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EGCG Regulates Cell Apoptosis of Human Umbilical Vein Endothelial Cells Grown on 316L Stainless Steel for Stent Implantation

Authors Wang J, Wang Y, Zhao Y, Zhao J, Zhang B, Xu K

Received 9 December 2020

Accepted for publication 21 January 2021

Published 11 February 2021 Volume 2021:15 Pages 493—499

DOI https://doi.org/10.2147/DDDT.S296548

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3

Editor who approved publication: Dr Anastasios Lymperopoulos

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Jinpeng Wang,1 Yue Wang,2 Yuyi Zhao,2 Jinbin Zhao,2 Beilin Zhang,3 Kun Xu2,4

1Department of Cardiology, The Second Hospital of Jilin University, Changchun, 130041, People’s Republic of China; 2Department of Nutrition and Food Hygiene, School of Public Health, Jilin University, Changchun, 130021, People’s Republic of China; 3Department of Physiology, College of Basic Medical Sciences, Jilin University, Changchun, 130021, People’s Republic of China; 4Jilin Engineering Research Center of Public Health Detection, Changchun, 130021, People’s Republic of China

Correspondence: Kun Xu
Department of Nutrition and Food Hygiene, School of Public Health, Jilin University, Changchun, 130021, People’s Republic of China
Email [email protected]

Background: Nowadays, medical grade 316L stainless steel (316L SS) is being widely used for intravascular stents, and the drug-eluting stent (DES) system is able to significantly reduce the occurrences of in-stent restenosis. But the drugs and the polymer coating used in DES potentially induce the forming of late stent thrombosis. In order to reduce the occurrence of ISR after stent implantation, the development of novel drugs for DESs is urgently needed.
Methods: This study aimed to investigate the potential mechanisms of epigallocatechin-3-gallate (EGCG) on human umbilical vein endothelial cells (HUVEC) grown on 316L stainless steel (316L SS) using flow cytometry and Q-PCR methods.
Results: Our results showed that EGCG (12.5, 25, 50, 100 μmol/L) significantly inhibited HUVEC proliferation. Flow cytometry analysis indicated that EGCG (25, 50, 100 μmol/L) induced apoptosis. Moreover, qRT-PCRrevealed that genes associated with cell apoptosis (caspase-3, 8, 9, Fas) and autophagy (Atg 5, Atg 7, Atg 12) were up-regulated after EGCG treatment.
Conclusion: These findings indicate that EGCG possesses chemo preventive potential in stent coating which may serve as a novel new drug for stent implantation.

Keywords: EGCG, 316 stainless steel, HUVECs, apoptosis

Introduction

Coronary artery disease (CAD), commonly caused by atherosclerosis, is becoming one of the leading causes of mortality worldwide, especially in developed countries. The vascular stent is the most commonly used technique for the treatment of severe cases of CAD. However, restenosis and thrombosis are commonly occurring complications of this technique. In clinic, more than 20% of patients who received stent implantation developed in-stent restenosis (ISR).1 This phenomenon is only avoided when patients are treated with routine anticoagulation therapies. Thrombosis occurs due to insufficient re-endothelialization of the vascular stent surfaces after stent implantation. Nowadays, medical grade 316L stainless steel (316L SS) is being widely used for intravascular stents, due to its suitable mechanical properties and outstanding anti-corrosion abilities. Meanwhile, immobilization of organic molecules on the surface of the metal is difficult due to the lack of surface reactive groups.

Drug-eluting stent (DES) system is an important milestone in the development of coronary intervention therapy, as the use of DES is able to significantly reduce the occurrences of ISR.2,3 Simultaneously, the drugs and the polymer coating used in DES cause the delay of endothelialization and the healing process, which potentially induce the forming of late stent thrombosis (LST).4–6 Early neo-atherosclerosis observed with the newest DES designs was associated with the incidence of spontaneous myocardial infarction at late outcome.7 Additionally, there is evidence that DES designs also induce endothelial dysfunction that may be associated with long-term cardiac and non-cardiac adverse events, such as solid tumors.8

In order to reduce LST and anti-tumor after stent implantation, the development of novel drugs for DESs is urgently needed. Epigallocatechin-3-gallate (EGCG) is abundantly present in green tea and has been intensively studied for its biological and pharmacological effects, including anti-oxidation, anti-tumor, anti-infection, anti-inflammation, and pro-apoptosis.9–16

In previous studies, EGCG treatments were demonstrated to inhibit proliferation and enhance apoptosis in cancer and other types of cell.17,18 EGCG has also been found to inhibit the proliferation of smooth muscle cells through the effects of p53 and NF-κB signaling pathways.19 Moreover, EGCG demonstrates protective effects during ischemia-reperfusion (I/R) injuries and apoptosis. Especially, EGCG has been found to have beneficial effects during I/R injuries of the heart through the suppression of STAT1 phosphorylation.20 For those reasons, in this study, we aimed to investigate the potential effects of EGCG on modulating proliferation, apoptosis, and related signaling pathways of human umbilical vein endothelial cells (HUVECs) on 316L SS.

In this study, we provided novel evidence of the effects and intracellular mechanisms of EGCG on the proliferation of HUVECs through 316L SS co-culturing and investigated the potential application of EGCG as an inhibitory drug on the coating of DES to reduce the occurrence of ISR.

Materials and Methods

Materials

316L SS materials (C: 0.025; Cr: 17.5; Mn: 1.06; Mo: 2.66; Ni: 13.07; Si: 0.6; S: 0.008; P: 0.02wt% and Fe in balance) were machined into Ф32×1mm. All materials were merged in 75% ethanol and ultrasonically cleaned, rinsed with sterile water, and disinfected at 121°C for 20 min.

Groups

HUVECs cultured on the surface of 316L SS were divided into five groups: 316L group (without EGCG); 316L+EGCG (12.5μmol/L); 316L +EGCG (25μmol/L); 316L +EGCG (50μmol/L); 316L +EGCG (100μmol/L). Untreated cells cultured without 316L SS were used as the control group.

Cell Culture

HUVECs were purchased from KeyGen biotech company (No: KG330, KeyGen, Jiangsu, China) and cultured with DMEM (Hyclone, China) with 10% fetal bovine serum (FBS) (Gibco, USA), penicillin (100 IU/mL), and streptomycin (100 μg/mL) in a cell incubator (CO2, 5%) at 37°C.

Cell Adhesion

HUVECs (5×105cells/mL) were plated on 316L SS in 6-well cell plates (Thermo Fisher Scientific, USA), and incubated for 4 h. The 316L SS plates were carefully rinsed with cell medium and then washed with phosphate-buffered saline (PBS) buffer X2. Adhered cells were digested with 0.25% trypsin (Gibco, USA), and counted using trypan blue under a microscope.

Observation of Cell Morphology

HUVECs (20,000 cells/mL) were labeled with calcein AM (dissolved in ethanol, dye for living cells), plated in 6-well cell plates (without or with the EGCG treatments at 12.5, 25, 50, 100 μm/L), and incubated for 3 days. The viabilities of HUVECs were evaluated by fluorescence microscopy (Olympus IX81, Japan).

Apoptosis Assessment by Flow Cytometry

HUVECs (5000 cells/mL) were plated on 316L SS and cultured for 7 days. Cells were freshly harvested, washed with PBS buffer X2, and resuspended with AnnexinV-FITC and PI (Beyotime Biotechnology, China) buffer for 15 min at room temperature (avoiding light). In flow cytometry, apoptotic cells were marked with Annexin V+/PI- (early apoptotic) or Annexin V+/PI+ (late apoptotic). Annexin-V can bind to phosphatidylserine which is everted on the cell surface in the presence of calcium ion, and eversion of phosphatidylserine is an early stage of apoptosis.

PI is a kind of DNA dye. In the late stage of apoptosis, the permeability of the cell membrane increases, PI enters the nucleus and binds to DNA. Flowjo software (Becton, Dickinson and Company, USA) was used for the analysis.

Quantitative Real-Time PCR

HUVECs (5000 cells/mL) were plated on 316L SS and cultured for 7 days. Total RNA was harvested by TRIzol reagent (Invitrogen, USA) and reverse-transcription was used to obtain cDNA by using reverse transcription (RT) reagents (Takara Biotechnology Co., Ltd., China). Target sequences were amplified by quantitative real-time PCR (qRT-PCR) using SYBR Premix Ex Taq II (Takara Biotechnology Co., Ltd., China) on a Real-Time PCR system (ABI prism 7500, Applied Biosystems, Foster City, USA) platform. Primers for qRT-PCR are listed in Table 1. All data were analyzed based on -ΔΔCt method. GAPDH was used as the internal control.

Table 1 The Primer Sequence of Target Gene

Statistical Analysis

Data analysis was carried out by SPSS software (Chicago, USA). All data were displayed as means± standard deviation (SD) (n= 3). One-way analysis of variance (ANOVA) followed by least significant difference (LSD) was used for statistical analysis. Rank sum test was used for nonparametric analysis. P value <0.05 was considered as statistically significant.

Result

Effect of EGCG on HUVECs on 316L SS Surface

As shown in Figure 1, the proliferation of HUVECs on the 316L SS surface was observed. As a result, HUVECs were distributed as monolayers with no significant difference in cell morphology observed between cells on 316L SS and control. Living cell numbers in both the 316L SS group and EGCG treated group were elevated with time. Densities of HUVECs on 316 L SS surface were observed as the highest compared with both control and EGCG treated groups.

Figure 1 Fluorescent images of HUVECs grown on 316L surface. Cultured for 3 days (*40). (A) Control (B) 316L (C) 316L +12.5 μmol/L, (D), 316L+25 μmol/L (E) 316L+50 μmol/L, and (F) 316L+100 μmol/L.

Effect of EGCG on Apoptosis of HUVECs Co-Cultured with 316L SS

Flow cytometry was carried out for the assessment of the effects of EGCG on the apoptosis of HUVECs on 316L SS. (Figure 2). Early apoptotic ratio of HUVECs was 6.79% for the 316L group, which was lower than that of the control group (9.16%). Meanwhile, the apoptotic ratios of the early apoptotic HUVECs were 8.4%, 8.15%, 12.57%, and 34.74% for EGCG treatments of 12.5, 25, 50, and 100 μmol/L, respectively. Later apoptotic ratio of HUVECs was 1.79% for the 316L group, which was lower than that of the control group (2.58%). Later apoptotic ratios of HUVECs were 3.92%, 2.62%, 4.89%, and 9.85% for EGCG treatments of 12.5, 25, 50, and 100 μmol/L, respectively.

Figure 2 Flow cytometry analysis of apoptosis of HUVECs. Cells were cultured on 316L SS surface without or with EGCG treatments (12.5, 25, 50, 100μmol/L) for 3 days. Annexin-V positive PI negative represents the proportion of early apoptotic cells; quadrant of early apoptotic stage was in right lower quadrant. Annexin-V positive PI-positive cells represent the late apoptotic or necrotic cells. Quadrant of late apoptotic cells was in the right upper quadrant.

Effect of EGCG on Apoptotic Genes of HUVECs Co-Cultured with 316L SS

The mitochondrial pathway, featured by the activation of caspase-9, is closely related to the regulations of apoptosis.21 The relative mRNA expressions of Caspase-3 and Caspase-9 in the EGCG (25, 50, 100 μm/L) treated group were increased compared with the 316L group. The relative mRNA expressions of Caspase-8 and Fas in the EGCG (12.5, 25, 50, 100 μm/L) group were also increased compared with the 316L group (Figure 3A).

Figure 3 Gene expression profiles of HUVECs. (A) Shows apoptotic genes and (B) shows autophagic genes. Data were displayed as mean ± SD. *P < 0.05 compared with 316L group.

Effect of EGCG on Autophagy of HUVECs Co-Cultured with 316L SS

The qRT-PCR analysis demonstrated that the expressions of regulator genes of autophagy: ATG5, ATG7, and ATG12, were increased in HUVECs on the 316L SS surface, indicating the activation of autophagy. Moreover, EGCG (25, 50, 100 μmol/L) enhanced the expression of ATG5, ATG7, and ATG12 in HUVECS co-cultured with 316L SS (Figure 3B).

Discussion

Our results showed that EGCG (12.5, 25, 50, 100 μmol/L) significantly inhibited HUVEC proliferation. Flow cytometry analysis indicated that EGCG (25, 50, 100 μmol/L) induced apoptosis. Moreover, as revealed by qRT-PCR, we found that the expressions of genes associated with cell apoptosis (caspase 3, caspase 8, caspase 9 and Fas) and autophagy (Atg 5, Atg 7, Atg 12) were up-regulated after EGCG treatments.

Vascular stent implantation is a widely acknowledged method for the clinical treatment of arterial trauma. However, the naked surface of the metallic stent also potentially acts as a stimulus promoting allergies and inflammation. A large number of epidemiological studies have suggested that green tea can exert an anti-cancer effect on a variety of tumor cells, and long-term consumption of green tea reduces the risks of various cancers. EGCG enhances autophagy through the promotion of autophagosome formation, the enhancement of lysosomal acidification, and the stimulation of autophagic flux in Müller cells.22 Li et al demonstrated that HUVECs exposed to 316L SS could cause cell proliferation compared with the medium group.23 In this study, our cell morphology results showed higher living cell numbers of HUVECs on the 316L SS surface than in the controls. Furthermore, the treatments with EGCG (12.5, 25, 50, 100 μm/L) significantly reduced the number of HUVECs on 316L SS surface. Our results were consistent with the findings of Zhang et al, where EGCG treatments were demonstrated to inhibit cell proliferation during I/R injuries.24

To investigate the underlying mechanisms of the inhibitory effects of EGCG treatments on cell proliferation on 316L SS surface, flow cytometry analysis was performed. In the results of flow cytometry, it was shown that EGCG (25, 50, 100 μmol/L) treatments promoted the apoptosis of HUVECs compared with the 316 L group. Apoptosis is mainly induced through two approaches. One of them is through the activation of caspase by extracellular stimulus and the Fas-dependent pathway. Fas belongs to the transmembrane protein of the tumor necrosis factor receptor superfamily. Fas is able to bind with its ligand FasL and initiate signal transductions, which activate caspase-8 and the signaling cascades, which subsequently leads to the induction of apoptosis. Another approach for apoptosis induction is through the release of apoptosis protease activating factor (Apaf) by mitochondria, which leads to the activation of caspase. Stimulations such as stress and apoptotic signals cause the release of cytochrome C by cells. With the existence of dATP, extracellular cytochrome C forms polymers with Apaf-1, and enhances the formation of apoptotic bodies with caspase-9. Subsequently, caspase-9 is activated. Its activation also induces the activations of other caspases such as caspase-3, and thus causes the apoptosis of cells.25,26 Autophagy happens during conditions such as nutrient deprivation and stress responses, in order to promote the survival of cells. Four autophagy-related genes were discovered in the studies of yeast, and have been proven to play critical roles in the induction, processing, maturation, and recycling of autophagy. Atg5 is widely accepted as a key component in the mechanisms of autophagy. Atg5 contributes to the process of ubiquitin-like conjugation system, which is indispensable during the pre-autophagosomal structure elongation process. Atg12 is an ubiquitin-like protein, able to bind with Atg5 through covalent bonds, under the facilitation of Atg7 and Atg10. This Atg12-Atg5 heterodimer subsequently binds with Atg16Land forms a multi-protein complex.27 Meanwhile, autophagy and apoptosis are closely associated processes rather than isolated. Caspase-8 has been found to participate in the regulation of autophagy, while Atg5 has also been found to interact with Fas-associating protein with a novel death domain (FADD) and induce apoptosis.28,29 In this study, we found that 7 days after the EGCG treatments (except for low dose treatment at 12.5mol/L), the expressions of caspase-3 were found to be higher than that in the 316L SS group. Meanwhile, as revealed by higher expression levels of caspase-8, caspase-9, Atg 5, Atg7, and Atg12, EGCG treatments (at all treatment doses) were demonstrated to inhibit the proliferation of cells on 316L SS surface through the promotion of both autophagy and apoptosis.

However, the mechanisms involved in 316L material for the growth of HUVECs are complex, as is the function of EGCG; therefore, further research is required.

Conclusion

In this study, we demonstrated the effects of EGCG on HUVECs’ growth on 316L SS surface. EGCG (12.5, 25, 50, 100 μmol/L) significantly inhibited HUVEC cell proliferation. As revealed by flow cytometry, EGCG promoted the apoptosis of cells growing on 316L SS surface. The gene expression profile of HUVECs was analyzed by qRT-PCR and indicated promoted cell apoptosis and autophagy caused by EGCG treatment, as revealed by higher gene expression levels of genes related to both apoptosis and autophagy. Our results provided robust evidence suggesting that EGCG promoted the apoptosis of endothelial cells through the regulation of apoptotic and autophagic genes. These results and conclusions established solid foundations for the new drug development of stent applications. However, further in vivo studies for the validation of our conclusions are necessary.

Acknowledgment

This work was financially supported by the Jilin Province Development and Reform Commission (grant number: 2020C038-7), the Development of Science and Technology, Jilin Province, China (grant number: 2018010195JC), National Natural Science Foundation of China (grant number: 81401721), the Education Department of Jilin Province, China (grant number: JJKH20180239KJ), and the Health and Family Planning Commission of Jilin Province (grant number: 2017J074). There is no conflict to declare regarding funding.

Disclosure

We declare that there are no financial or other contractual agreements that may cause conflicts of interest or be perceived as causing conflicts of interest.

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