Key Points
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We characterized and classified the membranous particle content of apheresis PLTs for transfusion during their storage.
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After 7 days storage, the amount of degranulated PLTs, PLT membrane ghosts, and vesicles produced by apheresis PLTs increases.
Visual Abstract
Abstract
Platelets (PLTs) for transfusion can be stored for up to 7 days at room temperature (RT). The quality of apheresis PLTs decreases over storage time, which affects PLT hemostatic functions. Here, we characterized the membranous particles produced by PLT storage lesion (PSLPs), including degranulated PLTs, PLT ghosts, membrane fragments, and extracellular membrane vesicles (PEVs). The PSLPs generated in apheresis platelet units were analyzed on days 1, 3, 5, and 7 of RT storage. A differential centrifugation and a sucrose density gradient were used to separate PSLP populations. PSLPs were characterized using scanning and transmission electron microscopy (EM), flow cytometry (FC), and nanoparticle tracking analysis (NTA). PSLPs have different morphologies and a broad size distribution; FC and NTA showed that the concentration of small and large PSLPs increases with storage time. The density gradient separated 3 PSLP populations: (1) degranulated PLTs, PLT ghosts, and large PLT fragments; (2) PEVs originated from PLT activation and organelles released by necrotic PLTs; and (3) PEV ghosts. Most PSLPs expressed phosphatidyl serine and induced thrombin generation in the plasma. PSLPs contained extracellular mitochondria and some had the autophagosome marker LC3. PSLPs encompass degranulated PLTs, PLT ghosts, large PLT fragments, large and dense PEVs, and low-density PEV ghosts. The activation-related PSLPs are released, particularly during early stage of storage (days 1-3), and the release of apoptosis- and necrosis-related PSLPs prevails after that. No elevation of LC3- and TOM20-positive PSLPs indicates that the increase of extracellular mitochondria during later-stage storage is not associated with PLT mitophagy.
Introduction
Apheresis platelets (PLTs) can be stored for 7 days at ambient temperatures, in a range from 20 to 24°C, under constant gentle agitation,1 conditions that lead to PLT storage lesion (PSL).
PSL is a term first introduced by Murphy and Gardner2 to describe deleterious changes observed in PLTs during storage, such as an increase in lactate levels, decrease in pH, loss of surface membrane glycoproteins, particularly glycoprotein Ib, and reduced aggregation responses to adenosine diphosphate and collagen. Storage lesion limits the apheresis PLT shelf-life and is associated with decreased in vivo PLT recovery, survival, and hemostatic activity after transfusion.3,4
The mechanisms responsible for PSL are multifactorial and include the physical stress from PLT collection, processing, storage, and manipulation after collection.5,6 Aside from the physical stresses, biochemical changes due to apheresis PLT aging contribute to PSL.7
Although anucleate, PLTs have the capacity to undergo programmed cell death.7, 8, 9, 10, 11 During storage, PLTs present several features of apoptosis,12, 13, 14 such as cytoskeletal disruption, vesiculation, caspase activation, and phosphatidylserine (PS) exposure.12
Biochemical processes associated with PSL have also been linked to PLT necrosis,15 particularly those responsible for severe mitochondrial damage, swelling of plasma and organelle membranes, changes in intracellular pH, membrane lysis and release of lactate dehydrogenase, and loss of sialylated glycans.16, 17, 18, 19 In fact, the possibility of stored platelets undergoing secondary necrosis may partly explain the inability of apoptosis inhibitors to maintain the viability of stored PLT products.7
Autophagy is another operational programmed cell death pathway in PLTs.20 Autophagy is induced upon PLT activation and is essential for hemostasis and thrombosis,21 and mitophagy in PLTs has been demonstrated in hypoxic conditions,22 diabetes,23 and starvation.24 However, the contribution of autophagy/mitophagy to the PSL remains to be established.
The biological effects of the releasates in the apheresis PLT supernatant are a current topic of research.25 For instance, Cognasse et al demonstrated that the supernatants of stored PLTs contain potential immunomodulatory factors,26 and Sut et al showed that platelet concentrate supernatants alter endothelial cell messenger RNA, causing cell activation.27 In those studies, attention was given to the soluble molecules present in the apheresis PLT supernatants, such as cytokines, chemokines, and so on. In this study, we investigated membranous particles that are products of PSL (PSLPs), including degranulated PLTs (DPLTs), PLT ghosts (empty platelet plasma membranes, free of granules, other organelles, and cytoplasmic content), membrane fragments, and PLT extracellular membrane vesicles (PEVs). The fate of particles in circulation, including cellular uptake, depends on the particle size and surface properties.28, 29, 30, 31, 32, 33 Thus, the physicochemical features of circulating PSLPs are expected to influence their interactions with cells of the vascular system and, consequently, their ability to transfer bioactive cargo molecules.34,35
Materials and methods
Texas Red 1,2-dihexadecanoyl-sn-glycero-3-phosphoethanolamine (DHPE) was from Thermo Fisher Scientific. Fluorescein isothiocyanate (FITC)-conjugated LC3 antibody kit (no. FCCH100171, clone 4E12), bovine serum albumin, prostaglandin E1, 1,6-diphenyl-1,3,5-hexatriene (DPH), and sucrose were from Sigma. Anti-human Tom20 (F-10) Alexa Fluor 647-conjugated (no. sc-17764 AF647) was from Santa Cruz Biotechnology. FITC mouse anti-human CD41a (clone HIP8), phycoerythrin (PE) mouse anti-human CD41a (clone HIP8), PE mouse anti-human CD62P (clone AK-4), PE-conjugated mouse immunoglobulin G1 (IgG1; clone MOPC-21; isotype control), and FITC-conjugated mouse IgG1 (clone MOPC-21; isotype control) were from BD Pharmingen. Lactadherin-FITC Labeled (BLAC-FITC) was from Haematologic Technologies. Osmium tetroxide, paraformaldehyde, glutaraldehyde, and Embed 812 were from Electron Microscopy Sciences.
Collection and storage of apheresis PLTs
Apheresis PLTs from 12 healthy donors (1 110 000 ± 168 000 platelets per μL) were collected using an Amicus cell separator (Fresenius Kabi) and provided by the Department of Transfusion Medicine, National Institutes of Health (Bethesda, MD). The platelet units were procured by the Center for Biologics Evaluation and Research institutional review board, which allows only the release of deidentified material. All units were collected and stored in plasma at room temperature (RT; 20 to 24°C) on a PF48h Horizon Series Platelet Agitator (Helmer Scientific; flatbed platelet agitator, agitation speed 60 cycles/min, stroke length 3.8 cm) for 7 days with continual side-to-side motion.
Isolation of PSLPs
From apheresis PLT units, 5 mL samples were collected on days 1, 3, 5, and 7 of storage; prostaglandin E1 with a final 1μM concentration was added to the PLT samples before centrifugation at 1000 g for 30 minutes at RT to isolate intact PLTs from the supernatant containing PSLPs.
Flow cytometry
The supernatant containing PSLPs was diluted with 1.5% bovine serum albumin/phosphate-buffered saline (PBS) to get 1000 to 2000 events per second during analysis. Then, 300 μL of diluted supernatant was incubated for 20 minutes at RT with a saturating concentration of monoclonal antibodies against CD41a (FITC/PE, 10 μL; 1:10), CD62P (PE, 10 μL; 1:10), TOM20 (Alexa 647, 10 μL; 1:5), LC3 (FITC, 5 μL), or lactadherin (FITC, 10 μL; 1:5), or with the membrane labeling DHPE (Texas Red, 20 μL; 1:10). PSLPs were sedimented at 30 000 g for 30 minutes at 4°C and washed with 1 mL of PBS. The pellet was resuspended in 300 μL of PBS and immediately analyzed using an LSRII flow cytometer (BD Biosciences). Respective IgG isotype antibody controls and nonlabeled samples were used as controls. To estimate the size of PSLPs, the flow cytometer was calibrated using the ApogeeMix calibration beads (Apogee Flow Systems). TruCount TM beads (Becton Dickinson) were used to evaluate the flow rate and PSLP counts. Data analysis was performed using FlowJo software. All the antibodies were titrated to ensure a saturating concentration, and we analyzed at least 10 000 gated PSLPs for each sample.
Sucrose density gradient
PSLPs pelleted from 100 mL of apheresis PLT units were subjected to a sucrose density gradient. Sucrose gradients were prepared in 10 mL Beckman centrifuge tubes in 1 mL layers of sucrose solution in tris(hydroxymethyl)aminomethane buffer (0.21, 0.46, 0.56, 0.73, 0.88, 1.02, 1.10, 1.22, 1.33, 1.46, 1.54, and 2.25 mol/L) to create a density (d) gradient of 1.0259 to 1.2575 g/mL. After ultracentrifugation (Beckman Counter) at 100 000 g for 14 hours, the 3 populations of PSLPs were collected and analyzed by flow cytometry (FC) by diluting 50 μL of each fraction in 1 mL of Tyrode buffer before incubation with antibodies. Fractions were also prepared for transmission electron microscopy (TEM).
Field emission scanning electron microscopy
Samples were fixed with 4% paraformaldehyde and 2% glutaraldehyde, followed by dehydration and drying at RT. Samples were sputter-coated with a thin film of gold. The change in morphology of platelets at different days of storage was evaluated by analyzing scanning electron microscopy (SEM) images using ImageJ software and calculating the circularity value (values 1.0-0.0 indicate a perfect circle to an increasingly elongated polygon shape).36
TEM
Samples were fixed with 2.5% paraformaldehyde and 2.5% glutaraldehyde, followed by 1% osmium staining; samples were dehydrated and resin-embedded before ultramicrotomy.
Fluorescence polarization
Apheresis PLTs were incubated with 1 μM DPH for 30 minutes. A total of 30 nmol/L of membrane fluidizer halothane was used as a positive control. The fluorescence of DPH was read at 360 or 420 nm.
TG test
Thrombin generation (TG) test was performed as described previously,37 using 0.2 pM tissue factor, pooled healthy plasma, CaCl2, and a fluorogenic Z-Gly-Gly-Arg-7-amino-4-methylcoumarin substrate.
Statistical analysis
FC data are expressed as the fold change in the count of small and large PSLPs normalized to that of day 1 of storage (mean ± standard error) (#P < .01; ∗P < .05; N = 12). FC data for the 3 PSLP populations isolated by sucrose gradient are presented as mean + standard deviation. The results were calculated from at least 3 independent experiments; FP data are presented as mean + standard deviation. One-way analysis of variance was used; P values < 0.05 were considered significant.
Results
Characterization of apheresis PLTs after 1 to 7 days of storage
To characterize the PSLPs present in apheresis PLT products, apheresis PLT units were collected and stored at RT under gentle agitation for up to 7 days, according to standard guidelines.38,39 Centrifugation of apheresis PLTs at 1000 g for 30 minutes allowed separation of intact PLTs for the characterization of the supernatant containing the PSLPs.
The effect of RT storage on apheresis PLT morphology was analyzed by electron microscopy. SEM topographic images (Figure 1A,C,E,G) and calculated circularity values (Figure 1J) of apheresis PLTs at different days reveal that aging apheresis PLTs undergo shape changes that include pseudopodia formation, membrane fragmentation, and PEV release; those observations were confirmed by TEM ultrastructural images (Figure 1B,D,F,H). TEM shows the presence of apoptotic (blebbing and filopodia extrusion) and necrotic (fragmented membrane release of intracellular organelles) PLTs, especially on days 5 and 7 of storage.
The physical state of apheresis PLT membranes during storage was evaluated by fluorescence polarization (FP) of the DPH probe,40 shown in Figure 1I. RT storage causes disruption of membrane lipid packing, as indicated by the observed increase in membrane fluidity (or decrease in viscosity).
PSLP amount increases while PLTs are being stored
The number of PSLPs in the apheresis PLT supernatant increases with storage time, as measured by Coulter counting (Figure 2A) and FC (Figure 2B). Although the Coulter counter detects only large PSLPs, FC demonstrates that PSLPs have a broad size distribution that ranges from 200 nm to 5 μm. Figure 2C shows a representative forward scatter (FSC) histogram plot of PSLPs from PLT supernatant on day 5 of storage overlapped with the FSC histogram plots of silica standard size particles. As shown in Figure 2B, 2 major PSLP populations were identified and gated at the FSC peak of the 880 nm silica particles for further FC data analysis. Figure 2D-E show a steady increase in PS+ and PS+CD41+ PSLPs in both small PSLP (200-880 nm) and large PSLP (880 nm-5 μm) populations with storage time. The number of large PS+CD62P+ PSLPs also increases with storage time. However, the number of small PS+CD62P+ PSLPs increases from day 1 to day 3 of storage only. Nanoparticle tracking analysis confirmed the elevation of PSLP concentration during storage (Figure 2F-G).
The morphologies and broad size distribution of the PSLPs are demonstrated by SEM images of apheresis PLT supernatants from days 1, 3, 5, and 7 of storage, presented in Figure 3A, B, C,D, respectively.
PSLPs are highly diverse by their density and morphology
For further characterization, PSLPs isolated from apheresis PLT supernatant on day 7 of storage were pelleted by centrifugation at 30 000 g for 20 minutes and subjected to a sucrose density gradient at 100 000 g at 4°C for 14 hours. As shown in Figure 3., Figure 4.A, 3 major populations of PSLPs were isolated and imaged by TEM. Figure 4B is a representative image of the denser PSLP population collected at d = 1.14-1.17 g/mL band, which is composed of partially DPLTs and large electron-dense PEVs; the membranes of the some DPLTs are fragmented, and release of intracellular organelles is observed. Figure 4C is a representative image of the population collected at d = 1.09-1.13 g/mL band composed of large and electron-dense PEVs with and without intact membranes. Figure 4D represents the population collected at the top layer of the sucrose gradient, composed of electron-translucent vesicles with a very low-density (d = 1.02-1.06 g/mL band).
The PSLP populations isolated by the density gradient were labeled for PS, CD41a, and CD62P and analyzed by FC. Figure 5A shows that on day 7 of storage, most of the ghost PSLPs are <700 nm (Figure 5A) and that the denser PSLPs are composed of 2 population with size ranges of 200 to 700 nm and 700 nm to 5 μm, as compared with silica standard size particles. Figure 5D shows that the number of PS+CD41a+ PSLPs and PS+CD62P+ PSLPs increases with the population density.
To verify the presence of PS on the PSLP surface, which is relevant for procoagulant activity, TG assay was performed. All PSLP populations isolated by the sucrose gradient are procoagulant. The TG activity was inhibited by blocking PS by adding 10 μM lactadherin (Figure 5E-F). We demonstrated strong inhibition of TG by lactadherin; however, in the case of dense PEVs, a little residual PS was still present in the system, likely indicating that the lactadherin concentration was not high enough to block all PS on the large membrane surface area of the dense PEV preparation. supplemental Figure 1 shows that at least 97% of PSLPs label for PS. PSLPs with disrupted membranes allow for lactadherin binding to PS in the inner membrane leaflet.
Apheresis PLTs release mitochondria during storage
The release of mitochondria (MITO) by apheresis PLTs during storage was indicated by TEM. Figure 6A, a representative TEM image of apheresis PLTs stored for 7 days, shows extracellularly enlarged MITO with irregular cristae structures. FC analysis of PSLPs labeled with the mitochondrial marker TOM20 shows that the number of PS+TOM20+ PSLP count increases with storage time, as shown in Figure 6C. The TEM image presented in Figure 6B clearly shows ongoing mitophagy on apheresis PLTs on day 3 of storage. To evaluate the role of autophagy/mitophagy on the release of MITO during storage, PSLPs were labeled with the autophagosome marker LC3. Figure 6C indicates the presence of mitophagy associated PSLPs (TOM20+LC3+ PSLPs and DHPE+LC3+TOM20+ PSLPs), which do not significantly increase with storage time.
Discussion
Based on our observations and previously published work,41 we propose that the PSLP generation evolves from PLT activation, apoptosis, necrosis, and autophagy, as described in Figure 7. Although the release of PLT extracellular vesicles (membrane microparticles) during PLT storage for transfusion has been previously investigated, very few data exist about a structural analysis of all membranous products of PSL. This study is focused not only on PLT extracellular vesiculomes but also on the characterization of a complex spectrum of PSLPs, that is, the DPLTs, PLT ghosts, fragments, and other different PLT membranous particles present in the apheresis PLT products stored at RT for transfusion. This article excludes the protein particles that may form during apheresis PLT storage.
TEM is considered the gold standard technique to evaluate the morphological features of cell death,42,43 including autophagy.44 Here, TEM revealed that the number of apoptotic and necrotic PLTs in apheresis PLT products increases with storage time and that mitophagy is operational in stored PLTs. We propose that these cell death processes contribute to the PSLP formation during storage of apheresis PLTs.
Apheresis procedures and storage of concentrated PLTs in bags expose PLTs to several stress factors, including contact with artificial surfaces, chemical changes caused by anticoagulants and additive solutions, metabolic stress, and shear stress, which collectively induce PLT activation and signaling leading to PLT apoptosis.45 In agreement with that, our data show that stored PLTs undergo membrane remodeling, as evidenced by the increase in membrane fluidity and other structural changes (observed by electron microscopy) that are hallmarks of PLT activation: degranulation, pseudopodia formation, and PEV release.41,46 However, PSLPs are not composed only of PEVs from PLT activation during storage.
The density gradient allowed for the isolation of 3 major populations of PSLPs that are composed of DPLTs, PEVs, and PEV ghosts. TEM revealed that the DPLTs are PLTs with intact membranes that partially release the granule contents. DPLTs also include necrotic PLTs,15 that is, PLTs that lost some of the internal organelles due to membrane fragmentation as observed by TEM. The tendency of apheresis PLT membranes to undergo fragmentation was also indicated by the membrane fluidity assay; the observed increase in membrane fluidity suggests that PLT membranes are less organized and viscous and thus more susceptible to lysis.47 The large/dense PEV populations encompass the PEVs from PLT activation41 and organelles from the fragmented necrotic PLTs. PSLPs include the PEV ghosts isolated at the very low-density band, which are electron translucent. That indicates that the PEV ghosts are remnant PEVs after the release of their internal contents. TEM and SEM allowed visualization of PSLPs with fragmented membranes, especially after day 3 of storage. Aside from the shear stress, proteolysis is known to induce membrane destabilization and fragmentation.48 Indeed, extensive proteolysis in stored PLTs has been demonstrated,49 and it has been associated with apoptosis.50,51 In addition, FC analysis shows that the percentage of CD41a+ and CD62P+ in PEV ghosts is reduced as compared with in denser PEV and DPLT populations. Shedding of CD41a, CD62P epitopes due to proteolysis during storage has been reported previously.26,52 Noteworthy, PLT ghosts41 were also occasionally observed, indicating that the number of completely exhausted apheresis PLTs is relatively small during the storage up to 7 days.
FC analysis of PSLPs revealed 2 major PSLP populations distinguished by size distribution. Particle numbers of small and large PSLP populations steadily increase with storage time, as quantified by PS+ PSLPs and PS+CD41a+ PSLPs. The small PSLP population is composed of PEVs and PEV ghosts, as the sizes are <700 nm; the large PSLP populations are apoptotic and necrotic PLTs, PLT ghosts, and potentially other PSLP aggregates. Although we used well-established, relatively gentle methods for separation of platelets and PSLPs to minimize preanalytical platelet activation and alteration of PSLPs, we cannot fully exclude the impact of centrifugation and sucrose density gradient separation on PLT activation status and PSLP profile. Therefore, alternative PSLP separation methods should be explored in future studies.53,54
Interestingly, the number of small PS+CD62P+ PSLPs increases from days 1 to 3 only. Upon activation, platelet P-selectin (CD62P) is rapidly mobilized from α-granules to the platelet surface, a process that requires adenosine triphosphate. However, stored platelets experience a dramatic decrease in mitochondrial respiration, and adenosine triphosphate depletion initiates within the first 2 days of storage.55 Thus, a lack of further increase in PS+CD62P+ PSLP counts after day 3 of storage likely indicates a decline in PLT activation potency.
It has been shown that activated56 and stored PLTs57 release free MITO, and we showed previously that PLTs activated by the thrombin receptor activating peptide release MITO by different mechanisms.41 In this study, we observed that stored apheresis PLTs contain extracellular MITO with damaged cristae and swollen structures, as presented in apoptotic and necrotic cells.16, 17, 18,58 That is in agreement with a study by Perales Villarroel et al demonstrating that PLT storage time is associated with mitochondrial dysfunction and impaired PLT function.55 Our FC analysis of PSLPs shows an increase in PS+TOM20+ PSLPs, which refers to the free MITO released upon PLT activation and MITO released from necrotic PLTs. Because of the membrane fragmentation, the large PS+TOM20+ PSLPs stemming from necrotic PLTs, and their count steadily increases with the storage time.
We identified PEVs that are products of mitophagy (TOM20+LC3+ PEVs), possibly released through unconventional exocytosis of autophagic vacuoles.41,59 Interestingly, an increase in DHPE+TOM20+LC3+ PSLP counts during early storage was observed in 50% of donors, who all had lower PSLP counts on day 1 of storage. That indicates that longer storage does not increase mitophagy and that the release of the most of mitophagy-related PEVs exhausts by day 1 of storage.
In conclusion, we propose that the PSLPs are generated by multifactorial stress of PLTs, including contact, metabolic, and shear stress-induced PLT activation60 and consequent cross-connections61 with apoptosis,43,45,50,62 necrosis,7,15,63 and autophagy.21,23,24 It has been demonstrated that different types of agitation affect platelet storage lesions, including activation status and PEV release.64, 65, 66 Flatbed agitation, used in our study, is commonly used for platelet storage today but represents significantly higher shear stress for platelets, compared with slow (3 RPM) circulatory agitation.67 Further studies are needed to evaluate how different types of agitation affect the activation status of PLTs and the quantitative profile of PSLPs, particularly PEVs. More gentle circulatory agitation should be investigated in this respect.
Our results suggest that different types of PSLPs are formed from functionally stimulated platelets and dying platelets. The activation-related PSLPs, including PEVs, are released particularly during the early stages of storage (days 1-3) and the release of apoptosis- and necrosis-related PSLPs prevails after that. A major challenge for the future will be the development of techniques to accurately analyze the contribution of distinct cell death pathways to PSLPs. The impact of these different PSLP populations on vascular endothelial cells and other relevant blood cells warrants future investigation. Although our study characterizes the morphology of the PSLPs in detail, further studies are needed on platelet storage-induced morphological and phenotype changes with the rate of their clearance from circulation and how different populations of PSLPs contribute to the hemostatic efficacy of transfused PLT units.
There are no ultimate data available on how PLT changes due to storage lesions affect their clinical transfusion performance. It has been shown, however, that administration of fresh PLTs, less than 2 to 3 days stored, was associated with a significant increase in corrected count increment compared with older PLTs in 7 out of the 8 studies, although (except 1 retrospective study) there was no impact on bleeding events.68 For full understanding of the biological effects of different PSLPs in circulation, in vivo studies in animal models would be useful. Activation, necrotic, and apoptotic PLT changes observed in our and other studies during storage well explain the decrease in in vivo bioavailability (recovery/survival) of longer-stored PLTs after transfusion. In contrast, observed procoagulant phenotype of longer-stored PLTs and the formation of procoagulant PSLPs support the hemostatic clinical efficacy of longer-stored platelets, which is in accord with the lack of an increase in bleeding complications with the time of PLT storage. The impact of these different PSLP populations on vascular endothelial cells and other relevant blood cells warrants future investigation to translate our findings into functional and clinical applications and to fully understand the functional significance of transfused PSLPs in vivo and their potential biomarker role in the evaluation of the quality of PLT transfusion products.
Conflict-of-interest disclosure: The authors declare no competing financial interests.
Acknowledgments
This project was supported in part by appointments to the Research Participation Program at the Center for Biologics Evaluation and Research administered by the Oak Ridge Institute for Science and Education through an interagency agreement between the US Department of Energy and the US Food and Drug Administration.
The findings and conclusions in this article have not been formally disseminated by the US Food and Drug Administration and should not be construed to represent any agency determination or policy.
Authorship
Contribution: M.P. wrote the manuscript and performed FC and fluorescent microscopy; S.H.D.P. wrote the manuscript and performed TEM, SEM, and density gradient; O.K.E. performed samples preparation and nanoparticle tracking analysis; I.D.T. performed membrane fluidity assay and edited the manuscript and figures; T.Z.T. performed TG assay; and J.S. supervised the project and revised the manuscript.
Footnotes
∗S.H.D.P. and M.P. contributed equally to this article.
Data are available on request from the corresponding author, Jan Simak (jan.simak@fda.hhs.gov).
The full-text version of this article contains a data supplement.
Supplementary Material
References
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