The conventional photosensitizers used in photodynamic therapy (PDT), such as haematoporphyrin (HP), have not yet reached satisfactory therapeutic effects on port-wine stains (PWSs), due largely to the long-term dark toxicity. Previously we have showed that hypericin exhibited potent photocytotoxic effects on Roman chicken cockscomb model of PWSs. However, the molecular mechanism of hypericin-mediated photocytotoxicity remains unclear. In this study, we employed human umbilical vein endothelial cells (HUVECs) to investigate the hypericin-photolytic mechanism. Our study showed that hypericin-PDT induced reactive oxygen species (ROS), resulting in cell killings and an activation of the inflammatory response. Importantly, we have also discovered that photoactivated hypericin induced apoptosis by activating the mitochondrial caspase pathway and inhibiting the activation of the vascular endothelial growth factor-A (VEGF-A)-mediated PI3K/Akt pathway. Notably, we found that hypericin exhibited a more potent photocytotoxic effect than HP, and largely addressed the inconvenience issue associated with the use of HP. Thereby, hypericin may be a better alternative to HP in treating PWSs.
Port-wine stains (PWSs) are a congenital form of vascular malformation that are characterized by ectatic capillaries and postcapillary venules in the papillary and mid-reticular layers of the dermis, often occurring on the face and neck. PWSs are the most common type of vascular malformation, with a prevalence of approximately 0.3% in newborns1,2. Over time, the diameters of the vessels would progress, resulting in clinical condition and even a disfiguring lesion3. It is estimated that two-thirds of patients would develop hypertrophic or nodular lesions by the age of fifty4,5,6.
Recently, photodynamic therapy (PDT) has been successfully used to treat PWS lesions7,8. The process involves the use of a photosensitizer, light and molecular oxygen. Nonetheless, the photosensitizer is a critical factor in effective treatment, which reacts with molecular oxygen to produce cytotoxic reactive oxygen species (ROS) to destroy the diseased tissue9. Current studies have focused on identifying satisfactory photosensitizer drugs, such as haematoporphyrin and its derivatives. However, the half-life of haematoporphyrin and its derivatives are very long and the fluorescence can still be detected even after a year following the intravenous infusion10,11. This long half-life can lead to many complications, such as dark toxicity, due to the prolonged skin photosensitivity to sunshine and visible light. Consequently, when administered with haematoporphyrin or their derivatives, patients are required to avoid sun exposure for up to 4 weeks12,13. This poor patient compliance has adversely limited their clinic applications14.
Hypericin is a naturally occurring photosensitizer extracted from a plant of Hypericum perforatum (St. John’s Wort)15. It exhibits high ROS yields (0.17–0.80)16,17. Studies have shown that hypericin is a selective anti-tumour photosensitizer17. And many studies have revealed that its anti-tumour properties are mediated by autophagy and immune responses18,19,20,21,22. However, a few studies have been conducted which indicated that treating effects of hypericin on vascular injury and the elimination of malformed capillaries23. For example, our previous investigations first revealed that hypericin was used in treatment of PWSs using a chicken comb model, and good therapeutic effect was obtained24. This result is very exciting, especially when considering that the half-lives of hypericin is only 27 h even at a dosage of 1500 μg/kg25. The much shorter half-life of hypericin has therefore largely addressed the inconvenience issue associated with the use of other photosensitizers. The great potential of hypericin as an excellent alternative photosensitizer therefore prompted us to further explore its reaction mechanism.
In this study, human umbilical vein endothelial cells (HUVECs) were used as the model to investigate how hypericin induces photocytotoxicity. We found that hypericin induced apoptosis in HUVECs. Specifically, we evaluated the effects of hypericin on the mitochondrial apoptotic pathway and the VEGF-A-mediated PI3K/Akt pathway. We discovered that hypericin induced apoptosis via Bax/Bcl-2 ratio upregulation, ΔΨm collapse, accompanied with cyto c release, procaspase-3, procaspase-9 and PARP cleavage, and also VEGF-A suppression, p-Akt inhibition and Bad dephosphorylation. The efficacy of hypericin was also compared to haematoporphyrin. Hypericin exhibited a more potent photocytotoxic effect on the above-mentioned pathways than haematoporphyrin. These findings provide a novel mechanistic basis for the application of hypericin in the treatment of PWSs.
Materials and Methods
Hypericin (HY) was purchased from Chengdu Biopurify Phytochemicals (batch no. 081204, purity 99.1%, Chengdu, China). HY was dissolved in dimethylsulfoxide (DMSO, Sigma-Aldrich Co., St Louis, MO) to produce a stock solution (3.2 mM) for the in vitro assays. Haematoporphyrin (HP) was obtained from Shanghai Red and Green Photosensitizer Institute (Shanghai, China) and dissolved in DMSO to produce a stock solution (1.6 mM) for the in vitro assays. The HY and HP stock solutions were stored at −20 °C and diluted to the final concentration using complete Roswell Park Memorial Institute 1640 (RPMI-1640, New Mexico, USA) medium before use. zVAD-fmk was obtained from Selleck Chemicals (Houston, USA) and Bax-Inhibiting Peptide (BIP) was purchased from Merck Millipore (Hesse-Darmstadt, GER). VEGF-A (vascular endothelial growth factor-A) was obtained from Cell Signaling Technology (CST, Boston, USA).
Cell lines and cell culture
Human umbilical vein endothelial cells (HUVECs) were obtained from American Type Culture Collection (Rockefeller, Maryland, USA). The cells were incubated in complete RPMI-1640 medium supplemented with 10% (v/v) heat-inactivated foetal bovine serum, 2 mM L-glutamine and a penicillin-streptomycin solution (100 U/ml penicillin and 100 μg/ml streptomycin) at 37 °C with 5% CO2 and 95% air in a humidified atmosphere.
In vitro PDT treatment
PDT was performed on HUVECs seeded into cell culture plate. After an overnight incubation, the media were replaced with fresh media containing increasing concentrations of HY or HP. The cells were then incubated for 24 h in the dark. After replacing the media, the cells were then irradiated using a 585-nm LED light (YK-LED-PDT; Jiangxi Xinyu Shunxing Technology Development Co., Jiangxi, China) at a dose of 1.0 J/cm2. The HUVECs treated in the same way in the absence of the PS drugs (HY or HP) were used as the vehicle control.
The HUVECs were pretreated with the pan-caspase inhibitor zVAD-fmk (20 μM) or the more specific Bax inhibitor BIP (100 μM) for 3 h followed by treatment with HY (0.062 μM) in combination with the inhibitor for 24 h. Then the cells PDT-treated were cultured for 24 h. The HUVECs treated in the same way in the absence of HY were used as the zVAD-fmk/BIP control.
The HUVECs were serum-starved for 24 h and stimulated with VEGF-A (25 ng/ml) in fresh medium. The cells were then incubated with media containing HY (0.062 μM) and VEGF-A (25 ng/ml) for 24 h; the PDT-treated cells were cultured for an additional 24 h. The cells were lysed and the proteins were harvested for western blot analysis.
Observation of the morphological changes
The HUVECs were seeded onto a 6-well plate (1.5 × 105 cells per well). The HUVECs treated in a similar manner but without light irradiation (i.e., PSs treatment without light irradiation (Non-PDT)) were used as controls. The changes in the celluar morphology were observed using an inverted microscope (Olympus, TAKACHIHO SEISAKUSHO, Japan).
Cell viability assays
MTT assays were conducted to determine the photocytotoxic effects of HY on HUVECs. The cells were divided into two groups (PDT or Non-PDT group). Approximately 5.0 × 103 cells were seeded onto 96-well plates. After an overnight growth, the cells were treated with increasing concentrations of HY (0.016, 0.031, 0.062, 0.125, 0.250, and 0.500 μM) and HP (2 μM) for 24 h. The culture media were removed and replaced with fresh media. One group of cells (PDT group) was then exposed to a 585-nm LED light at a dose of 1.0 J/cm2. The other group (Non-PDT group) was not treated with light irradiation. Afterwards, both groups were incubated for an additional 24 h in the dark. Then, 5 mg/ml MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide, Sigma-Aldrich Co., St Louis, MO) was added to each well, and the cells were incubated for another 4 h as previously described. The cell viability of the treated cells was compared with that of the vehicle-only control cells (100%) to calculate the IC50 value.
DAPI staining assay
The HUVECs were seeded onto a 6-well plate (2 × 105 cells per well) before the PDT treatment. After treatment, the media were aspirated and the cells were fixed with 4% paraformaldehyde for 5 min. The fixed cells were then washed twice with phosphate-buffered saline (PBS) and stained with DAPI (4′,6-diamidino-2-phenylindole, Beyotime, Shanghai, China) for 5 min at room temperature. After three washes with PBS times, the condensed chromatin and fragmented nuclei in DAPI-stained apoptotic cells were viewed under a fluorescence microscope (Nikon Co., Japan; magnification: ×400).
The HUVECs were seeded onto a 6-well plate (2 × 105 cells per well). The irradiated cells were then harvested after the PDT treatment. The early apoptotic cells (Annexin V-FITC+/PI−), late apoptotic cells and dead cells (Annexin V-FITC+/PI+) were quantitatively estimated using a FACScan flow cytometer (FACSVantage SE, Becton-Dickinson, New Jersey, USA) using the Annexin V-FITC and PI apoptosis detection kit (Beyotime, Shanghai, China).
Quantification of the secreted TNF-α, IL-6, IFN-γ, IL-1β and IL-10 levels using ELISAs
The HUVECs were seeded onto a 24-well plate (2.0 × 104 per well) before the PDT treatment. The cell culture supernatants were then collected and filtered through a 0.22-μm Steriflip filter (Millipore, Massachusetts, USA). The concentrations of TNF-α, IL-6, IFN-γ, IL-1β and IL-10 were quantified using the Human ELISA Kit (BOSTER, Wuhan, China) following the manufacturer’s instructions.
Measurement of the intracellular ROS levels
The ROS levels were measured using the Reactive Oxygen Species Assay Kit (Beyotime, Shanghai, China) following the manufacturer’s instructions. Intracellular ROS production was assessed by measuring the oxidized dichlorofluorescein (DCF) levels in the HUVECs. The non-fluorescent probe 2′,7′-dichlorofluorescein diacetate (DCFH-DA) diffuses into the cells, where it is deacetylated to non-fluorescent 2′,7′-dichlorofluorescein (DCFH). Subsequently, DCFH is oxidized by the intracellular ROS to the fluorescent product DCF. The cells were seeded onto a 6-well plate (2 × 105 cells per well) before the PDT treatment. The irradiated cells were then harvested and incubated with DCFH-DA (25 μM) for 45 min at 37 °C in the dark. Afterwards, the DCFH-DA was removed and the cells were washed three times with PBS. The fluorescence was read at 485 nm (excitation) and 535 nm (emission) with a fluorescence spectrophotometer (Hitachi, Ltd, Japan).
Mitochondrial membrane potential (ΔΨm) assay
The ΔΨm was measured using the mitochondrial membrane potential assay kit with JC-1 (5,5′,6,6′-tetrachloro-1,1′,3,3-tetraethylbenzimidazole-carbocyanide iodine, Beyotime, Shanghai, China) following the manufacturer’s instructions, using a fluorescence microscope (Nikon Co., Japan; magnification x400). The HUVECs were seeded onto a 6-well plate (2 × 105 cells per well) before the PDT treatment. Afterwards, the cultured cells were stained with JC-1 (10 μg/ml) for 30 min at 37 °C and washed twice with ice-cold PBS. The cells incubated with carbonyl cyanide m-chlorophenylhydrazone (protonophore, CCCP, 10 μM) were used as the positive control because CCCP effectively causes ΔΨm depletion. The excitation and emission wavelengths were 510 nm and 527 nm, respectively, for the detection of the monomeric form of JC-1 (green fluorescence). The excitation and emission wavelengths of 580 nm and 590 nm, respectively, were used to detect JC-1 aggregation (red fluorescence). The ratio of red (i.e., the aggregated form of JC-1) to green (i.e., the monomeric form of JC-1) fluorescence intensity, which represented the ΔΨm of HUVECs, was normalized to that of the vehicle control (100%). The fluorescence intensity was evaluated using the ImageJ 2 × software (National Institutes of Health, USA).
Western blot analysis
The cells were grown on a 6-well plate (2 × 105 cells per well) before the PDT treatment. After treatment, the media were aspirated and the cells were washed twice with ice-cold PBS. The proteins were harvested from the cells using cell lysis buffer containing 1 mM PMSF (Beyotime, Shanghai, China). The protein concentrations were measured using the BCA Protein Assay Kit (Beyotime, Shanghai, China).
The proteins were separated by 10% or 12% (for Bcl-2, Bax, cleaved caspase-9, procaspase-3, cleaved PARP, VEGF-A, phospho-Akt (Ser473, p-Akt), Akt, Bad and β-Actin) SDS-polyacrylamide gels and electrophoretically transferred onto PVDF membranes (Millipore, Massachusetts, USA). The membranes were blocked with 6% non-fat milk at 37 °C for 1 h and then incubated overnight with the corresponding primary antibodies at 4 °C. The following antibodies were used in this study: anti-Bcl-2 (1:500, CST, Boston, USA), anti-Bax (1:500, CST, Boston, USA), monoclonal anti-cleaved caspase-9 (1:1000, CST, Boston, USA), monoclonal anti-procaspase-3 (1:5000; Abcam, Cambridge Science Park, UK), anti-cleaved PARP (1:500; CST, USA), polyclonal anti-VEGF-A (1:500, Abcam, Cambridge Science Park, UK), monoclonal anti-p-Akt (Ser473,1:500, CST, USA), anti-Akt (1:500, CST, USA), polyclonal anti-Bad (1:1000, CST, Boston, USA) and anti-β-Actin (1:1000, CST, Boston, USA). The blots were incubated with peroxidase-conjugated AffiniPure goat anti-rabbit or anti-mouse IgG (1:5000, ZSGB-BIO, Beijing, China) as the secondary antibodies for 1 h at 37 °C. The blots were detected with the Immobilon Western Chemiluminescent HRP Substrate (Millipore, Massachusetts, USA). The protein levels were quantitated by densitometry using AlphaEaseFC 4.0 software (San Leandro, CA) and then normalized to the vehicle control (100%). β-Actin was used as an internal control.
The HUVECs were grown on a 6-well plate (2 × 105 cells per well) before the PDT treatment. After treatment, the cells were then washed twice with ice-cold PBS. Total RNA was extracted from the PDT-treated cells using an RNAiso Plus Kit (TaKaRa, Tokyo, Japan) following the manufacturer’s instructions. Reverse transcription of the extracted RNA was performed using the PrimeScriptTM RT Reagent Kit with gDNA Eraser (TaKaRa, Tokyo, Japan). Two-step qRT-PCR reactions were performed using SYBR® Premix Ex TaqTM II (TaKaRa, Tokyo, Japan) on a Real-Time qPCR System (Mx3000P, Agilent Stratagene, USA). The primers used in this study are listed in Table 1. The relative fold change in the mRNA expression of the target gene was quantified using the 2−∆∆CT method and the MXProv4.1 software. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as a housekeeping gene. A vehicle-only control was used as a calibrator for quantification.
The data were expressed as means plus or minus standard deviation (means ± S.D.). Statistical analysis was performed by one-way analysis of variance (ANOVA). P < 0.05 was regarded as a statistically significant difference.
Growth inhibition by HY-PDT
As shown in Supplementary Fig. S1, after 24 h the growth of HUVECs treated with PDT treatment were significantly inhibited and down-regulated procaspase-3 and up-regulated cleaved PARP were observed. Thus, the subsequent experiments were implemented exposed to photosensitizer dugs with PDT treatment after 24 h.
To determine whether increasing the concentrations of hypericin (HY) could inhibit the growth of HUVECs, we perform image studies using an inverted microscope, given that cell morphology is an indicator of health in cell culture. During the experiment, we observed a significant morphological change in HUVECs following the HY-PDT. As shown in Fig. 1a, the HUVECs treated with photosensitizer drugs without light irradiation (Non-PDT) had a cobble stone-like shape, and there was no sign of cell apoptosis. In contrast, after PDT treatment with 2 μM haematoporphyrin (HP) and 0.031 μM HY, blebbing was observed on the cell membrane, which is a sign of early apoptosis. Moreover, as the concentration of HY (0.062 and 0.125 μM) was increased, more cells became rounded, shrunken and detached from each other, some floated in the medium. These are prominent morphological signs of apoptosis.
To further study the effect of photosensitizer-PDT on cell viability, the HUVECs were treated with HY or HP-PDT and after 24 h were subjected to the MTT assay. As shown in Fig. 1b, the HUVECs’ viability decreased from 79.5% to 5.2% in the irradiated cells treated with HY concentrations ranging from 0.016 to 0.5 μM (P < 0.05 vs. vehicle control). Statistical analysis indicated that the IC50 value was 0.067 μM. However, the viability of the 2 μM HP-PDT was 81.0%. No significant differences were found between 0.031 μM HY-PDT and 2 μM HP-PDT (P > 0.05). The inhibitory effect with increasing concentrations of HY (HY 0.062-0.5 μM) was stronger than that with 2 μM HP. This is very exciting, the low dosage may allow for low toxicity. However, the cell viability was not inhibited in Non-PDT cells (P > 0.05 vs. vehicle control), demonstrating a possible selective treating using HY.
HY-PDT induced apoptosis in HUVECs
To investigate whether the HY-PDT-mediated inhibition of cell growth result from the induction of apoptosis, we examined the characteristics changes in chromatin morphology, which is an indicative sign of apoptosis. The vehicle control cells exhibited homogenous chromatin morphology. After the treatment using HP-PDT and HY-PDT, the cells exhibited the morphological features of apoptotic cells, such as chromatin condensation, marginalization, or nuclear fragmentation (Supplementary Fig. S2a). Specifically, the DNA fragmentation was observed at high concentration of HY (0.125 μM). However, this apoptosis was markedly decreased when pan-caspase inhibitor zVAD-fmk (20 μM), or a more specific Bax inhibitor BIP (100 μM) was added (Fig. 2a). This study suggested that HY-PDT inhibited the growth of HUVECs via induction of apoptosis.
To further confirm the process of HY-PDT-induced apoptosis, flow cytometry was applied to identify the apoptotic cells (Annexin V-FITC+/PI−) and the late apoptotic or dead cells (Annexin V-FITC+/PI+). As shown in Supplementary Fig. S2b, the percentages of apoptotic cells increased to 6.0%, 6.3%, 17.8%, and 48.4% upon the treatment of 0.031, 0.062, 0.125 μM HY and 2 μM HP, respectively, indicating that HY-PDT led to a concentration-dependent increase in the percentage of apoptotic cells. In addition, the number of apoptotic cells increased even further after treatment with higher concentrations of HY (0.062 and 0.125 μM) than with HP (2 μM) (Supplementary Fig. S2c). We found that the percentage of apoptotic cells was strongly reduced in the HUVECs pretreated with z-VAD-fmk or BIP (Fig. 2b,c). Taken together, our studies confirm that HY-PDT induced HUVEC apoptosis, the effect of which displayed a more potent on the inhibition of cell growth via apoptosis.
HY-PDT promoted the inflammatory response in HUVECs
To test the level of inflammatory mediators in HUVECs following PDT, the expression of TNF-α, IL-6 and IFN-γ was determined using ELISAs and qRT-PCR assays. Our studies showed that HY- or HP-PDT strongly enhanced the secretion of TNF-α, IL-6 and IFN-γ (Fig. 3a–c). Similarly, the expression of the TNF-α and IL-6 mRNAs also concentration-dependently and significantly increased, as shown in Fig. 3f. Again, in this case, HY exhibited a more potent effect than 2 μM HP did. Notably, the IL-6 levels were clearly increased compared to the TNF-α and IFN-γ levels. However, the IL-1β and IL-10 levels were inconsistent after PDT and the concentration of IL-1β mostly remained below the detection limit (Fig. 3d,e). These results demonstrate that HY- or HP-PDT treatment promoted the inflammatory response, resulting in the secretion of TNF-α, IL-6, IFN-γ, particularly IL-6, which consequently led to HUVEC death. Additionally, our studies also indicated that HY-PDT exhibited a much more potent effect than HP-PDT in terms of activating the immune response.
HY-PDT enhanced ROS production in HUVECs
Our next goal was to study whether ROS production contributed to the secretions of inflammatory mediators. The ROS production was measured using a fluorescent probe DCFH-DA. As shown in Fig. 4, the level of DCF fluorescence was significantly increased in the HUVECs treated with HY-PDT in a concentration-dependent manner. At higher concentrations (0.062 and 0.125 μM), the fluorescence intensities from HY-PDT were greater than that from 2 μM HP-PDT. These observations indicated that the oxidized DCF levels were high in HUVECs, indicating a high level of ROS production following the HY- or HP-PDT treatment. Taken together, our studies suggest that HY-PDT triggered ROS production, which was more effective than that of HP-PDT.
HY-PDT led to collapse of the ΔΨm in HUVECs
Apoptosis is activated through two major pathways, mitochondrion dependent or independent pathway. The ΔΨm is an indicator of mitochondrial function. To investigate the mechanism of apoptosis, the ΔΨm was examined by fluorescence microscopy. The ratio of red and green fluorescence intensities represented the ΔΨm of HUVECs. CCCP can cause ΔΨm depletion and was, therefore, used as a positive control. As shown in Supplementary Fig. S5a, following PDT with increasing concentrations of HY, the red fluorescence became weaker and the green fluorescence became stronger. As shown in Supplementary Fig. S5b, the ratio of red and green fluorescence intensities decreased significantly upon the treatment of HY-PDT; and the rate of decrease is concentration-dependent, indicating that HY is a potent photosensitizer that leads to collapse of the ΔΨm. Compared with the CCCP control, the ratios of HP and HY at higher concentrations (0.062 and 0.125 μM) were not significantly different (data not shown), indicating that HY- or HP-PDT, could both cause the loss of ΔΨm in HUVECs. However, the specific Bax inhibitor BIP (100 μM) could significantly relieve the HY-induced (0.062 μM) mitochondrial depolarization, as shown in the fluorescent colour change from green to orange-red. This study demonstrated an attenuation of the dissipation of ΔΨm (Fig. 5a,b). Mitochondrial dysfunction has been suggested to be an important factor in the process of apoptosis. Collectively, these results showed that HY-PDT could lead to a significant collapse of ΔΨm and subsequently apoptosis. These findings therefore, indicated that HY can induce apoptosis via a mitochondria-dependent pathway.
Apoptosis was induced via the mitochondrial pathway of caspase activation in HUVECs
To further explore the mechanism underlying the apoptosis, western blot analyses of apoptosis related proteins and qRT-PCR analyses of mRNAs were performed (Fig. 6 and Supplementary Fig. S6). Concentration-dependent down-regulation in the expression of the anti-apoptotic protein Bcl-2 and up-regulation of the pro-apoptotic protein Bax were found in HUVECs following HY- or HP-PDT (Supplementary Fig. S6a). A similar trend in the expression of procaspase-3 and cleaved PARP was observed (Supplementary Fig. S6a,c). An increase of the cleaved caspase-9 protein was also detected in the HY- or HP-treated cells (Fig. S6a,b). These effects were further studied by measuring of the genes involved in apoptosis using qRT-PCR. Our studies revealed that HY- or HP-PDT significantly increased the Bax/Bcl-2 ratio, cyto c and caspase-3 mRNAs (Supplementary Fig. S6d–f). In this study, we have also found that HY-PDT at high concentrations (0.062 and 0.125 μM) was more effective than the 2 μM HP-PDT.
Additionally, we found that both zVAD-fmk and BIP attenuated the HY-induced (0.062 μM) effects on the levels of the Bax/Bcl-2, cleaved caspase-9, proacaspase-3 and cleaved PARP proteins (Fig. 6a–d). Similarly, the mRNA up-regulations of the Bax/Bcl-2 and caspase-3 also decreased by zVAD-fmk or BIP (Fig. 6d,e). These results further confirmed that HY- or HP-PDT induced apoptosis through the mitochondrial caspase pathway, which was initiated by an increase in the Bax/Bcl-2 ratio, resulting in a loss of ΔΨm (Fig. 5), leading to simultaneous release of cyto c to further activate caspases (caspase-9 and caspase-3), and eventually resulting in PARP cleavage.
HY-PDT blocked the PI3K/Akt (phosphatidylinositol 3-kinase/protein kinase B) pathway
The PI3K/Akt signalling pathway has been shown to be a vital survival signalling pathway and is induced by VEGF-A26. Studies have shown that VEGF suppression can inhibit carcinoma cell proliferation27,28. To investigate whether HY-PDT can interfere the PI3K/Akt pathway, the expression of VEGF-A, p-Akt, and total Akt proteins, the expression of protein and mRNA for the downstream (effector), as well as Bad, were measured (Fig. 7 and Supplementary Fig. S7). Compared to the vehicle control, the expression of the VEGF-A, total Akt and p-Akt (p-Akt/Akt ratio) proteins all decreased in concentration-dependent manner (Supplementary Fig. S7a–c). We also found that the value of Bad increased in a concentration-dependent manner at the transcriptional level and the translational level (Supplementary Fig. S7a,d,e). Moreover, HY-PDT (0.062 and 0.125 μM) was more effective against the above-mentioned effectors compared to 2 μM HP (Supplementary Fig. S7).
Similarly, as shown in Fig. 7, VEGF-A (25 ng/ml) significantly attenuated the HY-PDT-induced (0.062 μM) decrease in the expression of the VEGF-A, the total Akt and p-Akt (p-Akt/Akt ratio) proteins and Bad activation (Fig. 7a–c). These results suggested that HY- and HP-PDT were able to suppress VEGF-A expression, thereby inhibiting Akt activation, and consequently leading to the increase in Bad expression. These studies supported the hypothesis that HY-PDT inhibited the VEGF-A-mediated PI3K/Akt pathway, which involves alternative mechanisms to inhibit cell growth.
HY-PDT induced cell death in HUVECs
The above results suggested that cell death mechanisms underlie the role of HY-PDT in HUVECs. HY, a lipophilic polycyclic quinine, preferentially localizes at the cell membrane29 and specifically accumulates in mitochondria30. In the presence of molecular oxygen, HY can be activated by yellow light at 585 nm to generate cytotoxic ROS, inducing cell killing. These events activate the inflammatory responses and induce apoptosis. The detail reaction mechanism is shown in Fig. 8.
The inflammatory responses subsequently trigger the secretion of TNF-α, IL-6 and IFN-γ, which facilitate long-lasting immunity and the suppression of HUVECs growth. Additionally, HY-PDT also induces HUVEC cell apoptosis via mitochondrial apoptotic pathway. The activation of Bax, the suppression of Bcl-2 results in mitochondrial dysfunction. Furthermore, the increased of mitochondrial membrane permeability, accompanied with the release of cyto c, further activates caspase-9 and the downstream effector caspase-3, and eventually cause the PARP cleavage. Finally, HY-PDT could inhibit HUVEC growth by preventing the activation of the the VEGF-A-mediated PI3K/Akt pathway, which is initiated by suppressing VEGF-A expression. This, in turn, down-regulates the levels of the total Akt and p-Akt proteins to inhibit Akt activation, and stimulates the dephosphorylation of Bad, leading to the release of cyto c. On the other hand, the suppression of p-Akt may also activate downstream caspases; and ultimately cellular apoptosis occurs. Together, HY-PDT induces apoptosis via activating the mitochondrial-mediated caspase pathway and inhibiting the VEGF-A-mediated PI3K/Akt pathway activation. In conclusion, our studies suggested that HY-PDT can trigger cell death through a cascade of events including direct cell killing, activation of the inflammatory responses and induction of apoptosis.
In this study, HUVECs were used to explore the photocytotoxic effects of hypericin (HY). Our results showed HY had a very potent inhibiting effect on HUVECs at very low concentrations. Meanwhile, the mechanism of the HY-mediated photocytotoxicity was proposed as followed: First, HY is activated by yellow light at 585 nm, which has a strong penetrating ability for efficient absorption by HY15,31, in the presence of molecular oxygen, and cytotoxic ROS was generated. It kills the cells and triggers an inflammatory response, leading to the rapid secretion of inflammatory mediators, such as TNF-α, IL-6 and IFN-γ, and particularly IL-6. Subsequently, the secondary inflammatory mediators may recruit DCs, macrophages and neutrophils32; this events facilitate long-lasting immune suppression of HUVEC growth. Additionally, photoactivated HY-induced ROS could also inhibit cell growth by inducting apoptosis by activating a mitochondrial caspase pathway and preventing the activation of the VEGF-A-mediated PI3K/Akt pathway.
Our studies indicated that HY-PDT exhibited concentration-dependent photocytotoxic effect. As shown in Fig. 1b, both HY and haematoporphyrin (HP) showed the inhibitory effect on HUVECs; cell viability following the 2 μM HP-PDT was 81.0%, whereas that following the 0.125 μM HY -PDT was 38.5%. The IC50 value of HY was 0.067 μM, which was much less than that of HP (2 μM). It is worth noting that in the cell viability studies of HUVECs, no inhibition was found in Non-PDT groups, indicating that the inhibitory effect of HY or HP is light-dependent. HY displays negligible biological activity in the absence of light33.
Our studies revealed that the photocytotoxic effects of HY are resulted from the induced apoptosis, as seen from DAPI staining experiments (Fig. 2 and Supplementary Fig. 2S). We have observed the nuclear morphology of the treated cells changed in different extents, including chromatin condensation, marginalization and even DNA fragmentation, all of which are characteristics of apoptosis. In particular, when treated with 0.125 μM HY, the nuclei were collapsed, and the DNA was fragmented (Supplementary Fig. S2a). This effect was further validated by flow cytometry. It was also observed that HY- or HP-PDT-treated cells displayed phosphatidylserine exposure (Annexin V+/PI–), a hallmark of early apoptosis. Furthermore, the number of late apoptotic or necrotic cells (Annexin V+/PI+), which are characterized by plasma membrane damage, significantly increased. This explained why DNA fragmentation was only observed with the highest concentration of HY (0.125 μM). Additionally, excess ROS was detected, which is associated with apoptosis, as ROS promotes mitochondrial toxicity and macromolecular membrane damage, and consequently DNA fragmentation19,34,35. Thus, it is evident, that the excess ROS in mitochondria contribute to the mitochondrial caspase apoptotic signalling pathway19,36,37. Hence, we concluded that HY-PDT induces apoptosis by facilitating ROS production.
Importantly, our findings also revealed that the treatment with HY-PDT significantly increased the production of the inflammatory factors, including TNF-α and IL-6 (Fig. 3). These inflammatory factors are primarily modulated via intracellular ROS38,39. TNF-a, IFN-γ and IL-6 have been shown to be important in the promotion of an efficient innate immune response. Thus, our findings showing a remarkable increase in TNF-α, IL-6 and IFN-γ expression is consistent with a pro-inflammatory state involving the up-regulation of the innate immune system. Notably, the expression of the IL-6 mRNA and protein was more significantly up-regulated. IL-6 provokes specific cellular immune responses to inflammatory stimuli and also activates thymic lymphocytes (T-cells)40. However, HY-PDT did not affect the production of IL-1β or the immunosuppressive factors IL-10, suggesting that HY-PDT could promote the secretion of inflammatory mediators in a cell-selective manner. Our studies reveal that the HY-PDT can activate cell death via activation of the inflammatory response, sequentially inducing TNF-a, IFN-γ and IL-6 secretion. Such a cascade event thereby suggest that an additional potential of HY-PDT to suppress cell growth over the long term.
Previous studies have revealed that the photodynamic action of HY primarily targeted the mitochondria41. Rapid depletion of the ΔΨm leads to changes in mitochondrial membrane permeability, which is regulated by the balance of the pro- and anti-apoptotic Bcl-2 family proteins42. Thus, an increased ratio of pro- and anti-apoptotic protein expression, namely, the Bax/Bcl-2 ratio, may lead to the loss of mitochondrial membrane potential, resulting in the release of cyto c. Subsequently, the downstream effectors, caspase-9 and caspase-3 are activated, and PARP is cleaved. Eventually apoptosis occurs. In this studies, we did observed all these events. Importantly, we have observed the pan-caspase inhibitor (zVAD-fmk) or the specific Bax inhibitor (BIP) can reduce the effects on above-mentioned apoptosis-associated factors. These results indicate that HY-PDT induces apoptosis undergoing a mitochondrial-mediated pathway.
Interestingly, we found that down-regulated VEGF-A, Akt and p-Akt proteins and up-regulated dephosphorylated Bad (Fig. 7). Furthermore, this could be rescued by the addition of VEGF-A (Supplementary Fig. 7S). Based on these results, we concluded that HY-PDT could inhibit HUVEC growth by preventing the activation of the VEGF-A-induced PI3K/Akt pathway, which was initiated by the suppression of VEGF-A expression and subsequent down-regulation of the levels of the total Akt and p-Akt proteins, and eventually stimulating the Bad dephosphorylation43. Bad is a critical pro-apoptotic protein of the Bcl-2 family of proteins and is reportedly able to promote the release of cyto c to activate caspase-dependent apoptosis44. Putting all the data together, we concluded that HY-PDT could induce apoptosis by activating the mitochondrial caspase pathway and by inhibiting the VEGF-A-mediated PI3K/Akt pathway. These are alternative mechanisms to inhibit cell growth. However, PDT is an oxygen-consuming modality. In an adaptive response to the hypoxic stress, the cells might trigger angiogenesis by immediate up-regulating pro-angiogenic factors, such as VEGF45. Our observation of decreased VEGF-A expression at 24 h following PDT can likely be explained that reoxygenation occurred after 24 h following the HY-PDT treatment46.
In conclusion, our study demonstrated that HY can inhibit the cell growth and induce apoptosis in HUVECs; HY also exhibits more potent effects than HP in the PDT. Our studies further discovered a novel mechanism of cell death underlie the role of HY. HY can promote the production of cytotoxic ROS, leading to cell death and the activation of the inflammatory responses. Furthermore, HY can also induce apoptosis by activating the mitochondrial caspase pathway and inhibiting the activation of the VEGF-A-mediated PI3K/Akt pathway. Taken together, HY should represent an excellent alternative to HP in PWSs treatment, owing to its shorter half-life yet higher photocytotoxic effects at lower concentrations.
How to cite this article: Zhang, Q. et al. Hypericin-photodynamic therapy induces human umbilical vein endothelial cell apoptosis. Sci. Rep. 5, 18398; doi: 10.1038/srep18398 (2015).
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Multi-OMIC profiling of survival and metabolic signaling networks in cells subjected to photodynamic therapy
Cellular and Molecular Life Sciences (2017)