Abbreviations
BACKGROUND
Ischemia and reperfusion injury (IRI) is an inherent component of liver transplantation, resulting in severe complications such as primary nonfunction, ischemic-type biliary lesions, and postreperfusion syndrome.1 To overcome the increasing organ shortage, extended criteria donor (ECD) organs are frequently used to expand the donor pool. However, compared to standard criteria donor (SCD) organs, those organs are more sensitive to IRI and have higher risks of graft loss.2
A number of methods have been proposed to reduce IRI, such as ischemic preconditioning, pharmacological or gene interventions, and stem cell therapy.3 Recently, the efficacy and safety of various types of machine perfusion technologies for organ preservation have been tested, such as hypothermic (oxygenated) machine perfusion, subnormothermic machine perfusion, normothermic machine perfusion (NMP), and controlled oxygenated rewarming perfusion.4–11 Nevertheless, because grafts still suffer ischemia during procurement and implantation, those approaches are unable to completely abrogate the subsequent IRI.
To avoid graft ischemia entirely, we introduced an ischemia-free liver transplantation (IFLT) procedure. The procedure is designed to procure, preserve, and implant liver grafts under continuous NMP.12 In this study, we aimed to test how this procedure could change the biological consequences of graft IRI by analyzing serum and liver biopsy samples collected from the first nonrandomized controlled study.
METHODS
Study design
In our single-center, nonrandomized, controlled trial (ChiCTR-OPN-17012090), the efficacy, and safety were compared between IFLT and conventional liver transplantation (CLT). Liver biopsy samples were collected preprocurement (PP), at the end of preservation (EP) and one-hour postgraft revascularization (PR), and serum samples were collected postoperatively to evaluate the severity of graft IRI (Figure 1).
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Liver function tests
Blood samples were collected at 7 am each day for aspartate aminotransferase (AST), alanine aminotransferase (ALT), and total bilirubin (TBIL) measurement within 7 days posttransplantation. The detection was performed in clinical biochemistry laboratory of The First Affiliated Hospital of Sun Yat-sen University with Automatic Chemical Analyzer 7600-100 (Hitachi, Ltd, Tokyo, Japan).
Histological analysis
All liver samples were stored in 10% buffered formalin, immersed into paraffin, sliced (5 mm), and stained with hematoxylin and eosin (HE). Liver IRI was evaluated in a blinded manner by two pathologists by calculating the Suzuki score.13 When the scores were different, the pathologists engaged in a discussion and reached a final agreement. Samples were obtained from the first 14 IFLT cases and 14 randomly selected CLT cases.
Transmission electron microscopy
Liver tissues were soaked in 2.5% glutaraldehyde in 0.1 M phosphate buffer (pH = 7.2) for over 4 h at 4°C, dehydrated in graded solutions of ethanol for 10 min each time, and then infiltrated and embedded in resin to prepare ultrathin 70-nm sections. The sections were assessed using Transmission electron microscopy (TEM) (FEI Tecnai G2 Spirit Twin, Hillsboro, USA).
TdT-mediated dUTP nick end labeling assay
TdT-mediated dUTP nick end labeling (TUNEL) assays was conducted in accordance with the manufacturer's (Roche, 11684817910, USA) instructions to detected apoptosis. Samples were obtained from the first 14 IFLT cases and 14 randomly selected CLT cases. Apoptosis was quantified by TUNEL-positive cell number (mean ±SD), and Student's t-test was used for statistical analysis.
Superoxide dismutase and malondialdehyde levels
A portion of the liver tissue was homogenized in saline solution to analyze superoxide dismutase (SOD) and malondialdehyde (MDA) levels. The levels in samples were quantified with the relevant detection kits in accordance with the manufacturer's (Nanjing Jian-Cheng Bioengineering Institute, Nanjing, China) instructions.
Quantitative reverse transcription-polymerase chain reaction (RT-qPCR)
Total RNA extraction and cDNA synthesis were conducted as previously described,14 and quantitative reverse transcription-polymerase chain reaction (RT-qPCR) was conducted as the instruction of the SYBR Green Quantitative PCR kit (Takara Bio, Inc.). The related primer sequences are shown in Table S1. Relative mRNA expression was expressed by the 2–△△CT, and Student's t-test was used to evaluate significant differences.
Immunohistochemistry
Liver tissue paraffin sections were deparaffinized, performed for antigen retrieval, blocked endogenous peroxidases activity with 3% H2O2, and blocked with serum. The primary antibody was incubated for 2 h at 37°C. The secondary antibody was incubated for 30 min at room temperature. Following diaminobenzidine coloration, the slides were stained with hematoxylin for 3 min, costained with hematoxylin and coverslipped. Antibodies against von Willebrand factor (vWF) (Servicebio, GB11020) were purchased and used. Staining was assessed by pathologists who were blinded to the sample origins.
Immunoblot analysis
Tissue proteins harvested RIPA buffer (Fisher, Rockford, IL, USA) were prepared for separation in SDS-PAGE gel and then transferred to PVDF membranes (Bio-Rad). The membranes were blocked with 5% skim milk and incubated in the appropriate primary antibody, followed by incubation with a secondary antibody. The target protein bands were detected by a protein imaging system, Image Lab (ChemiDoc XRS+, BioRad, USA).
Enzyme-linked immunosorbent assay (ELISA)
The preparation of tissue supernatant and the detection of interleukin (IL)-1β and IL-18 was performed according to the instruction manual of enzyme-linked immunosorbent assay (ELISA) kits (Enzyme-linked Biotechnology Co., Shanghai, China). The absorbance of the samples was measured at 450 nm using a microplate reader, and the concentration of IL-1β and IL-18 was calculated according to the standard curve formula.
Metabolomics analysis
Liver biopsy samples were collected from the first 20 IFLT cases and 20 randomly selected CLT cases. The supernatant was prepared from 20 mg of liver tissue. A UHPLC system (1290, Agilent Technologies) was used to couple UPLC BEH Amide column (1.7 μm 2.1*100 mm, Waters) to TripleTOF 6600 (Q-TOF, AB Sciex and QTOF 6550 (Agilent) was performed by liquid chromatography-tandem mass spectrometry (LC-MS/MS). The LC/MS assay method and the database used for analysis were described in a previously published article.15 The in-house MS2 database was used for metabolite identification. The intrinsic variations of the data were illustrated by principal component analysis (PCA) and orthogonal projections to latent structure-discriminant analysis (OPLS-DA) score plots. Permutational multivariate analysis of variance (PERMANOVA) was used to assess differences in metabolite changes between groups. Variable importance plots (VIP) > 1 and p < 0.05 were used to distinguish significantly differentially abundant metabolites. The screening results of differential metabolites were visualized using a volcano plot. The enrichment analysis and topological analysis of the pathways were used to identify the key pathways related to the differentially expressed metabolites. The bubble plot shows the results of the metabolic pathway analysis.
Transcriptome analysis
Liver biopsy samples were obtained from the first 14 IFLT cases and 14 randomly selected CLT cases. The analysis was based on our previous publication.15 Genes greater than two-fold change and Padj < 0.01 between two groups were considered as differentially expressed. The raw data were uploaded to the NCBI Gene Expression Omnibus (GEO, accession number GSE113024).
Proteomics analysis
Protein was extracted from liver biopsies from 12 IFLT cases and 12 CLT cases at EP and PR. Protein from each sample was digested into peptides using MS-grade Tyrisin (Promega, Madison, WI). The peptides were resuspended in 0.1% formic acid aqueous solution, and iRT peptide was added. The mixed liquor was tested by on-line nanospray LC-MS/MS on an Orbitrap Fusion Lumos mass spectrometer (Thermo Fisher Scientific, MA, USA) coupled to an EASY-nanoLC 1200 system (Thermo Fisher Scientific). Direct data independent acquisition (DIA) analysis was performed on DIA data using Spectronaut 14 (Biognosys AG, Switzerland). The expression levels of proteins with greater than 1.5- or less than -1.5-fold changes and Padj < 0.05 were considered as differentially expressed. The Metascape and MetaCore online databases were used for enrichment analysis of differential proteins.
Cytokine/chemokine Luminex assay
Peripheral venous blood samples from 11 IFLT recipients and 14 CLT recipients were collected using EDTA as an anticoagulant at 12 h after graft revascularization. The plasma samples obtained by centrifugation for 10 min at 1000×g were stored at -20°C and completely dissolved before use. The assay of cytokine/chemokine measurement was directed by the manufacturer's instructions of Human 38-plex magnetic cytokine/chemokine kits (EMD Millipore, HCYTMAG-60K-PX38). Fluorescence was quantified using a Luminex 200 instrument, and the concentrations were calculated by Milliplex Analyst software version 4.2 (EMD Millipore). All samples were examined in triplicate.
RESULTS
Clinical outcomes posttransplantation
During the study period, 38 IFLT recipients and 130 CLT recipients were recruited. The detailed clinical data are described in our recently published paper.16 There was no significant difference in donor and recipient characteristics between the two groups. IFLT recipients had a lower incidence of early allograft dysfunction, and higher one-year graft/patient rates than CLT recipients.
Posttransplant liver function tests results
Patients undergoing IFLT had lower peak AST levels (539.59 ± 661.76 U/L vs. 2622.28 ± 3291.57 U/L, p < 0.001) and ALT levels (297.64 ± 549.50 U/L vs. 1184.16 ± 1502.76 U/L, p < 0.001) than those undergoing CLT within the first 7 days posttransplantation (Figure 2A, B). IFLT recipients had lower TBIL levels (3.27 ± 2.82 mg/dl vs. 8.33 ± 8.76 mg/dl, p < 0.001) by day 7 than CLT recipients (Figure 2C).
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Metabolomics profiles of IFLT versus CLT grafts
During the transplant procedure, the IFLT grafts were under continuous normothermic and oxygenated perfusion. In contrast, CLT grafts were under static hypothermic and hypoxic conditions. Therefore, the metabolic activities were substantially different between the two groups, which might impact the pathogenesis of graft IRI. Therefore, the relative abundances of metabolites in the liver biopsies were measured using an LC-MS/MS-based nontargeted metabolomics method. It was difficult to distinguish the liver biopsy samples collected at EP from those collected PR by using both PCA and OPLS-DA models in the IFLT group (p = 0.067). However, the metabolomics profiles could easily distinguish samples collected at EP and PR in the CLT group (p = 0.028) (Figure 3A).
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A volcano plot showed that among the 780 detected (146 annotated and 634 unannotated) metabolites in these samples, there were 146 differentially expressed metabolites (DEMs) (67 lower and 79 higher, VIP > 1, p < 0.05) between the CLT_PR and CLT_EP samples, while among the 587 detected (84 annotated and 503 unannotated) metabolites in these samples, there were 84 DEMs (42 lower and 42 higher, VIP > 1, p < 0.05) in IFLT_PR samples compared to IFLT_EP samples (Figure 3B, Tables S2 and S3). The abundances of a number of amino acids and derivatives (three lower, 14 higher), nucleosides, nucleotides and derivatives (18 lower, six higher), and organic acid (six lower, 17 higher) metabolites were significantly different between CLT_PR and CLT_EP samples (Table S4). Among the 41 metabolic pathways with at least two metabolites captured, 28 were higher (differential abundance score ≥ 0.5, red), and one was lower (differential abundance score ≤ -0.5, blue) in IFLT_EP samples than in CLT_EP samples (Figure 3C, left). Similarly, among the 27 metabolic pathways, 13 were higher, and two were lower in IFLT_PR samples than in CLT_PR samples (Figure 3C, right). Interestingly, most of the upregulated pathways in IFLT_EP relative to CLT_EP were related to amino acid, lipid, and carbohydrate metabolism, whereas the downregulated pathway was related to cofactors and vitamins metabolism. Most of the upregulated pathways in IFLT_PR relative to CLT_PR were related to nucleotide, cofactors and vitamins, energy, and carbohydrate metabolism, whereas the downregulated pathways were related to cofactors and vitamins, and lipid metabolism. Collectively, these results showed a clear metabolic reprogramming from catabolism during preservation to biosynthesis PR during CLT. In contrast, this reprogramming was not obvious during IFLT.
The enrichment analysis and topological analysis showed that the top one differential pathway between IFLT_EP and CLT_EP was the pentose phosphate pathway (PPP) (Figure 3D, left). The top one differential pathway between IFLT_PR and CLT_PR was also PPP (Figure 3D, right). We therefore constructed a metabolic map of the PPP. Gluconolactone and 2-dehydro-3-deoxy-D-gluconate decreased in abundance, while glyceric acid and 2-keto-3-deoxy-6-phosphogluconic acid increased in IFLT_EP samples compared to CLT_EP samples. Both deoxyribose 5-phosphate and deoxyribose were significantly increased in IFLT_EP samples compared to CLT_EP samples, suggesting more active biosynthesis during IFLT_EP than CLT_EP (Figure 4A). Nine DEMs in this pathway were identified when comparing IFLT_EP grafts to CLT_EP grafts. None of these metabolites changed significantly from EP to PR in IFLT grafts. In contrast, the levels of all these metabolites except D-ribulose 5-phosphate, D-ribose, and β-D-fructose 6-phosphate changed significantly from EP to PR in CLT grafts. Overall, the antioxidant PPP was stable throughout IFLT, while this pathway was suppressed during preservation but overactivated PR in CLT (Figure 4B).
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IRI-associated pathological characteristics of IFLT versus CLT grafts
In the PPP, the oxidized form of nicotinamide adenine dinucleotide phosphate (NADP+) is converted to nicotinamide adenine dinucleotide phosphate (NADPH). NADPH is an important reducing equivalent to replenish the reduced glutathione (GSH) pool and maintain redox homeostasis in cells.17 We documented stable levels of the antioxidants GSH and SOD and the oxidant MDA in liver biopsies during IFLT (Figure 5A-C). In contrast, the MDA level was increased, while GSH and SOD levels were decreased in the CLT group. These results suggest that IFLT can maintain redox homeostasis in the grafts through the PPP.
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We then assessed the histological characteristics of IRI in the liver biopsies obtained during the procedures. The Suzuki score was stable during IFLT. In contrast, a significantly increased Suzuki score was observed during CLT (Figure 5D, E). An obvious increase in the number of apoptotic hepatocytes was observed during CLT, whereas the number of apoptotic hepatocytes was stably low during IFLT (Figure 5F, G). Sinusoidal endothelial cell (SEC) activation, as shown by vWF staining, was not obvious in the IFLT group (Figure 5H, I). IFLT grafts showed almost normal ultrastructural appearances. In contrast, CLT grafts exhibited denatured nuclei, damaged mitochondria, damaged rough endoplasmic reticula, and damaged columnar epithelial cells in the common bile duct with microvillus shedding (Figure 5J-L). Thus, the well-known pathological characteristics of IRI were largely reduced in IFLT grafts.
IFLT prevents transcriptional reprogramming and the activation of sterile inflammation
Sharp metabolic changes can induce profound transcriptional reprogramming during liver transplantation.3 Transcriptome analysis of the liver biopsies showed 805 significantly upregulated genes and 58 downregulated genes in the CLT grafts. Strikingly, there were only 11 upregulated genes and 11 downregulated genes in the IFLT grafts (Figure 6A). The expression of the top five DEGs with the smallest p values in the IFLT and CLT groups was verified by RT-qPCR (Figure S1 and Table S5). These data suggest that the IFLT procedure does not trigger transcriptional reprogramming.
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IRI often causes profound sterile inflammation in reperfused grafts.18 KEGG pathway analysis revealed that among the top 10 pathways with significant DEG enrichment, five inflammatory pathways, including “cytokine-cytokine receptor interaction,” “mitogen-activated protein kinase (MAPK) signaling pathway,” “tumor necrosis factor (TNF) signaling pathway,” “IL-17 signaling pathway,” and “nuclear factor kappa B (NF-κB) signaling pathway,” were identified in the CLT group (Figure 6B). There were 59 DEGs enriched in the “cytokine-cytokine receptor interaction” pathway, which was also the top one distinct pathway in the liver biopsies obtained PR between the CLT and IFLT grafts (Figure S2). Of the proinflammatory cytokines associated with graft IRI, TNF-α, IL-1β, and IL-6 are among the most important.1 The transcription of these cytokines was not increased in the IFLT group, while significant increases in the transcription of these cytokines were observed in the CLT group (Figure 6C). The maturation of IL-1β is tightly controlled by the inflammasome complex, which leads to activation of the IL-1β-converting enzyme caspase-1. Activated Caspase-1 then cleaves gasdermin D (GSDMD) to form membrane pores to release proinflammatory IL-1β and IL-18.19 We found significant release of IL-1β and IL-18 (Figure 6D), activation of the inflammasome sensors NOD-like receptor protein-3 (NLRP3) and Caspase-1, and cleavage of GSDMD (Figure 6E) in liver biopsies obtained PR in the CLT group. In contrast, activation of the inflammasome complex and pyroptosis were almost absent in the IFLT group. In addition, studies have shown that the MAPK, Akt and NF-κB pathways are key players in IRI.20,21 We validated that these proinflammatory pathways were hardly activated by phosphorylation in the IFLT grafts as they were in the CLT grafts (Figure 6F).
Proteomics analysis reveals distinct metabolic and immunological characteristics between IFLT and CLT
To further confirm the transcriptome profiling results, proteomics analysis was conducted. A total of 1085 proteins were significantly upregulated, and 917 proteins were downregulated in the CLT group. In contrast, there were only 154 upregulated proteins and 118 downregulated proteins in the IFLT group (Figure 7A). A hierarchical clustering heat map of all identified proteins in the four groups showed significant differences between CLT_PR and CLT_EP samples (Figure 7B). Using quantitative values from proteomics data, PCA and OPLS-DA also indicated more differences in the CLT versus IFLT group (Figure S3). According to the Z-scores of different protein classes, enzymes were the most important differentially expressed proteins (DEPs) between the IFLT and CLT groups (Figure 7C, D). Functional enrichment analysis of the DEPs using Metascape showed that “metabolism of RNA” was the major differentially expressed process between IFLT_EP and CLT_EP samples (Figure 7E), and “regulated exocytosis” and “humoral immune response” were among the major differentially expressed processes between IFLT_PR and CLT_PR samples (Figure 7F). Combined analysis of DEGs and DEPs using MetaCore showed that four of the top 10 Gene Ontology (GO) processes between IFLT_EP and CLT_EP samples were metabolic processes, while “regulated exocytosis” and “neutrophil-mediated immunity” were also among the major differentially expressed processes between IFLT_PR and CLT_PR samples (Figure S4A), which was consistent with the functional enrichment analysis of DEPs.
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Combined analysis of transcriptomics, proteomics, and metabolomics using MetaCore
Combined analysis of DEGs, DEPs, and DEMs in the IFLT_EP and CLT_EP groups by MetaCore showed that the top 10 metabolic networks mainly included amino acid (alanine, glycine, cysteine, glutamic acid, serine, methionine, ornithine, etc.) and lipid (glycosphingolipid and triacylglycerol) metabolism (Figure S4B,C). Among these pathways, the top one was glycine and L-serine metabolism.
Particularly, in line with the metabolomics results, gene transcription and protein expression in the “PPPs and transport” metabolic network were stable throughout IFLT. In contrast, a number of these genes were downregulated during preservation and upregulated PR in the CLT group (Figure 8A). A hierarchical clustering heat map of 25 DEPs between the four groups in the network is shown in Figure 8B.
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The “PPPs and transport” metabolic network identified by the combined analysis of transcriptome, proteomics, and metabolomics data using MetaCore is shown in Figure 8C. There were eight genes and their encoded proteins differentially expressed in the IFLT_EP versus CLT_EP group. Expression of the genes glucose transporter type 9 (GLUT9), nuclear factor I C (NFIC), phosphoglucomutase 1 (PGM1), and catenin beta 1 (CTNNB1) and their encoded proteins were upregulated. The expression of hexokinase 3 (HXK3) and 6-phosphogluconolactonase (6PGL) was downregulated at gene transcription level but upregulated at protein expression level. The expression of glycogen synthase kinase 3 beta (GSK3B) and ribokinase (RBSK) was upregulated at gene transcription level but downregulated at protein expression level.
Glucose transporter type 3 (GLUT3) and GLUT9 transport extracellular D-glucose into cells. PGMU catalyzes the biotransformation of alpha-D-ribose-1-phosphate to D-ribose 5-phosphate. RBKS catalyzes the biotransformation of adenosine triphosphate (ATP) and D-ribose to D-ribose 5-phosphate and adenosine diphosphate (ADP). These key players of the PPP, including GLUT9, PGMU, D-ribose, and D-ribose 5-phosphate, were all upregulated in the IFLT_EP versus CLT_EP group.
Local immunity and systemic inflammation were suppressed in IFLT grafts
Sterile inflammation subsequently recruits and activates innate and acquired immune cells during IRI.3 The transcription levels of the chemokines C-X-C motif ligand-1 (CXCL1), CXCL2, and CXCL3 were upregulated in the CLT group (Figure 9A). In contrast, the transcription levels of these chemokines were stable in the IFLT group. The number of T cells was comparable between the two groups (Figure 9B). The number of natural killer (NK) cells in the grafts PR was lower in the IFLT versus CLT group (Figure 9C). A more obvious increase in neutrophils PR was documented in the CLT group when compared to the IFLT group (Figure 9D). Unexpectedly, the number of macrophages increased PR in the IFLT grafts instead of the CLT grafts (Figure 9E).
Transcriptome analysis showed that expression of a number of genes involved in T cell activation, macrophage activation, NK cell-mediated immunity, and neutrophil-mediated immunity was enhanced after PR in the CLT group in comparison to the IFLT group (). Furthermore, significantly higher levels of 14 cytokines, including IL-1, IL-1RA, IL-2, IL-8, IL-10, IL-15, IL-17A, TNF-α, interferon (IFN)-γ, interferon-inducible protein (IP)-10, monocyte chemoattractant protein (MCP)-1, and granulocyte-macrophage colony stimulating factor (GM-CSF), were found in the serum of recipients on day 1 posttransplantation in the CLT versus IFLT group (Figure 9F). Collectively, these results suggest a largely suppressed local and systemic inflammation in IFLT.
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DISCUSSION
During conventional transplant procedures in all types of solid organ transplantation, oxygenated blood supply is completely interrupted throughout organ procurement, ex situ preservation, and implantation. After revascularization, the graft can definitely suffer subsequent IRI. However, the pathophysiological complexity of this event remains only poorly understood and is complicated by the concurrence of the allograft rejection response.1 Our IFLT approach is an entirely novel approach with no graft ischemia, providing unique clinical and research opportunities for investigating the mechanisms of IRI. In the current study, we examined the pathological, transcriptome, proteome, metabolome, and immunological profiles of IFLT and CLT grafts to provide a landscape on how IFLT might impact graft IRI.
A key pathological characteristic of graft IRI is the presence of many kinds of cell death, including necrosis, apoptosis, and pyroptosis.22–24 The Suzuki score based on HE staining and apoptosis analysis of liver graft biopsies suggested an almost complete absence of necrosis and apoptosis in IFLT grafts. In addition, inflammasome-mediated pyroptosis was also largely reduced. Moreover, the TEM results also revealed optimal preservation of the ultrastructure of the grafts in the IFLT group. Collectively, these comprehensive pathological data show for the first time that, by using IFLT, graft IRI can be largely avoided. However, the AST/ALT levels were still increased post-IFLT. Our previous study showed that liver enzyme levels were slightly increased during ex situ NMP,25 suggesting that NMP technology itself might also induce graft injury, although a continuous blood supply can be maintained during the procedure. Recently, we documented normal AST/ALT levels on day 1 post-IFLT in one patient. Therefore, further modifying this procedure might eventually result in a complete avoidance of graft IRI.
During CLT, grafts were subjected to hypothermic and anaerobic metabolism due to the interruption of the blood supply. In sharp contrast, the grafts maintained normothermic and aerobic metabolism throughout IFLT. The metabolomics analysis showed that the metabolic activities of amino acids, lipids, and carbohydrates were suppressed in CLT grafts compared with IFLT grafts. The suppressed functions of a large number of metabolic enzymes identified by the proteomics analysis (Tables S6, S7) might explain the distinct metabolomics profiles. Importantly, we found that the most pronounced metabolic pathway distinguishing CLT from IFLT grafts in both the EP and PR stages was the PPP. Reactive oxygen species (ROS) are the key players in liver IRI, leading to cell death and ultrastructural damage.1 ROS detoxification requires the maintenance of GSH by NADPH generated by the PPP. Studies have shown that its rate-limiting enzyme, glucose-6-phosphate dehydrogenase (G6PDH), can protect the brain and heart from IRI.26,27 Furthermore, the PPP is the key to maintaining mitochondrial function.28 Impaired mitochondrial function plays an essential role in allograft IRI.29 In this study, transcriptome, proteome, and metabolome network analysis confirmed that PPP activity was stable throughout IFLT, while it was suppressed during preservation but enhanced postrevascularization in CLT. Consistently, ROS production was enhanced, and the antioxidants GSH and SOD were diminished PR in CLT grafts, while redox hemostasis was maintained in IFLT grafts. These results indicate that IFLT might prevent oxidative stress in grafts by maintaining stable antioxidative PPP activity. However, it is still unknown how IFLT might affect mitochondrial function.
To adapt to anaerobic metabolism, significant transcriptional reprogramming occurs during liver transplantation.3 In the current study, transcriptome analysis confirmed this phenomenon in the CLT group, while it was largely prevented in the IFLT group. Importantly, transcriptome analysis showed that several inflammatory pathways, including the NF-κB, MAPK, TNF-α, and IL-17 pathways, with large numbers of DEGs were activated in the CLT group and were almost inactivated in the IFLT group. These results were further confirmed by RT-qPCR, Western blotting and ELISA. It has been reported that these pathways are key mediators and potential therapeutic targets of graft IRI.30–32 However, it is almost impossible to simultaneously target all of these pathways by either pharmacological methods or gene therapy. In addition, intragraft sterile inflammation is a well-known characteristic that shapes the long-term immune microenvironment during IRI.33 Studies have shown that sterile inflammation is associated with chronic graft loss.34 Therefore, IFLT might provide benefits for long-term graft survival.
Importantly, sterile inflammation during IRI may not only damage the graft itself but also initiate the recruitment of innate and adaptive immune cells, leading to augmented alloimmunity and more frequent rejection.35 It is well known that neutrophils, macrophages and NK cells all play critical roles in the pathogenesis of graft IRI.36–38 We showed decreased levels of chemokines by RT-qPCR and reduced numbers of NK cells and neutrophils by immunohistochemical staining, as well as reduced activity of NK cells, macrophages and neutrophils by transcriptome analysis, in IFLT grafts compared to CLT grafts. Proteome analysis also showed that neutrophil-mediated immunity was enhanced in CLT grafts compared to IFLT grafts. However, we did not find a significantly reduced incidence of allograft rejection in the IFLT group,16 probably due to the use of powerful immunosuppressive drugs and the limited sample size. Rebecca et al reported that exposure of the liver to IRI may subsequently cause inflammatory responses in other organs, which might lead to multiorgan failure.39 Indeed, we documented significant decreases in 14 cytokines in the recipients’ serum on day 1 posttransplantation in the IFLT versus CLT group. Considering the profound differences in intragraft immunity and systemic inflammation early posttransplantation, it will be of great importance to investigate how IFLT alters the incidence and characteristics of allograft rejection in an animal model.
There are some weaknesses in the current study. First, due to the limited samples collected, we could not conduct all the analyses in all the patients included in the clinical trial, which might lead to sample selection bias. Second, this study aimed to outline the comprehensive impacts of IFLT on the pathogenesis of IRI. Future studies should focus on specific mechanisms. Finally, all the findings were from human samples, and the gain or loss of function experiments in animal studies is pending.
In conclusion, these results show that IFLT is an efficient approach to minimize IRI, which might improve transplant outcomes and increase the availability of organs for transplantation. In addition, this novel approach provides a unique model for investigating the molecular mechanism of graft IRI and elucidating the interaction between IRI and allograft rejection.
ACKNOWLEDGMENTS
We would like to thank all members of the organ procurement organization, surgical intensive care unit, transplant anesthesia team, and cardiopulmonary bypass team, as well as all the donors and patients. This work was supported by the National Natural Science Foundation of China (grant number: 82070670 to Xiaoshun He and grant number: 81970564 to Zhiyong Guo), the Guangdong Provincial Key Laboratory Construction Projection on Organ Donation and Transplant Immunology (grant numbers: 2013A061401007 and 2017B030314018 to Xiaoshun He), the Guangdong Provincial International Cooperation Base of Science and Technology (Organ Transplantation) (grant number: 2015B050501002 to Xiaoshun He), the Science and Technology Program of Guangzhou (grant number: 201704020150 to Xiaoshun He), the Science and Technology Program of Guangdong (grant number: 2020B1111140003 to Xiaoshun He), the Sun Yat-sen University Young Teacher Key Cultivate Project (grant number: 19ykzd13 to Zhiyong Guo), and the “Elite program” that is specially supported by the China Organ Transplantation Development Foundation (to Zhiyong Guo).
ETHICS APPROVAL AND CONSENT TO PARTICIPATE
The study protocol (ChiCTR-OPN-17012090) was carried out in compliance with institutional and governmental requirements approved by the Ethics Committee of the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
DATA AVAILABILITY STATEMENT
All data associated with this study are presented in the paper or the Supplementary Materials. The GEO accession number for the microarray data reported in this paper is GEO: GSE113024.
CONFLICT OF INTEREST
The authors declare that they have no competing interests.
AUTHOR CONTRIBUTIONS
Xiaoshun He,Zhiyong Guo, Jinghong Xu, Shanzhou Huang, and Meixian Yin contributed to the conceptualization and trial design. Zhiyong Guo, Jinghong Xu, Shanzhou Huang, Meixian Yin, Kunpeng Liu, Yuting Lu, and Haitian Chen managed the samples and performed relevant experiments. Qiang Zhao, Weiqiang Ju, Dongping Wang, Ningxin Gao, Changjun Huang, Lu Yang, Maogen Chen, Linhe Wang, Caihui Zhu, Yixi Zhang, Yunhua Tang, and Zhiheng Zhang. contributed to data collection. Xiaoshun He, Zhiyong Guo, Jinghong Xu, Shanzhou Huang, Meixian Yin, Yi Ma, Anbin Hu, Yinghua Chen, and Xiaofeng Zhu analyzed and interpreted the data. Zhiyong Guo, Jinghong Xu, Shanzhou Huang, and Meixian Yin drafted the manuscript, which was critically reviewed and revised by Xiaoshun He, Zhiyong Guo, Anbin Hu, Yinghua Chen and Xiaofeng Zhu. Zhiyong Guo, Jinghong Xu, Shanzhou Huang, and Meixian Yin contributed equally to the work and should be considered first coauthors. All authors reviewed and approved the final manuscript.
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Abstract
Background
Ischemia-reperfusion injury (IRI) is considered an inherent component of organ transplantation that compromises transplant outcomes and organ availability. The ischemia-free liver transplantation (IFLT) procedure has been developed to avoid interruption of blood supply to liver grafts. It is unknown how IFLT might change the characteristics of graft IRI.
Methods
Serum and liver biopsy samples were collected from IFLT and conventional liver transplantation (CLT) recipients. Pathological, metabolomics, transcriptomics, and proteomics analyses were performed to identify the characteristic changes in graft IRI in IFLT.
Results
Peak aspartate aminotransferase (539.59 ± 661.76 U/L versus 2622.28 ± 3291.57 U/L) and alanine aminotransferase (297.64 ± 549.50 U/L versus 1184.16 ± 1502.76 U/L) levels within the first 7 days and total bilirubin levels by day 7 (3.27 ± 2.82 mg/dl versus 8.33 ± 8.76 mg/dl) were lower in the IFLT versus CLT group (all p values < 0.001). The pathological characteristics of IRI were more obvious in CLT grafts. The antioxidant pentose phosphate pathway remained active throughout the procedure in IFLT grafts and was suppressed during preservation and overactivated postrevascularization in CLT grafts. Gene transcriptional reprogramming was almost absent during IFLT but was profound during CLT. Proteomics analysis showed that “metabolism of RNA” was the major differentially expressed process between the two groups. Several proinflammatory pathways were not activated post-IFLT as they were post-CLT. The activities of natural killer cells, macrophages, and neutrophils were lower in IFLT grafts than in CLT grafts. The serum levels of 14 cytokines were increased in CLT versus IFLT recipients.
Conclusions
IFLT can largely avoid the biological consequences of graft IRI, thus has the potential to improve transplant outcome while increasing organ utilization.
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Details
; Xu, Jinghong 1
; Huang, Shanzhou 1 ; Yin, Meixian 1 ; Zhao, Qiang 1 ; Ju, Weiqiang 1 ; Wang, Dongping 1 ; Gao, Ningxin 1 ; Huang, Changjun 1 ; Lu, Yang 2 ; Chen, Maogen 1 ; Zhang, Zhiheng 1 ; Zhu, Zebin 1 ; Wang, Linhe 1 ; Zhu, Caihui 1 ; Zhang, Yixi 1 ; Tang, Yunhua 1 ; Chen, Haitian 1 ; Liu, Kunpeng 1 ; Lu, Yuting 1 ; Ma, Yi 1 ; Hu, Anbin 1 ; Chen, Yinghua 1 ; Zhu, Xiaofeng 1 ; He, Xiaoshun 1 1 Organ Transplant Centre, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China; Guangdong Provincial Key Laboratory of Organ Donation and Transplant Immunology, Guangzhou, China; Guangdong Provincial International Cooperation Base of Science and Technology (Organ Transplantation), Guangzhou, China
2 Department of Anaesthesiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China