乌骨藤提取物对人红细胞的毒性研究

Cytotoxicity of anti-tumor herbal Marsdeniae tenacissimae extract on erythrocytes 乌骨藤提取物对人红细胞的毒性研究 1 first-author 1 1 1 2 1 1 1 1 1 1 corresp ‡Corresponding Authors ‡Corresponding Authors †E-mail:mmizjpph89@163.comzhenwangzjpph@163.com †E-mail:mmizjpph89@163.comzhenwangzjpph@163.com mmizjpph89@163.com 1 corresp ‡Corresponding Authors ‡Corresponding Authors †E-mail:mmizjpph89@163.comzhenwangzjpph@163.com †E-mail:mmizjpph89@163.comzhenwangzjpph@163.com mmizjpph89@163.com Research Center of Blood Transfusion Medicine, Ministry of Education Key Laboratory of Laboratory Medicine, Department of Blood Transfusion, Zhejiang Provincial People’s Hospital, People’s Hospital of Hangzhou Medical College, Hangzhou 310014, China Research Center of Blood Transfusion Medicine, Ministry of Education Key Laboratory of Laboratory Medicine, Department of Blood Transfusion, Zhejiang Provincial People’s Hospital, People’s Hospital of Hangzhou Medical College, Hangzhou 310014, China Department of Blood Transfusion, Lishui People’s Hospital, Lishui 323000, China Department of Blood Transfusion, Lishui People’s Hospital, Lishui 323000, China Marsdeniae tenacissimae extract (MTE) has been used as an adjuvant medicine for cancer therapy for a long time. Although massive studies demonstrated its considerable anti-cancer effect, there is no research on its influence on erythrocytes, which are firstly interacted with MTE in the circulation. To investigate the influence of MTE on erythrocytes, we used a flow cytometer to detect the MTE-treated alternations of morphology, calcium concentration, and reactive oxygen species (ROS) level in erythrocytes. We used hemolysis under different osmotic solutions to evaluate the fragility of erythrocytes. Data showed that MTE treatment dose-dependently increased the ratio of erythrocyte fragmentation ( P < 0.001) and shrinking, and elevated the forward scatter (FSC) value ( P < 0.001) and calcium accumulation ( P < 0.001). MTE induced ROS production of erythrocytes under the high glucose condition ( P < 0.01) and consequently caused a rise in fragility ( P < 0.05). These results suggest that MTE induces cytotoxicity and aging in erythrocytes in a dose-dependent manner, and presents the possibility of impairment on cancer patients’ circulating erythrocytes when MTE is used as an anti-cancer adjuvant medicine. 目的 2 评估乌骨藤提取物对红细胞形态及生理功能的影响，并初步探讨其作用机制。 创新点 2 首次检测乌骨藤提取物对红细胞的毒性作用，并且初步探索此毒性作用与乌骨藤导致的红细胞内活性氧（ROS）和钙离子水平的相关性。 方法 2 不同浓度乌骨藤提取物（0、64、128和256 µg/ml）处理红细胞24 h，通过流式细胞术检测前向角散射（FSC）和侧向角散射（SSC），计算红细胞破碎率和大小改变，通过显微镜观察形态学的变化；装载2’,7’-二氯荧光黄双乙酸盐（DCFH-DA）和钙荧光探针Fluo-4染料，通过流式细胞术分别检测红细胞ROS和钙离子荧光强度的变化；通过观察一系列低渗生理盐水下红细胞的溶胀情况，评估乌骨藤提取物对红细胞脆性的改变。 结论 2 乌骨藤提取物剂量依赖性地增加红细胞的破碎率（图1），导致FSC增加（图2），同时高浓度乌骨藤提取物（256 µg/ml）导致红细胞圆盘状结构消失（图3）；128和256 µg/ml乌骨藤提取物处理红细胞导致胞内钙离子显著增加（图4）；乌骨藤提取物在高糖环境中诱导红细胞ROS累计，并最终导致红细胞脆性增加（图5）。上述结果显示，乌骨藤提取物对红细胞有毒性作用，并有可能在临床抗癌治疗中破坏红细胞引起潜在的毒副作用（图6）。 Marsdeniae tenacissimae extract Erythrocyte Calcium Reactive oxygen species (ROS) Fragility 乌骨藤提取物 红细胞 钙离子 活性氧（ROS） 红细胞脆性 Introduction 1 In recent decades, traditional herbal medicine has been increasingly used in anti-tumor therapy as an enhancement of radiation therapy and chemotherapy. The plant Marsdeniae tenacissimae , belonging to the section asclepiadaceous, has been used as a folk medicine for thousands of years in China. In clinical terms, it plays an immunoregulation role in asthma, trachitis, tonsillitis, pharyngitis, pneumonia, and rheumatism (Ye et al., 2014a 2014a ; Zhu et al., 2014 2014 ; Fan et al., 2015 2015 ). Additionally, M . tenacissimae extract (MTE) has long been used as an adjuvant medicine for cancer therapy (Han et al., 2012 2012 ; 2014 2014 ). Using the water extract of M . tenacissimae , Xiao-Ai-Ping injection has been approved by China Food and Drug Administration (CFDA) for antitumor therapy (Huang et al., 2013a 2013a ). A number of recent studies suggested that MTE treatment alone presented a distinctive effect against various cancers, including gastric cancer, esophageal cancer, lung cancer, and hepatocellular carcinoma, through suppressing proliferation and promoting apoptosis of cancer cells (Huang et al., 2013a 2013a ; 2013b 2013b ; Li et al., 2015 2015 ). Previous research in our lab showed that the inhibition of MTE on tumor angiogenesis depended on the attenuation of vascular endothelial growth factor (VEGF) and VEGF receptor 2 (VEGFR2) interactions and the protein kinase C pathway in vein endothelial cells (Chen et al., 2016 2016 ). Currently, most studies on MTE focus on its anti-tumor effect, but no information is available about its influence on blood cells, which are firstly interacted with MTE in the circulation after its injection. Erythrocytes are the largest in the number of blood cells with the principal function of delivering oxygen to the body tissues. Mature erythrocytes are flexible and oval biconcave disks, without a cell nucleus, mitochondria, or most organelles, in order to accommodate maximum space for hemoglobin (Ellsworth et al., 2009 2009 ; Pretorius et al., 2016 2016 ). Some traditional medicine-induced apoptosis and suicidal erythrocyte death have been reported (Lupescu et al., 2012 2012 ; Zelenak et al., 2012 2012 ; Bouguerra et al., 2015 2015 ). However, other compounds, such as salidroside, protected erythrocytes against oxidative stress and apoptosis (Qian et al., 2011 2011 ; 2012 2012 ; Shaik et al., 2012 2012 ). Because of the cytotoxicity of MTE on tumor cells, we supposed MTE might also induce biochemical and biophysical alterations in erythrocytes. In the current study, we address the influence of MTE on human erythrocytes and the underlying mechanism. To achieve this goal, we carried out comparative studies on erythrocyte size, integrality, reactive oxygen species (ROS), calcium content and hemolysis (fragility) after MTE treatment. Materials and methods 1 MTE and erythrocytes 2 MTE was extracted from the stem of M . tenacissimae as follows: the powder of M . tenacissimae stem was gained by extracting with water three times, followed by filtering and concentrating. The water extract was resuspended with 85% ethanol and centrifuged at 4 °C three times. Finally the ethanol extract was lyophilized and resuspended at 500 μg/ml in DMSO (Sigma, St. Louis, MO, USA). Fresh leukocyte-reduced erythrocytes (within 5 d after donation) were kindly provided by the Blood Transfusion Department of Zhejiang Provincial People’s Hospital, Hangzhou, China. Erythrocytes, before use, were washed three times in saline to remove the preservative. Then the erythrocytes were suspended and incubated in RPMI 1640 media (Invitrogen, Carlsbad, CA, USA) at a hematocrit 0.5% with indicated glucose and MTE concentrations at 37 °C for 24 h. Forward scatter and side scatter analysis 2 After incubation in RPMI 1640 media containing 0, 64, 128, and 256 μg/ml MTE for 24 h, 200 μl erythrocyte solutions were suspended in fresh media and analyzed for forward scatter (FSC) and side scatter (SSC) using a flow cytometer (FACS, ACEA NovoCyte, San Diego, CA, USA). Fresh washed erythrocytes were used to determine the integral ranges of FSC and SSC for calculating the integrity rate. ROS analysis 2 Erythrocytes were incubated in RPMI 1640 media with different levels of glucose (2.8, 5.6, and 11.1 mmol/L) and MTE (0, 64, 128, and 256 μg/ml) for 24 h, and then immediately loaded with 2 mmol/L ROS fluorescent dye 2',7'-dichlorofluorescin diacetate (DCFH-DA; Beyotime, Peking, China) for 20 min at 37 °C. The fluorescence intensity of the erythrocytes was measured in the FACS device with excitation 488 nm and emission 530 nm. Calcium analysis 2 The erythrocytes were treated with different levels of MTE (0, 64, 128, and 256 μg/ml) for 24 h, and then immediately loaded with 1 μmol/L calcium fluorescent dye Fluo-AM (Molecular Probes, Eugene, OR, USA) for 20 min at 37 °C. The fluorescence intensity of the erythrocytes was measured by the FACS device with excitation 488 nm and emission 530 nm. Erythrocyte osmotic fragility 2 Erythrocyte fragility was examined in different amounts of NaCl solution (pH 7.4) from 0.0% to 0.9% (1%=0.01 g/ml). Briefly, after 24 h treatment with MTE, erythrocytes were carefully suspended in various concentrations of NaCl and incubated for 2 h at 4 °C. Subsequently, the test tubes were centrifuged at 600 g , and the supernatant was collected for hemolysis measurement via 540 nm absorbance using a microplate reader (Tecan, Männedorf, Switzerland). The percentage of hemolysis was normalized by pure water hemolysis supernatant. Statistics 2 All data are presented as mean±standard deviation (SD) and were analyzed using Student unpaired two-tailed t -test and one-way analysis of variance (ANOVA) with Tukey post-hoc test (GraphPad Prism 6 software). P < 0.05 was considered significant. Results 1 MTE treatment decreased the normal integrated erythrocyte ratio 2 To investigate the influence of MTE on erythrocytes, we first tested the number alternation of erythrocytes after MTE treatment. MTE treatment showed a dose-dependent reduction on the ratio of integrated erythrocytes, which were defined by fresh erythrocytes (Fig. 1 1 ). Meanwhile small fragments of erythrocyte were much increased after 256 µg/ml MTE treatment, and a typical result is shown in Fig. 1a 1a . (a) The decreased ratio of normal erythrocyte after 256 μg/ml MTE treatment (red) compared with untreated (gray). (b) Various concentrations of MTE decreased the integrated erythrocyte ratio gradually. Data are expressed as mean±SD ( n =3). * P < 0.05, *** P < 0.001 vs. control group (no MTE) (Note: for interpretation of the references to color in this figure legend, the reader is referred to the web version of this article) MTE elevated FSC but reduced SSC of erythrocytes 2 To explore the effects of MTE on the size and granularity of erythrocytes, the FSC and SSC of erythrocytes were detected by a flow cytometer. Incubation in 256 µg/ml MTE for 24 h significantly increased the FSC level as shown in Fig. 2a 2a . A more detailed experiment showed MTE dose-dependently elevated erythrocyte FSC level, in which 256 and 128 µg/ml but not 64 µg/ml MTE have a significant increase (Fig. 2b 2b ). Meanwhile, the SSC level of erythrocytes gradually decreased with increasing MTE concentration (Fig. 2c 2c ). Under the microscope, normal erythrocytes appeared as an oval biconcave disk (Fig. 3a 3a ). However, low concentration of MTE (64 and 128 µg/ml) treatment induced much more bending of the cell (Figs. 3b and 3c 3b and 3c ). High dosage of MTE resulted in cell shrinking and the presence of irregular, or even absence of, concave characteristic (Fig. 3d 3d ). (a) 256 μg/ml MTE induced a higher FSC level of erythrocytes. (b) Various concentrations of MTE increased the FSC level of erythrocyte gradually. (c) Various concentrations of MTE decreased the SSC level of erythrocyte. Data are expressed as mean±SD ( n =3). * P < 0.05, ** P < 0.01, *** P < 0.001 vs. control (Ctrl) group (no MTE) (a) Control; (b) 64 μg/ml MTE; (c) 128 μg/ml MTE; (d) 256 μg/ml MTE. Bar=20 μm MTE treatment induced erythrocytes’ calcium accumulation 2 To investigate the underlying mechanism of erythrocytes’ shape alternation and eryptosis, their calcium concentrations were measured by Fluo-4 fluorescence. Erythrocytes’ calcium influx is an important trigger of eryptosis, and is dramatically induced by 256 µg/ml MTE (Fig. 4a 4a ). Further experiments revealed that the higher the concentration of MTE treated, the more calcium accumulated in erythrocytes (Fig. 4b 4b ). Counting the ratio of erythrocytes with high calcium content (fluorescence value > 1000) also showed the same result, i.e. that the calcium cell ratio was markedly increased after MTE treatment (Fig. 4c 4c ). (a) 256 μg/ml MTE stimulated calcium accumulation in erythrocytes. (b) Various concentrations of MTE increased the calcium level of erythrocytes gradually. (c) Otherwise various concentrations of MTE induced a high ratio of calcium-accumulated erythrocytes (calcium fluorescence > 1000). Data are expressed as mean±SD ( n =3). * P < 0.05, ** P < 0.01, *** P < 0.001 vs. control (Ctrl) group (no MTE) MTE treatment stimulated erythrocyte ROS production in high glucose condition 2 To reveal the relation between MTE and erythrocyte ROS production, the erythrocytes were loaded with DCFH-DA after MTE incubation. Under a normal glucose condition (5.6 mmol/L), 128 and 256 µg/ml MTE markedly stimulated ROS production (Fig. 5a 5a ), and 2.8 mmol/L glucose attenuated the increasing effect of 128 µg/ml MTE. However, 11.1 mmol/L glucose enhanced the effect of 64 µg/ml MTE, leading to evident ROS elevation (Fig. 5a 5a ). ROS is one of the byproducts of aerobic metabolism, and would damage erythrocytes. Therefore, we examined erythrocyte FSC under different glucose conditions. The data showed that the FSC level has the same results as ROS (Fig. 5b 5b ), which suggested the influence of MTE on erythrocyte ROS and FSC depended on a high glucose metabolism. (a) ROS in erythrocytes was more induced by MTE under high glucose (11.1 mmol/L) environment than under low glucose (2.8 mmol/L). (b) FSC levels of erythrocytes were much more stimulated by MTE under high glucose environment than under low glucose. Data are expressed as mean±SD ( n =3). * P < 0.05, ** P < 0.01 vs. control group (no MTE) for each glucose concentration MTE induced high erythrocytes’ fragility 2 To investigate the erythrocytes’ fragility, we tested the hemolysis under different osmotic solutions. Fig. 6 6 shows that low osmotic solution induced severe erythrocyte hemolysis, and under 0.40%‒0.45% NaCl concentrations MTE-treated erythrocytes presented a high hemolysis ratio, which implicated that MTE induced erythrocyte impairment and a greater sensitivity to decreasing osmosis. MTE treatment induced a high hemolysis ratio under 0.40%‒ 0.45% NaCl solutions (1%=0.01 g/ml). Data are expressed as mean±SD ( n =3). * P < 0.05 vs. untreated group Discussion 1 In China, M . tenacissimae has already been used in asthma, trachitis, tonsillitis, pharyngitis, pneumonia, and rheumatism as an immunoregulator (Ye et al., 2014a 2014a ; Zhu et al., 2014 2014 ; Fan et al., 2015 2015 ). In recent decades, M . tenacissimae water extract Xiao-Ai-Ping has been approved by CFDA and used as an adjuvant medicine for cancer therapy in China (Huang et al., 2013a 2013a ). Studies have reported that MTE could decrease the proliferation and increase the apoptosis of hematologic neoplasm tumor cells both in vitro and in vivo (Ye et al., 2014a 2014a ). At the same time MTE showed an obvious enhancement on gefitinib-induced anti-cancer efficacy via prompting cell cycle arrest and apoptosis and suppression of the activation of epidermal growth factor receptor (EGFR) and c-Met in both EGFR mutant and wild-type non-small cell lung cancer cells (Han et al., 2012 2012 ; 2014 2014 ). Our lab previously revealed the strong anti-proliferation effect of MTE on human vein endothelial cells due to the attenuated VEGF/VEGFR2 interactions and promoted apoptosis through p53-dependent mitochondrial pathway (Chen et al., 2016 2016 ). Because of the marked cytotoxicity of MTE, we speculated that it might have the same or even more serious impairment on erythrocytes, which are firstly interacted with MTE in the circulation. However, there was no report about the influence of MTE on erythrocytes. Erythrocyte is the unique cell for delivering oxygen to the body tissues. Its damage may cause a series of symptoms of tissue hypoxia (Tziakas et al., 2012 2012 ). It has been shown that other adjuvant anti-cancer medicines, such as gambogic acid and tanshinone IIA, impaired erythrocytes via shrinking, reduction of ATP, and promotion of apoptosis (Lupescu et al., 2012 2012 ; Zelenak et al., 2012 2012 ). Salidroside, naringin, and cisplatin, on the other hand, have a protective effect through inhibiting ROS production and calcium influx (Qian et al., 2011 2011 ; 2012 2012 ; Shaik et al., 2012 2012 ; Yang et al., 2015 2015 ). In this study, we elucidated the impairment of MTE on erythrocytes’ quantity and appearance (Figs. 1 1 ‒3). After MTE treatment, the ratio of integral erythrocyte was reduced while increased FSC suggested the alternation of erythrocyte in shape (Fig. 2 2 ). Observation under microscope confirmed that change of erythrocytes that lost the oval biconcave disks after exposure to MTE (Fig. 3 3 ). Consequently, the MTE-induced change of erythrocytes in shape led to a greater sensitivity and higher fragility to decreasing osmosis (Fig. 6 6 ). To investigate the underlying mechanism of MTE on eryptosis, we further examined calcium accumulation and ROS production of erythrocytes after MTE treatment. Due to the lack of mitochondria and nuclei, eryptosis is unregulated by mitochondria dysfunction and gene expression. Indeed, calcium influx activates Ca 2+ -sensitive K + channels, cell shrinkage, and membrane scrambling, then triggers erythrocyte aging and eryptosis (Maher and Kuchel, 2003 2003 ; Bogdanova et al., 2013 2013 ). MTE-treated erythrocytes showed a high average calcium concentration (Fig. 4b 4b ) and an increasing ratio of high-calcium cells (Fig. 4c 4c ), and these may contribute to the acute erythrocyte decline (Fig. 1 1 ) and chronic erythrocyte aging as demonstrated by high erythrocyte fragility (Fig. 6 6 ). ROS is another important injury factor. In erythrocytes, because of a deficiency of mitochondria, ROS is mainly produced by cytosolic aerobic oxidation and auto-oxidation during oxygen delivering (Abed et al., 2014 2014 ; Lang et al., 2014 2014 ). A high level of ROS will interrupt the cell membrane lipid and cell cytoskeleton, and consequently impair the normal erythrocyte shape (Ziobro et al., 2013 2013 ). Our data showed that 24 h MTE incubation induced high ROS production (Fig. 5 5 ) in erythrocytes. Experiments of different glucose levels revealed that erythrocyte ROS and FSC were higher as the glucose concentration level increased (Fig. 5 5 ), which suggested that metabolism-dependent ROS production may be the major reason for the rise in FSC and shape alteration. MTE, in our experiments, was a crude extract containing abundant C 21 steroids with anti-cancer activity, which have been previously extracted from several kinds of herbal medicine and have presented cytotoxicity in various cancer cell lines (Li et al., 2016 2016 ; Yin et al., 2016 2016 ). From M . tenacissimae , more than 40 kinds of C-21 steroidal glycosides have been isolated (Zhang et al., 2010 2010 ). Tenacissoside C, a natural bioactive compound of C-21 steroidal saponins, was purified from M . tenacissimae and exhibited a marked anti-tumor effect on the myelogenous leukemia cell line (Ye et al., 2014b 2014b ). In contrast, another important component of Xiao-Ai-Ping injection, such as 17β-tenacigenin B, had no significant anti-tumor effect in vitro (Wang et al., 2015 2015 ). Therefore, we have strong hopes to reveal the possible compounds causing the erythrocyte impairment and try to attenuate this adverse effect in future research. Conclusions 1 In this study, we found MTE-induced dose-dependent cytotoxicity and aging in erythrocytes. MTE treatment increases the ratio of erythrocyte fragmentation and shrinking, elevates the calcium and ROS levels, and consequently causes increased fragility. These findings suggest a possible impairment on cancer patients’ circulating erythrocytes when the Xiao-Ai-Ping injection is used as an anti-cancer adjuvant medicine. Contributors 2 Ke HAO and Bing-yu CHEN equally contributed to the experimental research, data analysis, and writing and editing of the manuscript. Kai-qiang LI and Yu ZHANG contributed to the experimental research. Cai-xia LI and Ying WANG contributed to the writing and editing of the manuscript. Lu-xi JIANG and Jiang SHEN contributed to the fragility test. Xiang-chai GUO and Wei ZHANG contributed to the study design and data analysis. Meng-hua ZHU and Zhen WANG contributed to the study design, data analysis, and writing and editing of the manuscript. Meng-hua ZHU and Zhen WANG are the guarantors of this work and, as such, had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. References M Abed , F Artunc , K Alzoubi , 等 . Suicidal erythrocyte death in end-stage renal disease . J Mol Med , 2014 . 92 ( 8 ): 871 - 879 . 24743961 DOI: 10.1007/s00109-014-1151-4 http://doi.org/10.1007/s00109-014-1151-4 . 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LQ16H070003, LY15H280010, and LY15C090004), the Key Project of Chinese Medicine in Zhejiang Province (No. 2015ZZ001), the Traditional Chinese Medicine Scientific Research Foundation of Zhejiang Province (No. 2014ZB007), the Traditional Chinese Medicine Outstanding Young Talent Foundation of Zhejiang Province (No. 2014ZQ005), and the Medicine and Health Research Foundation of Zhejiang Province (No. 2015ZDA002), China 2016-05-19 2017-06-07 2016-06-20 2022-01-05 Copyright © Zhejiang University and Springer-Verlag Berlin Heidelberg 2017 2017 Journal of Zhejiang University-SCIENCE B (Biomedicine and Biotechnology) 07 18