently yields nitrite and nitrate [4]; all together these molecules receive the nomination of NO derivatives (NOx). Nitrate production in erythrocytes occurs in the presence of oxygen and oxyhemoglobin and can be converted to nitrite by the action of methemoglobin reductase [4]. It is also known that erythrocytes may release nitric oxide in the microcirculation under low oxygen tension [2]. The efflux of NO from erythrocyte occurs through a trans-nitrosylation process involving the thiol group of the band 3 protein that receives NO from SNO-Hb [4], however the precise transport mechanism is not yet clarified. The GSNO efflux from erythrocytes or red blood cells (RBCs) has also been observed by us [5]. Using fluorescence microscopy, we observed NO inside human erythrocytes after acetylcholine (ACh) stimulation and we were the first to quantify the NO efflux from erythrocytes with a potentiometer device [4,6].

But until now, the majority of the published studies in the literature quantified plasma or erythrocyte nitrite but calling it NO. When NO was recognized as a vasodilator [7], we question if RBCs deformability will be affected by the presence of NO. So, using SpermineNONOate (a NO donor) and ACh as stimulator of NO efflux from erythrocytes, we observed an increase in RBCs deformability [8]. Opposite effects on the oxygen affinity to hemoglobin, experimentally quantified as P50, was obtained with ACh and SpermineNONOate with which we observed, respectively augmented and impairment P50 values, meaning a decrease and an increase in oxygen affinity for hemoglobin [8]. The NO donor behavior has an allosteric factor of oxygen affinity for hemoglobin, which was later confirmed [9]. Our experimental results with erythrocytes showed NO and oxygen efflux in the presence of ACh in opposition to NO influx and oxygen binding to Hb in the presence of a NO donor [8]. These results are identical to the ones described above about the RBCs gas transportation in tissues with high and low PaO₂ [2]. As far as is known, NO enters into erythrocytes and turn out through membrane band 3 protein [10]. Erythrocyte membrane band 3 protein contains tyrosine residues able to become phosphorylated, by protein tyrosine kinases (PTK: p72syk or p53/56lyn), which could be dephosphorylated by protein tyrosine phosphatase (PTP). A dynamic balance between band 3 phosphorylation and dephosphorylation occurs in normal erythrocytes [11]. Both PTK and PTP enzyme activity are dependent on the protein kinase C (PKC) activity which phosphorylates both enzymes becoming PTP inactive and PTK in an active state [11]. So, our studies pursuit to search answers about the signal transduction mechanism associated with erythrocyte NO mobilization under influence of amphipathic and hydrophilic molecules, protein phosphorylation degree and redox status of erythrocytes.

Nitrogen oxidative species levels and internal proteins of the human erythrocytes in health and inflammatory vascular diseases

Acetylcholine (ACh) is a ubiquitous molecule produced by endothelial cells and T lymphocytes and the mechanism of ACh resultant from endothelial cells into blood circulation was recently confirmed [4,12]. In erythrocyte membrane we demonstrate a cross talk between band 3 protein and acetylcholinesterase (AChE) enzyme binding to its natural substrate, ACh or to an inhibitor, velnacrine maleate (VM) [13]. It was also confirmed that the active AChE- ACh and inactive AChE–VM complexes conformations associated with adenylyl cyclase through G_iαβ protein result in lower adenylyl cyclase (cAMP) production [13]. It was also shown that both enzyme complex conformations activate protein kinase C (PKC) which in turn inhibits, by phosphorylation, the phosphodiesterase -3 (PDE-3), without changes on cAMP concentration [14].

When AChE-ACh enzyme complex occurs in RBCs membrane, high levels of NO efflux, nitrite and nitrate concentrations were observed in the absence or presence of band 3 phosphorylation induced by calpeptin, the inhibitor of PTP [4,14]. Although, the GSNO levels are independent of band 3 phosphorylation degree [14].

Higher significant levels of NO efflux from RBCs were achieved when band 3 is dephosphorylated by the p72syk inhibitor in the presence of the inactive enzyme complex AChE-VM, when compared to the AChE-ACh complex [14].

Regarding the nitrite and nitrate levels they are independent of band 3 phosphorylation degree when the AChE-VM inactive complex is present in the RBCs membrane [14].

Both PTK and PTP enzymes are also phosphorylated by protein kinase C (PKC) resulting in PTP inactivation and PTK activation [11]. When RBCs present a higher band 3 protein phosphorylation status, this is followed by an increased AChE enzyme activity [13].

When the band 3 protein phosphorylation results from the presence of a PKC activator, high values of NO efflux are obtained with AChE-ACh, at variance of lower values verified under PKC inhibition [5,15]. These results reinforce the association between band 3 phosphorylation and NO efflux from erythrocytes and confirm the role of cAMP levels in the signal transduction pathway; its involvement is dependent of PKC activators or inhibitor concentration by direct manipulation in erythrocytes.

The NO efflux from erythrocytes measured in the presence of AChE-VM was lower in relation to those determined in the presence of AChE-ACh [14]. In erythrocytes the inactive AChE-VM enzyme complex yield lower nitrite and nitrate levels than those quantified with AChE-ACh complex [4,14].

We verified decreased amounts of GSNO and peroxynitrite inside erythrocytes when, on its membrane, AChE-ACh active complex was present, in relation to the values obtained when the inactive complex ACh-VM is formed [14]. Lower GSNO concentration in erythrocytes may result from lower glutathione (GSH) content. Reduced free GSH inside RBCs can be a consequence of lower reduced potential in the form of nicotinamide adenine dinucleotide phosphate concentration, a biomarker of the lower oxidative phase of phosphopenthose pathway; or from the existence of GSNO efflux from erythrocytes. We have shown that no variations are induced by both AChE-ACh and ACHE-VM complexes in glucose-6-phosphodehydrogenase, glyceraldehyde-3-phosphate dehydrogenase enzyme activities neither on 2,3- bisphosphoglycerate and L-lactate concentrations [14].

We are the former to measure GSNO liberated by erythrocytes in the presence of ACh [5]. So, the complex AChE-ACh induces GSNO efflux and contributes to lower the levels inside erythrocyte in relation to those obtained with the inactive complex AChE-VM [5,14].

When changes on AChE molecular conformations were induced by antibodies against the C or N terminus decreased amounts of GSNO and NO efflux from erythrocytes were obtained [13].

The variation of erythrocyte NO efflux, peroxynitrite and GSNO levels observed in the presence of velnacrine and ACh called our attention to investigate the NO metabolism in a set of redox status modulation. At that time, we studied the effects of dithiothreitol (DTT; a thiol reducing compound) to function as a thiol (SH) donor. It is known that SH groups are easily kept in the reduced state once a second thiol is added, such as cysteine or glutathione because they rapidly exchange disulfide groups. RBCs in the presence of DTT show significantly internal NO dependent reactions originating an increase in nitrite, nitrate and GSNO concentrations and a decrease on the NO efflux from erythrocytes. Peroxynitrite levels remained unchanged with AChE-ACh or AChE –VM enzyme complexes in the presence of DTT, but the levels of nitrite and nitrate molecules decreased. Significantly increased peroxynitrite concentrations were found in RBCs AChE-VM plus DTT 1µM and plus DTT 50 µM but lower plus DTT 10 µM [16]. We concluded that dithiothreitol induces activation of erythrocyte thiol status by decreasing NO efflux and allowing intracellular NO mobilization into different derivative molecules, both in the absence and presence of the AChE-ACh and AChE-VM enzyme complexes [16].

Beyond the hemostasis properties of fibrinogen (Fib), this protein is a hemorheological promoter of RBCs aggregation and plasma viscosity [17]. Fibrinogen is also known as one of the acute phase protein associated with inflammatory conditions [18]. Fib binds to erythrocyte CD47 and at a normal range of concentrations is able to decrease NO efflux [19,20].

But high levels of Fib, observed in inflammatory diseases, have shown an increase in NO efflux from RBCs in dependence of the band 3 protein phosphorylation and lower levels of cAMP [20] (Figure 1).

Figure 1: Representative diagram of normal NO efflux from erythrocyte in an in vitro model of hyperfibrinogenemia. Fibrinogen (Fib) binds to CD47. It was shown that the amount of NO efflux is increased at lower adenosine monophosphate (cAMP) and normalized at high cAMP levels achieved in presence of forskolin and wortamannin (WORT), respectively activator of adenylyl cyclase and inhibitor of phosphodiesterase (PDE3).

Previously we verify an increased AChE enzyme activity in patients with glaucoma under timolol maleate therapy for reducing increased intra-ocular pressure and we evidenced that timolol is a weak inhibitor of erythrocyte AChE [21]. When the less active complex AChE-timolol is formed in erythrocytes obtained from healthy donors, lower NO efflux and lower S-GSNO levels in erythrocytes compared with the active complex AChE-ACh were found [22]. The RBCs of glaucoma patients without timolol therapy are able to liberate the same amount of NO and have equal GSNO levels that are obtained after incubation with timolol [23].

Erythrocyte NO availability as a marker of inflammatory vascular diseases

When the less active complex AChE-timolol is formed in erythrocytes obtained from glaucoma patients higher NO efflux and GSNO content were observed in relation to those assessed in RBCs from healthy humans [23]. In this painful and progressive ocular disease the decrease ability to preserve NO inside the RBCs may be a deleterious nitrogen reactive species contributing to worse the vascular endothelial dysfunction.

In two groups of patients’ one with systemic lupus erythematosus and the other with rheumatoid arthritis, characterized by subclinical atherosclerosis, the NO efflux values obtained from their erythrocytes associate negatively with carotid intima-media thickness (cIMT) and with the presence of plaques and NO efflux is an independent predictor of cIMT [24]. In these immune diseases NO may be considered a primary nitrogen reactive species resulting from its rescue inside the RBCs.

Another painful and mortal disease in small years after appearance with very rare exceptions is amyotrophic lateral sclerosis (ALS) [25]. RBCs of these patients showed higher AChE enzyme activity, lower nitrite concentrations and lower NO efflux from RBCs than those obtained in healthy humans; higher NO quartiles values associated with worse respiratory function; positive relation between quartile values were obtained between AChE enzyme activity and nitrites [25]. The discrepancy between the active state of AChE enzyme and lower NO efflux observed in the blood samples of the ALS patients must be explored in future studies. But we hypothesized that these biochemical parameters can be considered as biomarkers of ALS disease [25].

Also in sepsis, some studies have regarded the erythrocyte NO availability. But besides a lot of research that has been done in all classes of sepsis it is insufficient due to the high level of mortality of this disease. We verify in a follow-up study conducted in an intensive care unit (ICU) that patients with septic shock, that died, showed higher efflux of NO from RBCs than the survivors. The NO may combine with oxygen anion peroxide produced by the dysfunctional vascular endothelium originating peroxynitrite; this is a secondary nitrogen reactive species with deleterious effects on all blood components and a marker of inflammation. Moreover, blood flow and high microvascular flow index were observed in those septic patients before dead with a device to follow and measured the hemodynamic parameters in sub-lingual microcirculation [26].

Conclusions

The erythrocyte nitrogen reactive species were evidenced to be dependent on circulating acetylcholine, fibrinogen and inhibitors of acetylcholinesterase, redox thiol status, protein degree phosphorylation and cAMP levels. Erythrocyte NO efflux and AChE may be considered as biomarkers of inflammatory vascular diseases.

Acknowledgments

This work was funded by Fundação para a Ciência e Tecnologia: LISBOA-01-

0145-FEDER-007391, project cofunded by FEDER, through POR Lisboa 2020 - Programa Operacional Regional de Lisboa, PORTUGAL 2020. The authors thanks Teresa Freitas and Emilia Alves for their technical and type-writing support respectively.

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