Endothelial cell expression of hemoglobin α regulates nitric oxide signaling

Abstract

Models of unregulated nitric oxide (NO) diffusion do not consistently account for the biochemistry of NO synthase (NOS)-dependent signaling in many cell systems 1,2,3 . For example, endothelial NOS (eNOS) controls blood pressure, blood flow and oxygen delivery through its effect on vascular smooth muscle tone 4 , but the regulation of these processes is not adequately explained by simple NO diffusion from endothelium to smooth muscle 3,5 . Here, we report a new paradigm in the regulation of NO signaling by demonstrating that hemoglobin (Hb) α is expressed in arterial endothelial cells (ECs) and enriched at the myoendothelial junction (MEJ), where it regulates the effects of NO on vascular reactivity. Surprisingly, this function is unique to Hb α and abrogated by its genetic depletion. Mechanistically, endothelial Hb α heme iron in the Fe3+ state permits NO signaling, and this signaling is shut off when Hb α is reduced to the Fe2+ state by endothelial cytochrome B5 reductase 3 (CytB5R3) 6 . Genetic and pharmacological inhibition of CytB5R3 increases NO bioactivity in small arteries. These data reveal a novel mechanism by which the regulation of intracellular Hb α oxidation state controls NOS signaling in non-erythroid cells. This paradigm may be relevant to heme-containing globins in a broad range of NOS-containing somatic cells 7,8,9,10,11,12,13 . Endothelial NOS modulates blood vessel diameter in response to both vasodilators and vasoconstrictors. For example, it is known that during arterial constriction NO from endothelium feeds back on smooth muscle to control the magnitude of the response to a vasoconstrictor (e.g. phenylephrine (PE)) 5,14 . PE stimulation of thoracodorsal (TD) arteries ex vivo - and of primary human ECs and vascular smooth muscle cells (SMCs) in the vascular cell co-culture (VCCC) model - reproduced classical NOS- and cGMP-dependent changes in SMC biology (Supplementary Fig. 1a–d). However, NO did not diffuse into the extracellular space (Supplementary Fig. 1e–h), consistent with our previous work showing compartmentalized NOS signaling at the MEJ, the critical EC-SMC contact point in the TD and other small arteries and arterioles 5 . Therefore, we studied MEJ proteins that could contribute to local regulation of NO diffusion and biochemistry. We performed a proteomic analysis of MEJs isolated from VCCCs using the isobaric tags for relative and absolute quantitation (iTRAQ) system (Supplementary Fig. 2). Surprisingly, Hb α was abundant at the MEJ (Supplementary Fig. 3). Because Hb can regulate NO diffusion and biochemistry in erythrocytes 15,16 , we hypothesized that it could have a similar function at the MEJ. First, we confirmed the proteomic data using immunoblot and immunofluorescence. We demonstrated Hb α protein expression in the VCCC model but no expression of Hb β (Fig. 1a). There was little Hb α expression in human ECs or SMCs grown separately, and there was no Hb α in the fibronectin or gelatin used to coat the VCCC transwells (Fig. 1a). Next, we confirmed these results in co-cultures of different types of ECs and SMCs where MEJs also expressed abundant Hb α (Supplementary Fig. 4). We then studied the MEJ distribution of Hb α in situ. Gold particles labeling Hb α were abundant in the MEJ of mouse TD arteries visualized by transmission electron microscopy (TEM) (Fig. 1b). In contrast, carotid arteries – conduit arteries which have few MEJs - expressed little Hb α as observed by TEM (Fig. 1b), immunoblot (Fig. 1c), and immunofluorescence (Fig. 1d). These data were consistent in human skeletal muscle arterioles (Fig. 1d) and throughout multiple tissue beds (Supplementary Fig. 5). Using en face immunofluorescence, we found punctuate Hb α staining primarily at paracellular junctions of TD – but not carotid – arteries, whereas little Hb β was observed (Fig. 1e). Chemical crosslinking analysis revealed that the Hb α was monomeric in TD arteries and the VCCC (Fig. 1f). Next, we measured Hb α mRNA using real-time PCR (Fig. 1g) and established that ECs transfected with Hb α siRNA had decreased protein expression at the MEJ (Supplementary Fig. 6a) and in the monolayer (Supplementary Fig. 6b). Loss of Hb α protein expression did not affect eNOS expression in the EC monolayer (Supplementary Fig. 6b) or at the MEJ (Supplementary Fig. 7). Transcripts for other globins including myoglobin, neuroglobin and cytoglobin were absent in ECs (Supplementary Fig. 8a–c). Only cytoglobin mRNA and protein were expressed in SMCs (Supplementary Fig. 8c–d), consistent with a previous report 11 . In addition, we also found Hb α stabilizing protein in the endothelium of TD arteries and in the VCCC (Supplementary Fig. 9a–b). Taken together, these data show for the first time that arterial ECs express Hb α mRNA and protein and are responsible for enriched Hb α expression at the MEJ. To investigate the functional role of Hb α in ECs and its effect on eNOS signaling, we transfected ECs in isolated TD arteries with Hb α or control siRNA. Knockdown efficiency was 70–80% (Supplementary Fig. 10). Loss of Hb α resulted in a dramatic loss in arterial reactivity following PE application in a single or cumulative doses (Fig. 2a–b) and increased reactivity to acetylcholine (Ach) (Fig. 2c), but there was no change in response to 5-hydroxytryptamine (5-HT) (Supplementary Table 1). EC50 and Emax values are in Supplementary Table 2. We observed no difference in basal tone (Supplementary Fig. 11a). However, with the addition of the NOS inhibitor L-N G –nitroarginine methyl ester (L-NAME), the effect of Hb α siRNA was comparable to control conditions for both PE and Ach responses (Fig. 2a–c). We thus hypothesized that eNOS, the primary isoform in the vessel wall, may be in close spatial proximity to Hb α. We tested this hypothesis using four methods: co-localization studies by immunofluorescence (Fig. 2d, g), a proximity ligation assay (Fig. 2e), and co-immunoprecipitations from cell lysates (Fig. 2f, h) and purified proteins (Fig. 2i). These analyses revealed Hb α and eNOS are in a macromolecular complex and can form a direct protein-protein interaction. Hb α likely interacts with eNOS to regulate blood vessel tone by controlling NO diffusion through its scavenging by heme iron 13,17,18,19 . We studied the mechanism of interaction by measuring loss of NO radical in TD and carotid arteries, and in the VCCC model. NO was lost in TD arteries, but not carotid arteries; and it was lost in MEJ fractions - but not EC or SMC -lysates (Supplementary Fig. 12a–b). Next, we knocked down endothelial Hb α in isolated arteries (Fig 2j) or VCCCs (Fig 2l) using siRNA. Loss of Hb α increased NO diffusion across the vessel wall (Fig. 2k) and in the VCCC (Fig. 2m). Together, these results indicate that endothelial Hb α can regulate arterial tone through its effects on NO diffusion. Next, we hypothesized that Hb α heme iron in the oxygenated Fe2+ state should control NO diffusion through a fast reaction (2.4 x107 M−1·sec−1) 20 resulting in dioxygenation 21,22 , whereas Fe3+ state should permit NO diffusion due to a slower reaction rate (3.3 × 103 M−1·sec−1) 23 . We found that Hb α heme iron resides in both states. First, using UV-visible spectroscopy, we identified a Soret peak (~420 nm) and Q bands (~540–575 nm) in isolated TD arteries consistent with oxygen bound Hb Fe2+, whereas there was no peak in carotid arteries (Fig 3a). Next, we measured the oxidation state of Fe and found approximately 42% existed in the Fe2+ and 58% in the Fe3+ state (Fig. 3b). These measurements were sensitive to Hb α siRNA (Fig. 3b). Consistent with this observation, we found that carbon monoxide (CO) ligated Fe2+ heme, resulted in increased NO diffusion across isolated vessels (Supplementary Fig. 12c). When MEJ fractions were studied, we found a Soret peak (~410 nm) characteristic of the Fe3+ state (methemoglobin) (Fig. 3c). Interestingly, pelleted membranes from MEJ fractions were dark brown, consistent with Fe3+ oxidation (Supplementary Fig. 13). We found approximately 32% of Fe existed in the Fe2+ and 68% in the Fe3+ state (Fig. 3d), results that were also sensitive to Hb α siRNA (Fig 3d). We also observed an increase in NO diffusion in VCCCs treated with CO (Supplementary Fig. 12d). Previous work has demonstrated that NO-heme Fe3+ interaction results in reductive nitrosylation, a mechanism known to generate S-nitrosothiols, which we have shown to be critical for gap junction regulation at the MEJ 5,24,25 . Using N-acetylcysteine as a bait reactant on the abluminal side (Supplementary Fig. 14a, c), we also found a striking loss of S-nitrosothiol synthesis after Hb α knock down in TD arteries (Supplementary Fig. 14b) and in the VCCC (Supplementary Fig. 14d). Together, these results suggest that Hb α heme oxidation state regulates both NO diffusion and bioactivation. Next we determined the mechanism regulating Hb α oxidation state. In erythrocytes, cytochrome B5 reductase 3 (CytB5R3) or diaphorase 1, a known methemoglobin reductase, controls the heme iron oxidation state through reduction of Fe3+ 6. Using immunofluoresence (in vivo Fig 4a, in vitro Fig. 4e), TEM (Fig. 4b), and Western blot analysis (in vivo Fig. 4c, in vitro 4d), we identified that CytB5R3 was expressed in ECs and at the MEJ. In addition, we established CytB5R3 is in a complex with Hb α using four separate assays: immunofluorescence (Fig. 4f–g), proximity ligation assay (Fig. 4h), and co-immunoprecipitation from cell lysates and purified proteins (Fig. 4i). Indeed, molecular modeling of the crystal structures for Hb α, eNOS, and CytB5R3 revealed a discreet region of high probability where the proteins could interact (Supplementary Fig. 15). Next, we used CytB5R3 siRNA (knockdown efficiency: ~50%, Supplementary Fig. 16a) and overexpression to show that CytB5R3 regulates metHb α reduction. Time lapse UV-visible spectrometry demonstrated that loss of CytB5R3 inhibited metHb α reduction and that overexpression enhanced metHb α reduction (Supplementary Fig. 16b–c). To determine if CytB5R3 expression or activity regulates arterial tone, we tested both siRNA directed against endothelial CytB5R3 in TD arteries and a pharmacological inhibitor of CytB5R3, propylthiouracil (PTU) 26 . Knockdown efficiency was about 70% (Supplementary Fig. 17a). We observed a decrease in arterial reactivity in TD arteries transfected with CytB5R3 siRNA after PE stimulation with a single dose or cumulative concentrations (Fig. 4j–k) and increased reactivity with ACh dose response (Fig. 4l). Vascular reactivity to PE or Ach in TD arteries pretreated with PTU is shown in (Supplementary Fig. 18a–c). The effect with PTU was not reversible with L-thyroxine supplementation after PE stimulation (Supplementary Fig. 18b, inset). However, we found no change with 5-HT (Supplementary Table 1). EC50 and Emax values are in Supplementary Table 2. However, with the addition of L-NAME, the effect of CytB5R3 siRNA was comparable to control conditions (Fig. 4j–l) or PTU treated arteries (Supplementary Fig. 18a–b), results that were consistent with Hb α knockdown. We found no difference in basal tone for CytB5R3 siRNA or PTU (Supplementary Fig. 11a–b). Next we tested the effect of CytB5R3 on NO diffusion in vessels and VCCC (Fig. 4m, o). Knockdown of CytB5R3 siRNA was ~30% at the MEJ (Supplementary Fig. 17b) and in the EC monolayer but not in SMCs (Supplementary Fig. 17c). Both CytB5R3 siRNA and PTU treatment increased NO diffusion across both isolated vessels and in VCCC (Fig. 4n, p; Supplementary Fig. 18d–g). Note that CytB5R3 knockdown did not alter MEJ eNOS or Hb α expression (Supplementary Fig. 17d). We conclude that EC expression of Hb α plays a critical role in the regulation of NOS-mediated signaling and in the control of arterial vascular reactivity. These results may have far reaching implications that could influence many aspects of vascular biology and disease. For example, endothelial Hb α expression may participate in blood pressure control, arteriogenesis and anti-inflammatory signaling, as well as impact other redox signaling molecules (e.g. superoxide and hydrogen peroxide). Indeed, our results correlate with diagnostic indices for human alpha thalassemia major (Hb α −/ − −/ −) fetuses, who show increased cerebral blood flow during development 27 . Furthermore, these observations may help to explain why inhibition of CytB5R3 attenuates hypertension 28 and may suggest that CytB5R3 is a novel therapeutic target for disease treatment. However, studies devoted toward understanding the mechanisms of CytB5R3 regulation and its interaction with Hb α will need to be clarified. More broadly, somatic cell types as diverse as alveolar epithelial cells 7 , macrophages 9 , neurons 10 and renal mesangial cells 8 express both Hb and NOS. It is thus possible that Hb could regulate NO signaling pathways relevant to many cell and organ systems. Taken together, these data provide evidence for a novel paradigm in which somatic cell Hb oxidation is required for NO-dependent bioactivity. Methods Summary Human coronary ECs and SMCs were co-cultured and fractionated as previously described 29 . iTRAQ proteomic screening was used to identify and quantify proteins enriched at the MEJ as previously demonstrated 30 . Protein was analyzed using Western blot, immunofluorescence, and immuno TEM, while mRNA was measured using real-time-PCR. Isolated TD arteries were cannulated, pressurized and stimulated with PE or Ach as previously shown 5 or perfused with anaerobic aqueous nitric oxide. Detailed methods can be found in supplementary materials and methods. Supplementary Material 1