Ephrin-B2/Fc promotes proliferation and migration, and suppresses apoptosis in human umbilical vein endothelial cells

Tumor growth and metastasis are angiogenesis dependent. Angiogenic growth involves endothelial cell proliferation, migration, and invasion. Ephrin-B2 is a ligand for Eph receptor tyrosine kinases and is an important mediator in vascular endothelial growth factor-mediated angiogenesis. However, research offer controversial information regarding effects of ephrin-B2 on vascular endothelial cells. In this paper, proteome analyses showed that ephrin-B2/Fc significantly activates multiple signaling pathways related to cell proliferation, survival, and migration and suppresses apoptosis and cell death. Cytological experiments further confirm that ephrin-B2/Fc stimulates endothelial cell proliferation, triggers dose-dependent migration, and suppresses cell apoptosis. Results demonstrate that soluble dose-dependent ephrinB2 can promote proliferation and migration and inhibit apoptosis of human umbilical vein endothelial cells. These results also suggest that ephrinB2 prevents ischemic disease and can potentially be a new therapeutic target for treating angiogenesis-related diseases and tumors.


INTRODUCTION
Tumor growth and metastasis are angiogenesis dependent. Blood vessels support cancer cells with nutrients and allow communication between primary and metastatic tumors [1][2][3]. Anti-angiogenesis is an efficient antitumor strategy for its protective effects against tumor emergence and progression [4][5][6]. Tyrosine protein kinase family includes ephrin and its receptor Eph as leading members and is considered as key factor for angiogenesis and lymphatic valve development [7,8]. As one of the key genes in angiogenesis [9], ephrin-B2 is very important in regulating embryonic and adult angiogenesis and tumor angiogenesis [10][11][12].
Migration and proliferation of endothelial cells are prerequisites of solid tumor angiogenesis. However, research offer controversial information regarding effects of ephrin-B2 on vascular endothelial cells. Some studies showed that ephrin-B2 promotes migration and proliferation of endothelial cells [25][26][27]. On the other hand, other studies drew different conclusions [16,28]. Systematic research is still needed to further clarify mechanisms of ephrin-B2 and its effects on endothelial cells.
In the present study, by using quantitative global and phosphorylated proteomics technological methods associated with bioinformatics analysis, we systematically and comprehensively revealed effects of ephrin-B2 on cellular functions and signaling pathways of human umbilical vein endothelial cells (HUVECs). Results showed that ephrin-B2 promoted proliferation, survival, migration, cell cycle, and suppressed apoptosis of HUVECs. Similar results were observed in further cellular experiments. These data suggest that ephrinB2 plays a protective role in ischemic disease and can potentially be a new therapeutic target for treating angiogenesis-related diseases and tumors.

Identification and quantification of differentially expressed proteins induced by ephrin-B2 treatment
To study the effect of ephrin-B2 on HUVECs, we isolated and identified primary HUVECs from freshly isolated umbilical cords. Immunohistochemical results demonstrated positive expression of factor-VIII-related antigen in isolated cells (Supplementary Figure 1); this positive expression proved successful isolation of HUVECs. HUVECs were cultured in stable isotope labeling by amino acids in cell culture (SILAC) media and treated with ephrin-B2/Fc or phosphate-buffered saline (PBS) for 15 h. Global and phosphorylated proteins were then prepared and subjected to liquid chromatography tandem-mass spectrometry analysis. Among 1720 global proteins identified, 258 were differentially expressed; 134 proteins increased, whereas 124 proteins decreased. For phosphorylated proteins, 395 differentially expressed proteins were identified from 1377 phosphorylated sites. According to phosphorylation level, 354 proteins were upregulated, whereas 41 proteins were down-regulated.

Functional analyses: Ephrin-B2 promoted proliferation and migration and suppressed apoptosis in HUVECs
To functionally characterize differentially expressed proteins, we used Ingenuity Pathway Analysis (IPA) to associate these proteins to certain molecular and cellular functions in the Ingenuity Knowledge Base database. pvalue was calculated using right-tailed Fisher's exact test to assess association level. Functions were arranged per -log(p-value). As shown in Figure 1A, for differentially expressed global proteins, the top five molecular and cellular functions were post-translational modification, protein folding, cell death and survival, cell-to-cell signaling and interaction, and cellular assembly and organization. For differentially expressed phosphorylated proteins, the top five molecular and cellular functions were gene expression, cellular growth and proliferation, cellular assembly and organization, cellular function and maintenance, and cell death and survival ( Figure  1B). Among these functions, cell death and survival (labeled with dotted box) exhibited relatively high association levels and differential molecules in both global and phosphorylated proteins. Cellular growth and proliferation presented the highest number of differential molecules (215) in phosphorylated proteins. Z-scores were calculated according to expression level (up or down) of corresponding molecules in experiments and expected expression values (up or down) in pathways or functions. Z-scores ≥ 2 (≤ -2) indicate that function or signaling pathway is statistically and significantly activated (inhibited). As listed in the tables (Tables 1 and  2 and Supplementary Tables 3 and 4), with high absolute values of z-scores (|z-score| ≥ 2), ephrin-B2 suppressed cell apoptosis (z = -3.563/-2.329) and death (z = -3.5373/ -2.938) and promoted cell survival (z = 2.8823/3.825), proliferation (z = 2.425/3.818), movement (z = 4.2183/3.118), and migration (z = 3.9823/3.194). Ephrin-B2 also promoted angiogenesis (z = 2.928) in phosphorylated proteins (Supplementary Table 4).

Signal pathway analyses: Ephrin-B2 activated signaling pathways involved in cell growth, proliferation, and movement
Among signaling pathways involving differentially expressed global proteins, endothelial nitric oxide synthase (eNOS) signaling showed the highest association level and z-score (2.236), indicating activation of this (B) Molecular and cellular functions involving differentially expressed phosphorylated proteins. p-value was calculated using right-tailed Fisher's exact test to assess association level. Functions were arranged according to -log(p-value). Threshold line indicating significant level was set at p = 0.05, or -log(p-value) = 1.3 means. The number on top of bar represents differentially expressed proteins involved in specific molecular pathways. Note: "Function annotation" includes biological functions involving differentially expressed proteins. p-value represents matching contingency of data, and corresponding function, |z-score| ≥ 2 is considered as prediction index of downstream effect.  Figure 2, Table 3, and Supplementary Table  5). Rho GTPases showed the highest association level among signaling pathways involving differentially expressed phosphorylated proteins. Many important signaling pathways showed significant association and were activated in phosphorylated proteins ( Figure 3, Table 4, and Supplementary Table 6). These signaling pathways include integrin signaling, GΑ12/13 signaling, telomerase signaling, ERK5 signaling, insulin-like growth factor 1 (IGF-1) signaling, Rac signaling, ERK/mitogenactivated protein kinase (MAPK) signaling, VEGF signaling, hepatocyte growth factor (HGF) signaling, and with differentially expressed global proteins, eNOS signaling exhibited the highest correlation and z-score (2.236), indicating pathway activation. p-value was calculated using right-tailed Fisher's exact test to assess association level. p < 0.05 or -log(p-value) > 1.3 (the main axis or bar chart) signifies significant association. Threshold line indicating significant level was set at p = 0.05 or -log(p-value) = 1.3 means. Z-score is calculated according to expression level (up or down) of corresponding molecules in experiments and expected expression value (up or down) in pathways. Z-scores ≥ 2 or ≤ -2 indicate that signaling pathway was statistically and significantly activated (colored in yellow) or inhibited (colored in blue). The ratio denotes proportion of differentially expressed genes in total signaling pathway genes; such ratio is provided as reference for significance assessment.

Interaction network analyses indicated that ephrin-B2 participated in multiple cellular functions
To characterize the effects of ephrin-B2 on HUVECs by functional protein groups, identified differentially expressed proteins, called focus genes in IPA, were used as starting point to generate biological networks defined by the Ingenuity Knowledge Base database. Out of 258 differentially expressed global proteins, 79 were mapped to four highly significant networks (score ≥ 10, Supplementary Table 1 Figure 2), whereas out of 395 differentially expressed phosphorylated proteins, 131 were mapped to six highly significant networks (score ≥ 10, Supplementary Table 2 Figure 3). Networks were scored for likelihood of finding focus gene(s) in a given network. Biological relationship between two nodes was represented as an edge (line). Node color intensity indicated up-regulation (red) or down-regulation (green) degree. These networks demonstrated functional protein groups that are associated with multiple functions, such as cell death and survival, cellular assembly and organization, cellular growth and proliferation, cell cycle, cell morphology, and cellular movement, suggesting that ephrin-B2 is involved in multiple cellular functions.

Results of in vitro cytological experiments
Proteomic analysis indicated that ephrin-B2 promoted HUVECs proliferation, survival, migration, and cell cycle. To verify these effects, cytological experiments were performed in vitro.

Ephrin-B2 promoted HUVECs proliferation
Cell Counting Kit-8 (CCK-8) assay showed that ephrin-B2 significantly promoted endothelial cell proliferation at concentration of 0.3 or 1 μg/mL ( Figure   4A). Higher concentration allows faster cell growth, suggesting that ephrin-B2 enhanced HUVEC proliferation in dose-dependent manner. Cell cycle detection showed that G0/G1 phase cell ratio was significantly reduced after ephrin-B2 treatment, whereas S phase cell proportion was elevated ( Figure 4B). Western blot results further indicated that expression levels of c-Myc and nucleophosmin (NPM), which promote cell proliferation, increased after ephrin-B2 treatment ( Figure 4C and 4D).

Ephrin-B2 promoted HUVECs migration
Angiogenesis is mainly involved in endothelial cell migration and proliferation. Proteomic analysis indicated that ephrin-B2 can promote endothelial cell movement and migration. Wound healing experiment and Transwell assay were performed to confirm above results. Wound healing experiments showed that migration distance increased with ephrin-B2 concentration compared with that of the control group ( Figure 5A). This result indicated dose-dependent enhancement of the effect of ephrin-B2 on HUVEC migration. Transwell experiment showed that ephrin-B2 promoted endothelial cell migration at concentrations from 0.1 μg/mL to 1 μg/mL and enhanced effect peaked at 1 μg/mL. However, number of migrated cells treated with 3 μg/mL ephrin-B2 did not significantly change compared with that of the control group ( Figure  5B). This result indicated that the effect of ephrin-B2 on endothelial cell migration was dose-dependent at 0-1 μg/ mL, and that enhanced effect disappeared when ephrin-B2 concentration reached 3 μg/mL. Western blot results further indicated that pro-migration protein Twist and matrix metallopeptidase 9 (MMP9) expression increased after treatment with 1 μg/mL ephrin-B2. Twist expression increased immediately to a high level (5 min) and then declined, whereas no significant increase was observed for MMP9 until 2 h after ephrin-B2 incubation ( Figure 5C and 5D).

Ephrin-B2 inhibited apoptosis in HUVECs
To detect cell apoptosis protection by ephrin-B2, H 2 O 2 was used as inducer for apoptosis. As shown in Figure 6A, HUVECs survival ratio declined significantly     when H 2 O 2 concentration reached 0.3 mmol/L. After ephrin-B2 treatment for prior protection, survival ratio showed dose-dependent improvement ( Figure 6B). Western blot analysis showed increased level of antiapoptotic protein Bcl-2 expression after ephrin-B2 treatment ( Figure 6C), whereas cleaved caspase 3 gradually decreased by 1 μg/mL ephrin-B2 ( Figure 6D).

Ephrin-B2 activated some HUVEC signaling pathways
As shown in Figure 3, many signaling pathways were activated or inactivated by ephrin-B2. However, verifying all changes was difficult. We attempted to detect the effect of ephrin-B2 on PI3K-Akt, VEGF, and P38 signaling pathways, which have close relationship with cell proliferation, migration, and survival, respectively. As shown in Figure 7A, pAkt (Thr308) expression was increased by ephrin-B2. eNOS is a PI3K-Akt downstream factor; its expression level increased following Akt activation ( Figure 7B). Ephrin-B2 treatment significantly increased pP38 (Thr180/182) level, demonstrating activation of P38 signaling pathway ( Figure 7C).

DISCUSSION
Endothelial cell proliferation and migration are two major events during angiogenesis [29]. Previous studies on Cell survival ratios were then tested at OD450 nm. Relatively significant level of apoptosis was observed at concentration of 0.3 mmol/L (n = 3, mean ± SEM; ns, *p < 0.05, ***p < 0.001 vs. control using ANOVA and Dunnett's multiple comparison test). (B) Different concentrations of ephrin-B2/Fc (0.1, 0.3, and 1 μg/mL) contribute to protecting HUVECs from apoptosis, which is induced by H 2 O 2 (0.3 mmol/L). Cells were cultured in serum-free medium containing different concentrations of ephrin-B2/Fc or PBS for 2 h then incubated with H 2 O 2 for 4 h. Cell survival ratios were also tested on OD450 nm. Cells treated by 1 μg/mL ephrin-B2 showed higher survival ratio (n = 3, mean ± SEM; ns, **p < 0.01 vs. control using ANOVA and Dunnett's multiple comparison test). (C-D) Western blot showed the effects of ephrin-B2 on Bcl-2 and cleaved caspase 3 protein expression levels. Bands were quantified using Quantity One software (mean ± SEM; ns, **p < 0.01, ***p < 0.001 and ****p < 0.0001vs. control using ANOVA and Dunnett's multiple comparison test). the role of ephrin-B2 in endothelial cells mainly focused on cell growth, proliferation, and migration [25,30]. In the present study, proteomic analysis revealed that ephrin-B2 significantly activated multiple signaling pathways related to cell proliferation, survival, and migration and suppressed apoptosis and nuclear factor erythroid 2-related factor 2 (NRF2)-mediated oxidative stress response. Cytological experiments further confirmed that ephrin-B2 stimulated proliferation, caused HUVECs dose-dependent migration, increased anti-apoptotic Bcl-2 expression, proproliferation proteins c-Myc and NPM, and pro-migration proteins Twist and MMP9, activated Akt/eNOS and P38 signaling pathways, and inhibited activation of caspase 3.
Different studies reported contradicting results regarding the effects of ephrin-B2 on endothelial cells. Some evidence indicated that by interfering VEGF and Ang-1 signal transmissions, ephrin-B2 inhibits proliferation, migration, and vascular budding of endothelial cells, where EphB4 receptors are located, thereby inhibiting angiogenesis [28,30,31]. By contrast, other studies showed that ephrin-B2 promotes proliferation and migration by activating EphB4 receptors [25,32,33]. This discrepancy may be explained by different experimental models used or ephrin-B2 concentration variations in those studies. In the current study, as exhibited in our cytological experiments, potency of promoting migration by ephrin-B2 was strong when concentration was set to 0.3 and 1 μg/mL, which are lower than the dosage used in previous studies. Endothelial progenitor cells were treated with 3 μg/ml Eph-B2-Fc in Foubert's  eNOS (B), and pP38 (C) were detected by Western blot. Intensity of each band was quantified by Quantity One software (mean ± SEM; ns, **p < 0. 01 and ***p < 0.001, ****p < 0.0001, vs. control using ANOVA and Dunnett's multiple comparison test). β-actin was used as internal control. study [34]. In Mansson-Broberg's study [35], 0.5, 5, and 10 μg/mL Eph-B2 were used in human adult endothelial cell cultures, and a single dose of 20 μg ephrinB2-Fc was used for C57BL/6 mice weighing 25 g. However, enhancement of migration by 3 μg/mL ephrin-B2 was not significant in the current study. Ephrin-B2 from different sources may possess different activity, possibly resulting in significant differences in effective concentration of ephrin-B2. However, variable results in previous reports and our study most possibly reflect the dependence of ephrin-B2 effects on experimental models or ephrin-B2 concentration used.
Previous studies explored specific signaling pathways to explain the effects of ephrin-B2 on cells. Such research is often segmentary, and results may not reflect all changes induced by ephrin-B2. By quantitatively analyzing alteration in global and phosphorylated protein expression profiles of HUVECs, the current study systematically and comprehensively uncovered cellular function changes and associated signaling pathways mediated by ephrin-B2. Previous studies on ephrin-B2 did not report alterations in these signaling pathways or their cellular functions. These alterations can provide clues to future research on ephrin-B2 mechanism. For example, inactivated signaling pathways including NRF2-mediated oxidative stress response, peroxisome proliferator activated-receptor (PPAR) signaling, and PPARα/retinoid X receptor α (RXRα) activation, were all related to oxidative stress (blue bar in Figure 2 and 3); though not meeting threshold z-score, these results may be a clue to explain Foubert's finding [34], which indicated that in wound healing, Eph-B2 improves beneficial effects of endothelial progenitor cell in physiological and irradiated conditions only when in association with antioxidant treatment. Mansson-Broberg's study [35] also showed that in hypoxic environment, proliferation rate of human adult endothelial cells is significantly lower in ambient air, and adding ephrin-B2 (0.05, 0.5, 5, and 10 μg/ mL) increases proliferation rate (p < 0.10). These previous studies and ours revealed that inactivated oxidative stress related signaling pathways possibly modulate effects of ephrin-B2. The link between these phenomena is worth further study.
Here, we also observed an alteration on signaling pathway of Fc gamma receptor-mediated phagocytosis in macrophages and monocytes (Figure 2 and Figure 3). Although the z-score indicated by IPA is no of significance (1.342 in Figure 2 and 0.816 in Figure 3), there is still a possibility that part of response we detected may be due to Fc gamma receptor stimulation, since ephrin-B2/Fc was used as the stimulant. However, we do not think Fc gamma receptor cause too much disturbance to our conclusion. Recombinant protein ephrin-B2/Fc has been used by many researchers for studying the function of ephrin-B2 [36][37][38]. In fact, since half-life of Fc recombinant proteins is much longer than their original form, Fc has been widely used to produce Fc fusion proteins in pharmaceutical field [39]. Moreover, the only Fc receptor expressed in endothelial cells is the neonatal Fc receptor (FcRn) [40]. Its main function in endothelial cells is to protect IgG or fusion proteins from being metabolized [41]. Therefore, we think Fc is unlikely to cause any remarkable response in HUVECs.
In the present study, through a series of proteomic and cytological experiments, we proved that ephrin-B2 exerts dose-dependent effects on HUVEC proliferation and migration and suppresses cell apoptosis. Considering its positive roles in promoting endothelial cell proliferation and migration, ephrin-B2 is expected to be a therapeutic candidate in angiogenesis-related diseases and tumor.
As a reversible and transient modification, phosphorylation is mostly studied at the beginning stage of stimulation. In this study, we choose to perform analyzing events on changes of global and phosphorylated proteins at the same stage (15 h after stimulation), to make our conclusions more persuasive. We think that phosphorylation must play a key role in both the initial signal transduction and subsequent signaling pathway and protein function regulation. Phosphorylation is the most ubiquitous post-translational modification (PTM) a protein experiences throughout its lifetime. It serves to modify protein function by altering protein stability, cellular location, substrate affinity, complex formation, and activity [42]. Therefore, not only the expression level of proteins but also the phosphorylation level of related proteins is changed by ephrin-B2 at 15h. In fact, our results demonstrated a large number of phosphorylated proteins were changed at 15h (1377 phosphorylated sites of 395 proteins). And many biofunctions revealed by proteomics analysis of global and phosphorylated proteins were consistent (Table 1 and 2).
Notably, this current study examined only the effects of ephrin-B2 on HUVECs in vitro. Though results of proteomic analysis agree with results of cell-level assays, the present study cannot provide final answers to existing open questions or solve previous controversies. Further experiment in vivo should be carried out to clarify functions and mechanisms of ephrin-B2 on endothelial cell proliferation and migration.

Chemical
Ephrin-B2/Fc was purchased from R&D Systems (USA). All antibodies were purchased from Cell Signaling Technology, Inc. SILAC kits were purchased from Thermo Fisher Scientific, Inc. (USA). Other chemical compounds were purchased from Sigma (USA). www.impactjournals.com/oncotarget

HUVEC isolation and culture
All research involving human subjects were conducted in agreement with the Declaration of Helsinki. Studies involving HUVECs were approved by the Ethical Review Board of the Medical College of Xiamen University, and an informed consent was signed by suppliers. Freshly isolated umbilical cords were obtained from affiliated Zhongshan Hospital of Xiamen University.
Umbilical veins were washed thrice with cold sterile PBS (Gibco). Both ends of umbilical veins were bound and filled with 0.05% trypsin-ethylenediaminetetraacetic acid (EDTA) buffer (Gibco). After incubation for 10 min at 37 °C, endothelial cells were washed with Dulbecco's modified Eagle's medium (DMEM) containing 20% fetal bovine serum (FBS, Gibco) and subsequently centrifuged at 400 × g for 10 min at 4 °C. Separated cells were cultured in DMEM containing 20% FBS, and adherent cells were preserved for passage in accordance with conventional method. In the present study, all cells used were cultured for four to six passages.

SILAC labeling and cell treatment
Isolated HUVECs were cultured in DMEM medium containing 10% FBS at 37 °C with 95% air and 5% CO 2 . Cells were labeled with "heavy" SILAC media (Thermo) containing 0.1 g/L 13 C 6 15 N 2 L-Lysine-2HCl and 0.1 g/L 13 C 6 15 N 4 L-Arginine-HCl or "light" SILAC media (Thermo) containing 0.1 g/L L-Lysine-2HCl and 0.1 g/L L-Arginine-HCl. After five times of passage and 80% confluence, cells labeled with light amino acid were treated with 1 μg/mL ephrin-B2/Fc for 15 h, whereas cells labeled with heavy amino acid were treated with PBS for 15 h.

Peptide preparation
Cells were lysed in urea lysis buffer (8 M urea in 0.1 M Tris-HCl, pH 8.5) containing protease and phosphatase inhibitors. Protein concentration was determined by Bradford assay. Equal amounts (125 μg) of light or heavyisotope-labeled proteins were mixed and precipitated in pre-cooled acetone (-20 °C) for at least 1 h. Depending on different applications, precipitated protein was handled through the following steps:

Differentially expressed global protein sample
Precipitated proteins were dissolved in radioimmunoprecipitation assay (RIPA) lysis buffer and separated by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) after centrifugation at 3,000 × g for 10 min. Gel was equally cut off into nine pieces on the basis of protein molecular weight. Each gel piece was reduced using DL-Dithiothreitol (DTT), alkalized with iodoacetamide (IAM), and in-gel digested with modified trypsin (Promega). Peptides were extracted, desalted with SepPak C18 (Waters, USA), and stored at -80 °C.

Differentially expressed phosphorylated protein sample
After centrifugation at 3,000 × g for 10 min, precipitated proteins were dissolved in 200 μL of urea lysis buffer containing 0.05 M DTT for 45 min and then mixed with 300 μL of iodoacetamide (IAM) solution (0.05 M IAM in urea lysis buffer). Mixture was incubated in the dark for 20 min and centrifuged in an ultrafiltration tube (Millipore, 30 K) at 14,000 × g for 15 min. Up to 300 μL of ammonium bicarbonate (ABC) solution (0.05 M NH 4 HCO 3 in H 2 O) was added into ultrafiltration tube and then subsequently centrifuged at 14,000 × g for 15 min. This step was repeated twice. Trypsin (1:50) was added to protein samples, and resulting mixture was added to 100 μL of ABC solution. The sample was vibrated and incubated at 37 °C for 4-18 h. Up to 50 μL of H 2 O was added, and the tube was centrifuged in a new collector at 4 °C for 15 min. This step was repeated, and liquid effluents containing peptides were combined. Subsequently, 1% formic acid (final concentration) was added to effluents, which were desalted with SepPak C18. Peptides were dried and stored at -20 or -80 °C. Phosphorylated peptide enrichment was performed using titanium dioxide affinity chromatography for phosphorylated protein analysis.

Peptide detection and data analysis
Dried peptides were dissolved in 0.1% formic acid/2% acetonitrile and analyzed on AB Sciex Triple TOF 5600 mass spectrometer (MS) system. Acquired raw data files (.wiff) were searched using Protein Pilot software V.4.2 (AB Sciex, USA) against protein sequence database. Finally, obtained data were uploaded to IPA (https://www. qiagenbioinformatics.com/products/ingenuity-pathwayanalysis/) for bioinformatics analysis. As SILAC is a highly accurate quantitative method, cutoff for fold change was set to 1.50, and p-value was less than 0.05. This study employed global functional analyses, network analyses, and canonical pathway analyses.
For differentially expressed global protein samples, peptide sample of each gel piece was individually analyzed on MS. After searching against protein sequence database, nine sets of data were merged. Above experimental process was repeated thrice; data were merged and then uploaded to IPA for analysis.

Cell proliferation assay
HUVECs were seeded in 96-well plate at a density of 3,000 cells per well. After overnight serum starvation, cells were incubated in DMEM containing 2% FBS and different ephrin-B2/Fc concentrations at 37 °C and 5% CO 2 . Cell proliferation was measured using CCK-8 following manufacturer's instructions at indicated times (1, 3, 5, and 7 days). PBS was used in control group. Eight repetitive wells were set for each group.

Cell cycle analysis
After 24 h of serum starvation, HUVECs were cultured in DMEM containing 2% FBS and 1 μg/mL ephrin-B2/Fc at 37 °C for 24 h. Cells were then harvested and fixed in 70% pre-cooled ethanol at 4 °C. After incubation with 100 mg/L RNase A at 37 °C for 30 min, 50 mg/L propidium iodide was added into suspended cells in the dark for 30 min at room temperature. More than 10,000 cells in each sample were analyzed by flow cytometry (Bacton Dickson Co.), and data were analyzed using MultiCycle for Windows 32-bit software.

Wound healing assay
HUVECs were seeded on six-well plates and grown to 100% confluence. After 12 h of serum starvation, consistently shaped wounds were made using a sterile 200 μL pipette tip across bottom surfaces of each well, creating cell-free areas. Cultures were gently washed with PBS to remove loose cells. Cells were cultured in serum-free medium containing different ephrin-B2/Fc concentrations or PBS for 24 h, fixed in 4% paraformaldehyde for 20 min, and then stained with crystal violet for 30 min at room temperature. Cell images were captured under an optical microscope. Six different scraped areas of each well were randomly selected, and cell numbers were counted.

Transwell migration assay
Migration assay was performed using Transwell chambers (8 μm in pore size, Corning). A total of 400 μL serum-free DMEM containing different ephrin-B2/Fc concentrations was added to the lower chamber, whereas 3.5 × 10 4 cells in 200 μL of DMEM were planted onto the upper chamber. Cells were cultured for 6 h at 37 °C under humidified 5% CO 2 atmosphere. Cells in upper chamber were tenderly removed using wet cotton swabs, whereas lower cells were fixed with 4% paraformaldehyde for 20 min and stained with crystal violet for 30 min. Micrographs of six fields were randomly obtained under an inverted microscope, and cells were counted. Three independent experiments were performed thrice.

Cell survival ratios assay
HUVECs were cultured in serum-free medium containing different concentrations of H 2 O 2 for 4 h. Survival ratios were tested by CCK-8 assay according to instruction. Next, cells cultured in serum-free medium were incubated within PBS or different concentrations (0.1, 0.3, and 1 μg/mL) of ephrin-B2/Fc for 2 h, then 0.3 mmol/L H 2 O 2 was added for another 4 h. Cell survival ratios were also tested using CCK-8 kit.

Western blot
Cells were treated with different ephrin-B2/ Fc concentrations for 0, 5, 20, and 60 min and 3 h and were lysed with RIPA buffer supplemented with protease inhibitors. Protein concentrations were measured using bicinchoninic acid (BCA) method. Equal amounts of proteins were separated with SDS-PAGE and then electrophoretically transferred to nitrocellulose membranes. Membranes were blocked in 5% bovine serum albumin for 1 h at room temperature and then incubated overnight with primary antibodies diluted in Tris-buffered saline with Tween-20 (TBS-T) at 4 °C. All primary antibodies were diluted at 1:1000 except for anti-c-Myc antibody, which was diluted at ratio of 1:800. Membranes were washed thrice with TBS-T buffer and incubated with corresponding secondary antibodies diluted (1:5000) in TBS-T. Bound antibodies were detected through chemiluminescence (Pierce). Quantity One (version 4.4) was used for quantitative analysis.

Data analysis and statistics
All assays were performed in three separate experiments conducted in triplicate. Results were reported as mean ± standard error of the mean (SEM) of three independent experiments. Comparisons were performed using two-tailed paired Student's t-test. *p < 0.05, **p < 0.01, and ***p < 0.001.